Open access peer-reviewed chapter

Breast and Cervix Uteri: Rare Locations for Mycobacterium Tuberculosis Infections and Complications-Cases Report and Literature Review

By Manuela Cristina Russu, Şerban Nastasia, Daniela Degeratu and Ruxandra Viorica Stănculescu

Submitted: October 31st 2017Reviewed: February 7th 2018Published: September 26th 2018

DOI: 10.5772/intechopen.75044

Downloaded: 730


Breast and cervix uteri are rare locations for Mycobacterium tuberculosis (MbT) infection and MbT association to cervical cancer is more rare in European countries. This chapter analyses two cases of rare locations of tuberculosis (TB) in young Romanian women. The first patient presented a chronic primary TB breast abscess, non-pregnancy related with periods of apparent healing and repeated areolar fistula formation. In the second case, the unexpected discovery of secondary TB endocervical granulomatous inflammation with caseous necrosis on a radical hysterectomy specimen, performed after chemoradiotherapy for squamous non-keratinizing cell carcinoma is presented. Worldwide incidence, risk factors, hypothetic mechanisms of primary/secondary breast and cervix uteri MbT infection, the association to high-risk HPV, microbiological diagnosis difficulties, the differentials to pyogenic abscesses, other chronic granulomas and breast cancer treatment issues are presented in the reviewed literature, focusing on the peculiarities of these rare locations and complications. It is recalled an old concept of “therapeutic antitubercular” test when all other assessments steps are usefulness.


  • tuberculosis
  • breast abscess
  • cervical caseous granuloma
  • carcinoma

1. Introduction

Tuberculosis (TB) is an old disease, known since 5000BC, and contemporary professional and scientific communities are challenged by the WHO’s “Global Tuberculosis Report 2017”showing 6.3 million new cases of TB in 2016, with about 16% expected to die due to TB by 2020. These data may be connected to the lack of an effective vaccine, and of sensitive and rapid diagnostic tests, to the appearance of multidrug resistant strains of Mycobacterium tuberculosis(MbT) [1, 2]. Low income, immunosuppressive disorders, worldwide travels and immigration are associated to TB globalization [3]. Breast and uterine cervix are rare locations for MbTeven in TB endemic countries [1]. This chapter analyses two cases of rare locations of TB in young women from Romania, a middle-income country. The first case is a chronic, non-pregnancy-related primary breast abscess, with areolar fistula formation between periods of apparent healing. The second case is an association of secondary endocervical tuberculosis to a squamous cervical carcinoma in a young woman with a previous lung tuberculosis, without activation during/after specific cervical cancer therapy. In Europe, there are few papers in the form of case reports on breast or cervix uteri tuberculosis. Breast and cervix uteri tuberculosis are uncommon diseases with non-specific clinical, imagistic and or cytological/histological findings. Misdiagnosis or the diagnosis after many negative assessments for these rare TB locations are common, because biopsy specimens are paucibacillary, and other investigations such as microscopy and culture are frequently negative, as it is the PCR for MbT. MbTcan simulate cervical carcinoma in premenopause and postmenopause [4, 5] due to abnormal vaginal bleeding at clinical presentation.

We intent to review and refresh the theories/hypothesis on the epidemiology, pathophysiology, diagnosis and therapeutic issues on these rare MbTlocations and complications. In countries like Romania, where TB is non-endemic and the diagnosis for extra pulmonary tuberculosis is a surprise, the golden standard of microbiological evidence of MbTis rare, even with the new molecular techniques. It is reconsidered the “old concept of the therapeutic test” with antitubercular drugs, which was proved to be active in pulmonary tuberculosis.


2. Cases presentation

First case:A 31 years old Caucasian woman, higher studies and salaried, married, nuligesta, on combined oral contraceptives, no family or personal history of tuberculosis or known exposure to a person with tuberculosis, no mammary surgery, is presenting in December 2014 with nipple retraction and inversion, skin redness and thickening, over a breast inflammatory tumor of 2 x 1 cm size, in the internal upper quadrant of the right breast, freely mobile and a fistula at areola level, with no axillary or cervical lymphadenopathy, and normal left breast. The systemic examination is non-contributory, and no associated constitutional symptoms, as fever, no weight and appetite loss are registered.

The patient had three previous similar episodes, since 2007, with a fistula of the right breast abscess, sterile cultures for aerobic/anaerobic germs, and yeasts in the nipple purulent discharge.

Routine hematological and biochemical investigations, and serum prolactin levels are normal, HIV test is negative. Breast sonography reveals skin thickening, nipple retraction and dilated terminal ducts and ill-defined thick-walled cystic mass of 2.9 cm diameter.

The cytological examination after Giemsa stain from the fistula’s purulent discharge shows a rich cellular smear, with many polymorphs background, lymphohistiocytic aggregates and Langhans type multinuclear giant cells, fibrin debris and rare epithelial cells, which conducted to the conclusion of a chronic breast inflammatory granuloma.

It is decided and incision-excision of the inflammatory mammary gland tissue was performed, with large drainage of the remaining cavity, samples collection for pathology/microbiology and no other unwanted events as shock or toxemia.

In January 2015, a new fistula occurred on the opposite on the opposite area of the right nipple, with discharge of purulent material, without fever or other general symptoms, as she never presented at each previous medical consultations (Figure 1).

Figure 1.

Photograph of the scar from slowly-healing post-incision/excision-drainage wound of the right breast, and the new fistula on the opposite part of the right areola and purulent discharge.

The cultures for aerobic/anaerobic germs and yeasts are sterile, the pathological examination discovers rare epithelial cells of squamous type, lymphocytes, plasma cells, histiocytes, multinuclear giant cells of Langhans type and a multitude of blood vessels. The Ziehl Neelsen stain for acid-fast bacilli and PCR for MbTfrom sample collected at excision biopsy are negative (Figure 2(A, B)).

Figure 2.

Pathological images (A.Hematoxylin & Eosin, 40X;B.Hematoxylin & Eosin, 20X): Inflammatory granulomatous lesions: Rich chronic inflammatory infiltrate, with many histiocytes (with epithelioid aspect) and frequent multinuclear giant cells Langhans-type. Collection of Degeratu Daniela, “Dr I. Cantacuzino” Laboratory of Pathology.

The chest X-ray examination is normal and the PPD skin test is 10 mm.

In March 2015, a 6 months antitubercular treatment (ATT) with three drugs was recommended: isoniazid, rifampicin and ethambutol with intensive therapy for the first 3 months is administered. The follow up from May 2015 (after 2 months of intensive therapy) shows remission of the fistulas, heal of the skin, the persistency of the nipple retraction and a 2 kg weight gain. The patient had a total 9 months ATT (Figure 3).

Figure 3.

Photograph of the right breast after two months of intense active antitubercular treatment. Patient in recumbent position with healed wound, without sinuses of the areola, and inverted nipple.

The final diagnosis is primary non-gestational breast tuberculosis abscess.

The second case: A 29 years merchandise by occupation, smoker of five cigarettes per day, non-alcoholic, married since 10 years is presenting for repeated postcoital abnormal vaginal bleeding and blood-stained discharge since 6 months. History: physiology: the menarche: 14 years; 2 full-term spontaneous deliveries; 1 abortion; pathology: pulmonary tuberculosis (treated and considered healed in 2002); no surgical illness. LMP: August 20, 2008, immunological pregnancy and HIV tests: negative. General physical examination was essentially normal; abdominal examination revealed no mass, no ascites, no hepatosplenomegaly and no other abnormality.

Vaginal speculum examination: an irregular, cauliflower-like tumor of 4 cm in the largest size on the anterior cervical ridge, spontaneously bleeding, and on touch; normal vaginal walls and bilateral fornices.

Vaginal bimanual examination: anteverted uterus of normal shape, and volume, firm, mobile and no adnexal mass.

Per-rectal examination: smooth rectal mucosa, and freely mobile, no induration or nodularity of both parametrials.

Pap smear: epithelioid-like cell clusters with atypia. Colposcopic examination increased vascularity on the posterior cervical ridge, acetowhite on the anterior cervical ridge, with negative iodine stain with precise contour around the previously described cauliflower-like tumor.

Provisional diagnosis of carcinoma cervix stage I B was kept, and after preliminary investigations, patient was posted for multiple cervical biopsies—the tumor and from other four cardinal points in the vicinity.

The histopathological diagnosis came out to be squamous non-keratinizing cell carcinoma (Figure 4), and the specific tests for viral infection had revealed the presence of genotype 33 HPV.

Figure 4.

Two confluent epithelioid caseous granulomas with Langhans-type gint multinuclear cells and lymphocytic inflammatory infiltrate at the periphery, HE stain, 10 x. Collection of Degeratu Daniela, “Dr I. Cantacuzino” Laboratory of Pathology.

Hematological test: low degree anemia (Hb: 11.0 mg/dL, Ht; 34%), leukocytosis and thrombocytosis.

Biochemical and coagulation tests: normal.

Chest radiography showed fibrous and fibro-nodular sequelae of pulmonary tuberculosis.

After 4 weeks of radiotherapy (tele-radiation and 2 cures of brachytherapy) plus chemotherapy (cisplatin), the patient is proposed for surgery, which is accepted and it is done a Wertheim’s radical hysterectomy with bilateral pelvic node dissection. The post-surgery pathological examination showed a cervix with large areas of ulceration, polymorph inflammatory infiltrate and multinuclear giant cells of foreign body type, micro-calcifications and small islands of squamous non-keratinizing cancer cells. The endocervix presents a granulomatous inflammation with caseous necrosis and Langhans multinuclear giant cells. The vaginal part and the lateral part of the cervix have no neoplastic invasion. The endometrium is atrophic, the ovaries have albicans bodies, the tubes have hypoplastic mucosa,and the examination of 10 lymphnodes shows their reactive aspect, lipo-dystrophy and micro-calcifications.

PCR for MbTwas performed on archived tissue (formalin-fixed paraffin embedded uterine tissue) following detection of cervical TB by pathology, was positive in the cervix. The patient has a normal evolution post-radio, chemotherapy and post-surgery, without any reactivation of the pulmonary tuberculosis.


3. Epidemiology: risk factors

3.1. Epidemiology of breast tuberculosis

Breast TB was first described in a very young woman by Sir Astley Cooper in 1829 as “scrofulous swelling of the bosom”, and the location of MbTin the cervix uteri was first described 2 years later by Renaud (1831). Extrapulmonary TB was reported in nearly 18% of cases in USA [6], and TB location in the breasts is extremely rare in Western populations from 0.025 to 0.1% of all surgically treated breast diseases. In the last 20 years, the Southern European countries such as Greece, Turkey, Italy and Spain reported rare such cases, and 0.64–3.59% of all mammary treatable conditions are in developing countries from Asia [7], where the overall incidence of histological confirmed breast TB is 0.4% per year [8]. In India, the incidence of breast TB is five times less common than carcinoma of the breast [8]. There are described fluctuations in the incidence of generally breast TB, with the highest incidence in Southern Turkey in 2007 [10], and in the last 8 years (Table 1) the reported cases with primary breast TB have an increasing incidence all over the world, as it is the Romanian case, which had the first episode in 2007. Mammary involvement is nearly equal in frequency in the right and left (40.0 vs. 44.0%) [10], bilateral disease is rare [11, 12], as it is the infra-mammary location of tuberculosis [13]. Breast tuberculosis is affecting women in the reproductive age, 21–30 years, predominantly, a case being reported during pregnancy [14], and rarely in prepubescent [15] and elderly postmenopausal women [16], the last category being more affected in the early twentieth century, and in the last years it is discovered in women and men [17, 18]. None of the recognized risk factors (multiparity, lactation, trauma, past history of suppurative mastitis, breast surgery/breast reconstruction [19, 20], silicon breast introduction or AIDS [21] was present in the Romanian reported case.

ContinentNumber of cases since the year 2000 (00)
North America0000000000001
South America003
New Zeeland

Table 1.

Annual worldwide published cases with primary breast tuberculosis (last 16 years medical literature - Google scholar, Medline, web of science).

It, Italy; Gr, Greece; T, Turkey; Ch, China; R, Romania; Mo, Morocco; In, India; Tw, Taiwan; Ir, Iran; Br, Brasil; Mx, Mexico; Co, Columbia; US, United States of America.

3.2. Epidemiology of cervix uteri tuberculosis

In developing countries like India, TB is a major socioeconomic burden, afflicting 14 million people mostly in the reproductive age group (15–45 years). Regarding the genital tract, fallopian tubes are involved in almost all the cases of pelvic tuberculosis, endometrium in 50–60% and ovaries in 20–30% [22]. Cervical tuberculosis accounts for 0.1–0.65% of all cases of the disease and 5–24% of genital tract [23].


4. Pathophysiology

4.1. Pathophysiology of breast tuberculosis

The breast was considered an organ that offers resistance to the survival and multiplication of the tubercle bacillus [24], like other organs such as spleen, skeletal muscle or cervix uteri, and this property is one of the reasons for the uncommon diagnosis of breast TB, and in countries like India it is supposed that the breast TB is confused to carcinoma [25], or to a pyogenic breast abscess [26], or to other diseases [27], tubercular mastitis being a “great masquerader” [28]. In contrast to this quality, when breast is infected with MbT, it was proved that BRCA 1/2 network is suppressed during infection suggesting that breast cell proliferation suppression is a feature of Koch bacilli survival [29].

Breast TB is described to be primary or isolated, and secondary. The primary breast TB is appreciated when the breast infection is the only manifestation of the disease, no demonstrable tuberculous focus exists elsewhere in the body [30], and the infection is through abrasions or through the openings of the ducts in the nipple. Primary breast TB is rare in comparison to secondary to lung or extrapulmonary, and the authors consider that the Romanian case is among primary breast tuberculosis. The secondary type is appreciated when a pre-existing lesion is located elsewhere in the body. Secondary MbTcan spread by three routes such as hematogenous, lymphatic or directly from the primary location such as lung, pleura, ribs, mediastinum and articular lesions. It is supposed that the patient had acquired the MbTduring a plain long distance travel, some previous years ago, when she claimed the first episode of breast inflammation; extensive travels seem to be responsible for tuberculosis globalization, statement common to others’ physicians [3], which is an explanation for a primary men’s breast tuberculosis, as it the case of a 44 years old Lithuanian man living in UK [18]. In countries where TB is endemic, young lactating women are more prone to develop breast tuberculosis, being described an incidence that can vary in the limits of 7–33% [31, 32, 33]. All types of Mycobacterium spp., and other types of antigens or foreign bodies, as milk during pregnancy or lactational period, are met by a vigorous cell-mediated hypersensitivity reaction involving macrophages, epithelioid and giant cells, Th1 lymphocytes, and their cytokines, which are activated and are developing the granulomas [34].

In Romania, like in countries with endemic tuberculosis as India, Pakistan, China, Iran and Korea, tubercular infection is seen more frequent secondary to a tubercular focus such as lungs, pleura or lymph nodes, which very frequently actually may not be detected clinical or radiological [26]. The breast infection is acquired usually from lungs by many routes (hematogenous, lymphatic via tracheobronchial, paratracheal, mediastinal lymph trunks or internal mammary nodes), by spread from contiguous structures and by ductal infection [8]. MbTis affecting differently breast structures, according to route of contamination: the epithelium of the ducts (primary) or of the lobules (secondary) with loss of acinar structures; and the entire epithelial lining of the lobules is destroyed, caseating necrosis appearing in the center of the lesion, and the destructive mechanisms are progressing and involving the skin, which may ulcerate and create fistula/sinuses; in other cases, specially in elder women, the mechanisms of repair/restoration are developing excessive dense fibrous tissue.

4.2. Pathophysiology of cervix uteri tuberculosis: Hypothesis on the association to cervical cancer

Pelvic organs are infected from a primary focus, elsewhere in the body, most commonly from lungs, by hematogenous spread. The cervix may be infected, as a part of this process, by lymphatic dissemination from the infected tube, or by direct extension from the endometrium. It is discussed a cervical infection from the sexual partner/partners with tuberculous epididymitis, being discussed the increased risk when there are multiple sexual male partners, especially in China [35]. It is discussed a relative immunity of the cervix to MbTas it was shown previously for other organs, which is probably connected to the inability of the bacillus to penetrate the squamous epithelium of portiovaginalis, and to cervical mucus resistance, but in rare cases, cervical TB may be a primary infection, MbTbeing introduced by a partner with tuberculous epididymitis or other genitourinary disease [36], but the sexual partner of the reported patient was negative for pulmonary TB. It was suggested the role of the sputum used as a sexual lubricant [22].

In the nineteenth century, it was a controversy as whether tuberculosis and cancer can coexist in the same organ; Carl von Rokitansky (1855) was the first to propose the view that there is a definite antagonism between the two, meaning that tuberculosis and cancer cannot be present in the same organ, but after the influences of Votta J Paul work and through his own further experience, Rokitansky later changed his previous generally accepted view, and admitted that tuberculosis and carcinoma can coexist, but that this coexistence is rather rare. The Romanian report on this pathological association is done for its rarity in Europe, and to the best of authors’ knowledge, in the last 45–50 years, two similar cases in Romania (Iaşi) by Luchian et al. [37] and one case in Poland [38] are described. The question is whether tuberculosis is before cancer, or the presence of the viral infection made possible the secondary location of the MbT.The pathological exams of the reported case did not revealed extensive granulomatous reaction, or cancer metastases in the endometrium, tubes, ovaries and lymph nodes. Since many years from the first description of the association of these two life-threatening pathologies, host response as the basic mechanism of specific defense against infection and tumor factors that enable such a response are also discussed since long time [39], being not completely known/understood, they may benefit from the host’s previously compromised immunity: MbTand HPV can potentate each other.

The MbTis a facultative intracellular parasite that grows well in non-activated macrophages. When large numbers of these bacilli have grown intracellularly within such macrophages, a cytotoxic immune response, herein called tissue-damaging delayed-type hypersensitivity kills the macrophages, forming the caseous center of the tubercle, where the tubercle is surviving; such a delayed-type hypersensitivity was first described for the pulmonary tuberculosis [40], and this patient have suffered from pulmonary tuberculosis 7 years earlier. The progression of cervical dysplasias to invasive, lethal cervical cancers has been attributed to diverse factors such as immune, hormonal, and nutritional status, or co-infection with other sexually transmitted agents, supporting data being equivocal [41].

The contemporary professional societies are sure on primary immune defense system deficiency or incapacities to some infections, bacterial and viral, which were demonstrated in the systemic circulation and in some bodies locations – in the cervix uteri or in the breast. In North America [42], Western Europe [43, 44] and recently in China [45], it was proved the shifted balance between T helper 1 (Th1)-type and Th2-type cytokines in cervical dysplasia [42, 46], the involvement and increase of invariant natural killer T (iNKT) cells (which are in small number in condyloma acuminatum, in mild and moderate dysplasias [47]), and the cytokines production from cervical keratinotytes [48] the main targets of HPV infection as the stratified epithelium cells, and the main source of cytokines [49], as type I interferon (IFN)-γ, tumoral necrosis factor (TNF)-α, transforming growth factor (TGF)-α, interleukin-1 (Il-1), interleukin-6 (Il-6), interleukin −8 (Il-8) expressions are involved in immune system modulation (all of them being parts of innate immune system), in the evolution from persistent high-risk HPV-infected cells to the development of high-grade cervical intraepithelial neoplasia and cervical cancer, because the keratinocytes cannot destroy the fact high-risk HPV, and that may work also on MbTinfection evolution, and complications. Parallel to these conditions, it is the individual cellular system of defense [50], involved in early phases of infection [51, 52]. Flow cytometry is revealing an increased level of CD3+ T, CD + 4 cells [53, 54] among both epithelium and stromal layers of the cervical tissues, contributing to the suppression of local immunity. In conjunction to these details is the presence of the population of monocytes/macrophages in the endocervix, with increasing number in cervical high-grade lesions with the parallel decrease in Langerhans cells, in contrary to what occurs in non-infected tissues [55]. All these facts contribute to the escape of HPV to tissue innate and acquired immune system, which is also influenced by the viral epitopes E6 and E7 [56], and evolution from less invasive to more advanced invasive cervical HPV-induced carcinoma is associated to a higher number of T and B lymphocytes, macrophages and induced nitric oxide synthase-expressing cells in the peritumoral stroma, so cell migration being proportional to the progression of the lesion [54]. Some studies show that these high number of inflammatory cells and compounds may open the way to bacterial infections, being additional mediators [57].

Insertional mutagenesis by HPV is another proposed tumor-promoting mechanism, but recent studies have not supported this hypothesis [58]. No common, recurring genetic alterations that cooperate with HPV to promote cervical cancer progression have been identified since Harald Zur Hausen first identified HPV as the causal transmissible agent of cervical cancer nearly 40 years ago [59]. To the pressing question to the biological basis of cervical cancer progression which is to be resolved since long time, the discover of the loss of a major tumor supressor LkB1[60, 61] or somatically acquired mutations in this tumor supressor LKB1[62], which is considered to be similar to p53. When LKB1deficiency/mutations, a primary cervical tumor confined to the cervix at the time of diagnosis has a bad prognosis: early metastasis and patient death, after the initial diagnosis despite aggressive therapy including radiation treatment. These abnormalities were first discovered in connection to Peutz-Jeghers Syndrome [63] and pulmonary cancer [64]. The MbTwas proved to reduce host’s immunity to high-risk HPV types for cervical cancer. The Chinese study “Shanxi Province Cervical Cancer Screening Study I” [36] showed an increasing magnitude of effect of MbTwith increasing severity of disease in an isolated women population from rural China, as is demonstrated by the increasing odds ratios from 1.68 for HPV positivity to 1.75 for persistent HPV and then 2.08 for CIN3+. Associated to these findings, it was showed that TB and cervical inflammation were diagnosed in 1% of the women, and associated with 90% higher odds of oncogenic HPV infection and 113% higher odds of persistent HPV infection. The authors of the “Shanxi Province Cervical Cancer Screening Study I” are considering that their results are consistent with the novel hypothesis that TB may provide an immunological profile that is associated with an increased susceptibility to HPV infection. In conjunction to this hypothesis, we can speculate like that MbTis associated to the loss/mutations in LKB1tumor suppressor, because persistence of small islands of squamous non-keratinizing cancer cells after radiation and chemotherapies.


5. Diagnosis

Regarding the diagnosis, one must consider the clinical presentation, physical examination, laboratory results, specially the microbiological ones and imagistic tools, and after the difficulties of the Romanian first published case of breast tubercular abscess on must reconsider an old concept of diagnosis—the “therapeutic” test.

5.1. Clinical presentation: physical examinations

5.1.1. Clinical presentation of breast TB

Clinical presentation of breast TB is variable regarding symptoms/signs: swelling of the breast 48.1% [65]; painless hard lump in approximately 60% cases [66], or pain is revealed as the first complain of some patients [67, 68] or up to 18.5% of cases [65]; rarely are recorded multiple lumps, the lump being with irregular borders, sometimes with skin fixation or to the underlying muscle or even chest wall, clinical findings imposing differential to breast carcinoma [69], situation which is much more suggested by the presence of an isolated breast mass, sometimes skin fixated “peau d’orange” sign, and without an associated sinus tract; abscess, unique or multiples; skin thickening; and skin sinus/fistula/multiple discharge sinuses [70], nipple retraction or inversion, nipple hyperpigmentation or focal discoloration –when the disease is long time duration [69], breast shape and sizes change, axillary lymphadenopathy (axillary lymph nodes are found in one-third of cases with breast TB [33]. Constitutional symptoms as fever, weight loss, night sweats or a failing of general health are infrequently encountered [71, 72].

5.1.2. Clinical diagnosis of cervix uteri tuberculosis

Irregular vaginal and postcoital bleeding with different aspects could occur at the cervix speculum examination such as exophytic-cauliflower aspect, tumoral-granulomatous, ulcerative and polypoid endocervical [73]. In many countries, even where tuberculosis is endemic, the majority of cases remain asymptomatic, but infected, and are discovered incidentally or remain undiscovered [22, 74]. Cervical examination of cases with cervical tuberculosis is normal in 90% cases, and the rest presents non-specific macroscopic changes, ulcerative/hypertrophic nodular lesions like proliferative cauliflower growth or fistulas/sinuses, or friable papillary growth covering almost the entire ectocervix. All these aspects may simulate invasive cervical cancer, or a miliary appearance [75, 76, 77]. There are reported cases with entire genital tract involvement, with myometrial alterations [78, 79], and association with tuberculosis of vulva and vagina [80].

5.2. Laboratory assessment

Current hematological and biochemical analysis are minimally influenced in cases with these MbTlocations. It is cited a high level of white blood cells, and of ESV [77].

5.2.1. Bacteriological diagnosis

The golden standard for TB diagnosis is to detect acid-fast bacilli (AFB) in the infected tissue, but it is well known how difficult is the Ziehl-Neelsen stain or the cultures for BK to become positive [67, 72, 81], because the necessity of a high number MbTin the smear (more than 10,000 bacilli/mL), and the slow growth of all mycobacterial species, including MbT,fact that partially explains the delay of TB diagnosis. It was recommended scanning with high-power oil immersion because these diagnosis difficulties, but the practice proved that scanning with a X 40 objective should suffice in most cases. There were proposed alternative stains to the conventional Ziehl-Neelsen stain, such as auramine/auramine-rhodamine using fluorescence technique [82], which in association to a higher power examination (x 600) may have better detection for MbT[83].

It is known that biopsy specimens that are cultured on Löwenstein-Jensen medium at room temperature yield pigmented mycobacterial colonies in 2–4 weeks. In the literature of bacteriology, it is very important the place for sampling, and leveling that may affect the sensitivity of a stain in the detection of rare organisms as Mycobacterium spp.or fungi. On the other side, for a better discovery for MbT, it is recommended to examine at least two blocks of biopsy instead of one [84]. In India, it is reported that are possible positive cultures of nipple discharge for Staphylococcus aureusassociated with positivity for MbT[85].

Actually many infections are detected by immunological assays proving the host competence, but for TB this aim is still a future desire; a very recently study of North American Universities’ Microbiology and Pathology Laboratories [86] have confirmed the limitations of serodiagnosis for active tuberculosis, including poor sensitivity and increased reactivity with non-tuberculous mycobacterium-positive patients. Bacteriological diagnosis of breast tuberculosis

The molecular diagnosis from clinical specimens is the aim of modern diagnosis of MbT,since many years, and this may be accomplished by nuclear acid amplification (NAA). The used methods allow the detection of mycobacterial DNA or RNA directly from the specimens, before the culture results are available [87]. Food and Drug Administration had accepted since the year 2000, two types of NAA, which were initially used for pulmonary tuberculosis, and later in extrapulmonary cases. The NAA is usually recommended when the smear evaluation is negative for AFB, and when clinical suspicion is very high, or when TB is endemic, but there are controversies on the specificity, sensitivity of the methods regarding the origin of specimen from respiratory tract or other sites [88]. The recommended tests are the enhanced MbTDirect Test (E-MTD; Gen-Probe, San Diego, CA) and Amplicor MbTTest (Amplicor; Roche Diagnostic Systems, Inc., Branchburg, NJ), and associated to these tests there were many studies about each value, specially for differential to granulomatous mastitis [12, 83, 89] or for the value of polymerase chain reaction (PCR) for real time MbTto compare to formalin-fixed, paraffin-embedded histologic specimens [90].

The real-time PCR for MbTon paraffin-embedded tissue is available with a high specificity of 99%, but low sensitivity of 65% for breast tissue in contrast to other types of specimens such as cerebral spinal fluid, urine and bronchoalveolar lavage, where sensitivity of more than 90% is reported, with comparable specificity [91, 92].

In the Romanian case, the molecular test—PCR for MbTon paraffin-embedded breast tissue was negative, and there are some researches [83, 93, 94] sustaining that molecular tests are not always relevant for the diagnosis of TB in smear-negative specimens. It is appreciated that real-time PCR for MbTis useful if positive, and confirms the presence of MbT, but if negative does not rule out the possibility of an infection [83]. Breast TB is paucibacillary and consequently tests such as microscopy, culture and NAA tests such as PCR techniques do not have the same diagnostic utility as they do in pulmonary tuberculosis [95]. There are some explanations for the negativity of the described tests for BK identification. One old explanation [84] is that the microorganisms have been killed and/or removed by the inflammatory process. Other explanation for PCR negativity is the existence of non-tuberculousinfections such as Corynebacteriumspp. [96], or non-tuberculous mycobacterium, which are now more common than tuberculosis in Western countries, and therefore would not be detected by this assay. Bacteriological diagnosis in cervical tuberculosis

The demonstration of the presence of MbTin the cervix uteri with the Ziehl-Neelsen staining was proved to be difficult in many reported cases all over the world, even in India and China [97]. In the Romanian case, MbTpresence in the endocervix was confirmed by PCR for MbTperformed on archived tissue (formalin-fixed paraffin-embedded uterine tissue).

5.3. Cytological diagnosis

5.3.1. Cytological diagnosis of breast tuberculosis

Actually fine needle aspiration cytology (FNAC) is considered a minimally invasive diagnosis method for breast pathology [98], including TB, because is revealing chronic granulomatous inflammation with caseating necrosis, presence of Langhans giant cell, and lymphocytic aggregates [99, 100, 101], but some studies are showing that in one quarter of cases FNAC is negative for breast tuberculosis diagnosis [71], because tissue samples collected at FNAC are not usually adequate for evaluation, or because caseating necrosis can be absent on the specimen. The absence of necrosis on breast specimen from FNAC does not exclude tuberculosis, which is sustained by other histological abnormalities [102]. In these situations, the next step for the diagnosis of mammary TB is the pathologic evaluation of specimens collected at open surgical biopsy [71], as it was done in the Romanian case, after the evaluation of the smear from fistula discharge.

5.3.2. Cytological diagnosis of cervix uteri tuberculosis

The Pap smear, a non-invasive procedure, may help in the diagnosis by the discover of epithelioid and multinucleated histiocytic cells, described since many years ago and rediscuss actually [103, 104, 105], fact that prompts further investigation. The epithelioid cells are elongated cells with pale eosinophilic cytoplasm, indistinct cell borders having large oval/elongated nuclei with a delicate chromatin pattern in singles/clusters. Multinucleated histiocytic cells, typical of Langhan’s cells type, have large number of delicate, often ovoid nuclei, some overlapping, arranged peripherally and often in horseshoe fashion. The presence of those multinucleated histiocytic giant cells may help to differentials to herpes virus infection—the cells have epithelial origin, but lower number of nuclei, and show characteristic crowding/molding without overlapping with eosinophilic inclusion in nuclei and cytoplasm, and also in post radiotherapy of postmenopausal women smears, where the cells have bad outline, and may contain some phagocytosed debris with radiation-induced changes [104]. In countries with endemic tuberculosis, it is appreciated that the Papanicolaou smear is helping very much the staff, the Ziehl-Neelsen stain of cervical smear, and fluorescent technique and culture are confirming later [105]. The Romanian woman was not postmenopausal, a viral infection with high-risk HPV was clearly demonstrated, by genotyping of the cervix after surgery, but these type of cells were absent in the smear.

5.4. Pathological diagnosis of MbTinfection

5.4.1. Pathological diagnosis in breast MbTinfection

There are known two pathological classifications of breast tuberculosis: an old one—McKeown and Wilkinson [106] cited by Bahoroon [107], and a recent one—Tewari and Shukla [7].

McKeown and Wilkinson [106] had classified breast tuberculosis into five pathological varieties: (1) nodular—the most common variety presenting as a localized mass, with extensive caseation, and little fibrosis; (2) diffuse or disseminated—second most common variety, involving the entire breast with multiple intercommunicating foci of tubercles within the breast, which caseate leading to ulceration and discharging sinuses; (3) sclerosing—extensive fibrosis rather than caseation is present, suppuration is rare, the entire breast is hard, the nipple is retracted/inverted, category which is often mistaken for breast carcinoma; (4) tuberculous mastitis obliterans, characterized by duct infection producing proliferation of the lining epithelium, and marked epithelial and periductal fibrosis; and occlusion of the ducts, with appearance of cystic spaces, and all these resemble “cystic mastitis” and (5) acute miliary tuberculous mastitis, which occurs as a part of generalized miliary tuberculosis. The last two entities have only historical importance, being rarely described in the recent medical literature.

The Indian pathologists [108] have introduced a new pathological classification of breast tuberculosis, with three categories: (1) nodulo-caseous tubercular mastitis; (2) disseminated/confluent tubercular mastitis and (3) tubercular breast abscess.

There are some controversial discussions about the “granulomatous mastitis”, diagnosed during childbearing period, usually in parous women, in early 1930s, which are frequently misdiagnosed as tuberculosis or carcinoma [108], with negative culture for MbT, and with cytological and immunocytochemical findings definitely for differential diagnosis from breast tuberculosis at fine needle aspiration cytology [109] or at open surgery. The pathological changes induced by MbTin breast make the differences to other breast pathology, “idiopathic granulomatous mastitis”, which is also a “masquerader” [25, 28]. Tuberculous mastitis is often considered a form of “granulomatous mastitis” secondary to breast MbTinfection, and some authors reserve the term of “granulomatous mastitis” to “idiopathic granulomatous mastitis”, a chronic breast inflammatory entity [110]. Granuloma is a defense mechanism against antigens, which stay in many organs without inactivation. The granulomatous lesions are classified into infectious, vasculitis, immunological, chemicals and neoplasia [35], or the recent classification is more simple: infectious and non-infectious granulomas, with the prove from new studies that pathogenic microorganism are suspected to be a cause of granuloma in non-inflammatory diseases [111].

The etiology of “granulomatous mastitis” is unclear, being postulated, and sometimes proved, the autoimmune factors [112], sarcoidosis, fat necrosis, undetected organisms (as blastomycosis, actinomycosis, cryptococcosis, histoplasmosis, filarial infection and corynebacterium), Wegener’s granulomatosis, reaction to childbirth, and use of oral contraceptives, ductular ectasis [113] the last two factors are present in the reported case. “Granulomatous mastitis” was the first diagnosis in authors’ mind at the beginning of investigations, and this is partially an explanation of the delay in diagnosis, and late specific antitubercular treatment, as in other cases from literature in the last years [12]. These breast pathologies – tuberculosis and “idiopathic” granulomatous mastitis are considered “masquerader” [28] or “imitator” [89].

There are described some pathological characteristics [107, 114, 115], which make the differentiation between the “idiopathic “granulomatous mastitis”—first described by Kessler and Wolloc [113], and breast TB. TB is affecting all breast structures (lobules, ducts, fat; some pathologists consider that ducts are specially affected), and the tubercular granulomas are associated to caseating necrosis which makes the name of “caseating granulomas”, and the difference from “idiopathic “granulomatous mastitis [107, 116], which was named “lobular non caseous granuloma” (Table 2). The isolation of MbTin the central necrosis increases the sensitivity of the diagnosis.

Characteristic“Idiopathic” granulomatous mastitisTubercular mastitis
Macroscopic characteristic
Isolated or multiple breast massesCommonCommon
Multiple sinuses or fistulasAbsentPresent
Focal discoloration of areolaAbsentPresent
Microscopic characteristic
Structure affectedMammary lobules from one breast, rarely bilateralAll mammary structures: ducts, lobules, fat, commonly bilateral
Type of lesionGranulomas of the lobulesGranulomas of all mammary structures
Histological components of breast’s granulomasEpithelioid histiocytes, Langhans giant cells, lymphocytes, plasma cells, and occasionally eosinophilsEpithelioid histiocytes, Langhans giant cells, lymphocytes, rare plasma cells, and eosinophils
Foamy cellsAbsentPresent
Caseating necrosisAbsentPresent
Fat necrosisPresentPresent

Table 2.

Macroscopic and microscopic characteristics of “idiopathic” granulomatous mastitis and tubercular mastitis (modified from Akcan et al. [114]; Baslaim et al. [115]; Bahoroon [107]; Lacambra et al. [109]).

There are mentioned some other types of “necrositing granulomas” in which infections-inflammation are frequently associated, and are proved with special stains (as Ziehl-Neelsen or Grocott Methamine Silver), and/or by cultures, and other granulomas with infection-inflammatory aspect, but without associated infections as eosinophylic necrosis or basophilic necrosis [83], as is Wegener’s granulomatosis, and less commonly rheumatoid nodule, necrotizing sarcoid granulomatosis, infarct and lymphomatoid granulomatosis [83]. The granulomas with eosinophilic necrosis have regular rounded contour, the rim being formed of epithelioid histiocytes with multinucleated giant cells, and the center may have coagulative type of necrosis, which is like an infarct. The Wegener’s granulomatosis is characterized by ‘dirty’ basophilic necrosis with irregular geographic necrosis; the necrosis is rimmed by palisading histiocytes and scattered multinucleated giant cells, with hyperchromatic nuclei and peripheral to the necrosis is the necrotizing vasculitis in vessels. The vessels display transmural fibrinoid necrosis, and the necrosis of the media with admixed necrotic neutrophils, which contributes to the diagnosis with true necrotizing vasculitis. The granuloma of the Romanian case has multiple normal vessels. The parenchymal necrosis of the necrotizing sarcoid granulomatosis is variable, usually eosinophilic but can be irregular and basophilic, mimicking Wegener’s granulomatosis.

The pathological characteristics of the “idiopathic” lobular non-caseating granulomas and of tuberculosis caseating granuloma of the breast are listed in Table 2, and it is considered [83] that no single histological feature may distinguish infectious necrotizing granulomas from other specific disorder as Wegener’s granulomatosis or sarcoidosis, being necessary a combination of multiple pathological features to establish the specific diagnosis.

The first reported case of this chapter is a primary breast TB, with no personal history, or other focus on the systemic physical/radiological examinations for TB. The diagnosis of breast TB must follow the general principles: clinical and laboratory. The clinical presentation of breast TB is variable regarding symptoms/signs: swelling of the breast—48.1% [10]; painless hard lump—approximately 60% cases, or pain is revealed as the first complain of some patients [67, 68] or up to 18.5% of cases [10]; rarely are recorded multiple lumps, with irregular borders, sometimes with skin fixation or areola fixation, or to the underlying muscle or even chest wall, clinical findings imposing differential to breast carcinoma [69], situation which is much more suggested by the presence of an isolated breast mass, sometimes skin fixated-“peau d’orange” sign, and without an associated sinus tract; ulceration of areola [117], or of the skin covering the mammary gland [118]; abscess, unique or multiples [85]; skin thickening and skin sinus/fistula/multiple discharge sinuses [70], nipple retraction or inversion, nipple hyperpigmentation or focal discoloration—when the disease is long time duration [69], or distruction of nipple-areola region [19], breast shape and sizes are changed, axillary lymphadenopathy (axillary lymph nodes are found in one-third of cases with breast TB). Constitutional symptoms as fever, weight loss, night sweats or a failing of general health are infrequently encountered [71, 72].

5.4.2. Pathological diagnosis of cervical tuberculosis

The cervical tuberculosis diagnosis is commonly established by the Papanicolaou smear without any dysplasia, positivity for acid-fast bacilli, and the cervical biopsy (punch, loop excision biopsy) showing granulomatous inflammation with caseous necrosis, facts that were absent in the Romanian case. The presence of the viral infection is clearly proved by genotyping of the cervix after surgery. The endocervical curettage which has the possibility to diagnose associated endocervical tuberculosis was not done, because they believe that exocervical lesion was the only cause of abnormal bleeding. The pulmonary tuberculosis was 7 years previously registered, and the genital location was diagnosed in the endocervical glands, on the specimen collected at hysterectomy—after radiotherapy and chemotherapy. The presence of the endocervical tubercle bacillus was indirectly diagnosed by the pathologic examination the presence of caseous necrosis and Langhans multinuclear giant cells, and by PCR for MbT. The diagnosis of TB depends also upon the isolation of the MbTon microscopy, and culture, and by the PCR. Culture of MbTand acid-fast staining was not done, the cervical granulomas were noted at pathological examination after surgery, on a formalin-fixed specimen. The presence of characteristic, typical caseous granuloma was appreciated sufficient to make the diagnosis [77, 119], but many researchers consider that it is very important to distinguish between the granulomatous reaction and tuberculosis by more specific methods [120]. The presence of stroma caseous necrosis was sufficient for the positive diagnosis of cervical TB in the Romanian authors’ opinion. The granuloma diagnosis is a microscopic diagnosis. The microscopy of the cervical specimen after radical hysterectomy reveals an aggregate of immune cells, appearing as epithelioid macrophages, and if a foreign body or a parasite is not observed inside the granuloma, stains for acid-fast bacilli, and fungi are ordered as mycobacteria and fungi (such as Cryptococcus, Blastomyces, Coccidioidesand Aspergilluscan be seen on hematoxyline-eosine, preferentially in the area of necrosis rather than the surrounding viable area) are frequently the cause of this type of inflammation [31]. In cases with samples fixed in formalin the detection of the infectious agent is recommended to be done by molecular analysis, PCR for MbTin the Romanian case [91, 118].

5.5. Imaging diagnosis of rare tuberculosis locations

5.5.1. Radiological imaging of breast tuberculosis

Radiological imaging of breast tuberculosis is appreciated not to be diagnostic, and the described mammographic images are in connection to three patterns of breast tuberculosis: nodular, disseminated and sclerosing patterns [121]. Some radiological characteristics are common for all patterns, like the change in shape, and outline of the breast mass—seen in the standard views, the reduction in size of the affected breast, skin thickening, nipple retraction and ill-defined breast mass [122]. In previous radiological studies, the skin bulge and sinus tract sign, which connects the breast density to a localized skin thickening or to the skin bulge are the radiological features strongly suggestive for tubercular breast abscess [66].

In the Romanian case, the mammography was not recommended, because authors thinking was dominated by a chronic inflammation with repeated episodes of recurrence, as a granulomatous mastitis or a plasma cell mastitis.

Some clinicians [123] recommend computed tomography scan, when are doubtful cases, for the differentiation of primary and secondary lesions, to evaluate accompanying pulmonary disease, if it is present or to detect the continuity of the breast lesions with the thoracic wall or pleura, and associated lesions of the lungs.

5.5.2. Ultrasonography for breast tuberculosis

In the literature, there are controversies about the value of ultrasonography for breast TB diagnosis. On one side, it is mentioned no specificity of the ultrasound examination [121]: the breasts’ lesions may appear as heterogeneous, hypoechoic, irregularly or ill-bordered masses of different sizes, but usually small sizes, with internal echoes or thick-walled cystic lesions, some mass may present posterior acoustic enhancement, in association to the fistula formation, and the thickening of Cooper’s ligaments and subcutaneous tissues, as it was revealed in the Romanian case. On the other side, it is mentioned an unique finding strongly suggestive for breast TB: the presence of a dense sinus tract connecting an ill-defined breast mass to localized skin thickening and bulge [14].

Regarding the vascularisation of the breast tubercular masses, the blood flow was not observed within the lesions, while increased circumferential vascularization was seen in the color Doppler ultrasound, and the spectral evaluation shows a low resistance monophasic flow pattern [121].

5.5.3. Magnetic resonance imaging (MRI) for breast/cervix uteri tuberculosis diagnosis

If on recommend MRI imaging for breast TB, it is possible to detect parenchymal asymmetry with enhancement, micro-abscesses, and peripherally enhanced masses. MRI may reveal lymphadenopathy along the pelvic walls, with an abnormal signal to the entire body of the uterus and sometimes when the entire uterus is infected by MbT, the endometrial cavity, myometrium, and junctional zone could not be differentiated and thus the radiological appearance was consistent with Asherman’s syndrome [77].

5.6. Antitubercular therapeutic test for rare location tuberculosis diagnosis

There are cases with pulmonary and extrapulmonary TB with negative molecular test—PCR for MbTfrom clinical specimens or it is not possible to recommend and use the rapid very efficient modern molecular NAA for detection of mycobacterial DNA or RNA directly from the specimens as it was previously discussed. In countries with endemic TB, it is since long time discussed and recently it is recalled an empirical antitubercular therapy even in the absence of positive acid-fast bacilli, and without culture—positive results, or when it is the suspicion of TB or when the “idiopathic” granulomatous mastitis is found and it is not responding to metothrexate or corticosteroids [108, 117].

TB is considered to be actually under-diagnosed in Romania, and the Romanian health history had a similar management in cases which are mentioned before, and in these conditions, the final diagnosis of the case with primary recurrent non-gestational breast abscess was done after the antitibercular” therapeutic” test, which was efficient after the first two months. More details are in the subsection 8 on “Treatment”.


6. Differential diagnosis

6.1. Differentials for breast tuberculosis

The breast tuberculosis can be confused with breast carcinoma, specially in elder women [27, 28, 69, 124], who present an isolated ill defined, irregular, occasionally hard breast lump without sinuses/fistula, but pain is present more frequently in the tuberculous lump than in carcinoma. Involvement of the nipple and areola is rare in tuberculosis, but fixation of the lump to the skin may be present as a part of the inflammatory process, which is present in both pathological entities A high index of suspicion needs to be maintained if a breast lump is associated with a sinus or indolent lump in an immigrant women if this is encountered in the western countries. The coexistence of tubercular axillary lymphadenitis with breast carcinoma can falsely over-stage the disease [125], and is reported an association of the metastasis of breast carcinoma and axillary tuberculous lymphadenitis [126]. In postmenopausal women is considered that the diagnosis of breast TB does not exclude a concomitent cancer [3], situation that was first reported by Pilliet and Piatot in (cited by [27]).

In cases with discharging sinuses associated to a breast lump it is necessary to make the differentiation from actinomycosis by the absence of sulfur granules in the discharge and by fungal culture [9].

For women from countries with endemic tuberculosis from Asia and Africa, or immigrated from that countries, the association of breast carcinoma and tuberculosis must be thought, specially when the data are confusing [3, 127, 128], as it is when on records tuberculosis of axillary lymph nodes with primary breast cancer [129], or axillary lymph nodes with granulomas and a breast carcinoma [72, 130].

Beside carcinoma there are other misdiagnosis risks as “idiopathic” granulomatous mastitis (Table 2, for pathological differential), or plasma cell mastitis (which may mimic histological the tuberculosis by the presence of foreign body giant cells, epithelioid cells which are arranged in tubercles, besides plasma cells, polymorphs, lymphocytes and few foamy macrophages, but is missing the caseation which makes the differential from tuberculosis- [131], lupus mastitis [132], eritema nodosus [133].

In the last years there are described recurrent breast abscess to be more frequent due to non-tuberculous mycobacterial infection [20, 134], cases with similar clinical presentation, with granulomas.

6.2. Differentials for cervix uteri tuberculosis

When women’s complaints are present, and cervical examination shows cervical changes it is considered to think about both pathologies, separately or associated in countries with high risks for these pathologies. There are discussed other viral cervical infections as HIV, herpes virus simplex, other sexual transmitted (Treponema pallidum, Trichomonas vaginalis, Neisseria gonorrhea) or parasitic diseases as schistosomal, amoebic, brucella, tularaemia which may induce chronic cervical granulomas, sarcoidosis, and foreign body reaction [77], or more rare an epithelioid granulomas in Hodgkin’s disease [39].


7. Complications of breast/cervix uteri tuberculosis

When not adequate treated, TB mastitis is followed by abscesses, which can penetrate the retromammary space [135], or to the ribs [136], formation of sinuses, and nipple retraction, and irreversible inversion, recurrences even with surgical drainage/excision, and breast mutilation [26].

In the case with the association of two severe immunosuppressive diseases as tuberculosis and cancer there are risks for reactivating the lung tuberculosis, for lung metastases from cervical cancer, and of high mortality in patients with coexistent disease [137, 138].


8. Treatment of breast/cervix uteri tuberculosis

Treatment may cure the disease with antitubercular drugs, and surgery is rarely required, being used in cases resistant to medical treatment. The specific antitubercular treatment was delayed in the Romanian case with breast abscess as is frequently mentioned in literature [24], because the difficulties of the positive and differential diagnosis, and because tuberculosis is under-diagnosis in contemporary Romania, but the attitude regarding tuberculosis was similar in the Romanian health history to that from tuberculosis endemic countries: to recommend empirical antitubercular therapy even in the absence of positive AFB, and without positive culture results, when it is a suspicion of TB or when the granuloma is found. In many cases, the decision for the antitubercular treatment is taken after the failure of corticoids and methotrexate therapy for “idiopathic” granulomatous mastitis [108, 117, 139].

Based on patient profile, clinical features and lack of response to usual antibiotic therapy, it is recommended a four-drug (isoniazid, rifampin, ethambutol and pyrazinamide) 6-month course of Directly Observed Therapy Short-Term (DOTS) - Category I [117], but the response to treatment is variable and not dramatic. There are reported excellent results with such management [101].

There are no specific available guidelines for chemotherapy of breast TB, and the therapy generally follows guidelines that are used for pulmonary TB. The regimen consists of a 2 month intensive phase (isoniazid, rifampicin, pyrazinamide and ethambutol), followed by a 4 month continuation phase (isoniazid and rifampin). It is recommended another regimen with extension of continuation therapy for a longer period to 7 months [9, 140, 141, 142] or more up to 12–18 months [140], because the wish to lower the relapse rate. There is also a regimen which combines first and second lines antitubercular drugs, including kanamycin, ofloxacin, ethionamide, para-amino salicylic acid (PAS), pyrazinamide and isoniazid, with the reason of the risk of multidrug resistant strains [143]. The breast lesions and tenderness are steadily improved after 2 months of intensive therapy the breast lesions and tenderness are steadily improved [83] (Table 3).

Treatment durationInitial phase treatment (intensive therapy)Continuation treatment
6 months*2 months of:
300 mg isoniazid,
600 mg rifampin,
1500 mg pyrazinamide,
1000 mg ethambutol or
streptomycin 1 g per day
4 months of isoniazid, rifampin
9 months**2 months of:
300 mg isoniazid,
600 mg rifampin,
1500 mg pyrazinamide,
1000 mg ethambutol
per day
7 months of isoniazid, rifampin

Table 3.

Breast antitubercular regimens.

Al-Marri et al. [122]; Jalali et al. [102]; Mirsaeidi et al. [6], Bahoroon [107]; Gon et al. [28]; Singal, et al. [13].

Daali et al. [141]; Khanna et al. [9]; Kumar et al. [143].

In the Romanian primary recurrent non-gestational breast abscess was recalled as the old concept of the “antitubercular therapeutic” test, for the final diagnosis and it was proved to be efficient after the first 2 months, and the association of isoniazid and rifampin was continued with excellent results up to 9 months.

Surgery was imposed in the Romanian case because of abscess complications in the conditions of MbTlate diagnosis. It was a minimal surgical intervention required for drainage and excision biopsy of abscesses’ wall. Surgery is commonly reserved for selected cases, in particular situations, and in different manner:

  • According to the presence of breast masses/lump and abscesses with fistula: simple or segmental mastectomy or quadrantectomy or drainage of abscess with large excision of the necrotic tissue of the breast and excision of the axillary lymph nodes when involved [25].

  • Breast abscesses with negative bacteriological tests in order to diagnose by excision biopsy of the abscess wall and drainage of abscess with fistula [16, 21, 67].

  • In cases refractory to medication [69].

  • Residual lumps after antitubercular therapy, excision of sinus [9, 10].

  • Mastectomy when is severe breast destruction [14].

A special mention is for the percutaneous treatment with drainage controlled by CT and specific antibiotic antitubercular drugs [123], especially when resistance to ATT is discovered [144], as it is done for pulmonary TB and for abdominal collections [145].

The ATT are usually recommended for cervix uteri tuberculosis for minimum 6 months [146], healing being proved by repeated biopsy. The chemo and radiotherapy, and the radical surgical intervention done in the Romanian case were imposed by the initial diagnosis of squamous non-keratinized cervical carcinoma stage IB, tubercular cervicitis being a postoperative surprise, and it was decided to avoid a new cure of AAT because the postoperative assessments for MbTlung or general reactivation were negative.


9. Conclusions

  • Breast tuberculosis should be considered as a differential diagnosis of breast inflammatory disease or masses, all over the world, not only where tuberculosis is endemic.

  • Tuberculosis must be suspected in recurrent breast inflammatory disease with negative current cultures, and negative tests as Ziehl-Neelsen stain, culture and PCR for MbT.

  • The pathologic examination of the open biopsy in the reported case is suggesting the diagnosis of a granulomatous mastitis, and the multinuclear giant cells of Langhans type presence ensure the diagnosis of tubercular granulomatous mastitis even in the absence of the characteristic caseous necrosis.

  • The final diagnosis of breast TB was established by specific antitubercular drugs, which represents a Tuberculosis Diagnosis Test, and may avoid or delay breast characteristic mutilations when treatment is not adequate.

  • The cervix uteri tuberculosis presence and its association to ecto/endocervical cancer is to be suspected not only in developing countries with endemic tuberculosis and high rates of HPV/HIV infections, in patients with primary lung/other organs tuberculosis.

© 2018 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms of the Creative Commons Attribution 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to cite and reference

Link to this chapter Copy to clipboard

Cite this chapter Copy to clipboard

Manuela Cristina Russu, Şerban Nastasia, Daniela Degeratu and Ruxandra Viorica Stănculescu (September 26th 2018). Breast and Cervix Uteri: Rare Locations for Mycobacterium Tuberculosis Infections and Complications-Cases Report and Literature Review, Tuberculosis, Jean-Marie Ntumba Kayembe, IntechOpen, DOI: 10.5772/intechopen.75044. Available from:

chapter statistics

730total chapter downloads

More statistics for editors and authors

Login to your personal dashboard for more detailed statistics on your publications.

Access personal reporting

Related Content

This Book

Next chapter

Urinary Tract Tuberculosis

By Gerardo Amaya-Tapia and Guadalupe Aguirre-Avalos

Related Book

First chapter

Angiogenesis and Lung Cancer

By S. Vázquez, U. Anido, M. Lázaro, L. Santomé, J. Afonso, O. Fernández, A. Martínez de Alegría and L. A. Aparicio

We are IntechOpen, the world's leading publisher of Open Access books. Built by scientists, for scientists. Our readership spans scientists, professors, researchers, librarians, and students, as well as business professionals. We share our knowledge and peer-reveiwed research papers with libraries, scientific and engineering societies, and also work with corporate R&D departments and government entities.

More About Us