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Medicine » Surgery » "A Textbook of Advanced Oral and Maxillofacial Surgery Volume 2", book edited by Mohammad Hosein Kalantar Motamedi, ISBN 978-953-51-2035-3, Published: April 22, 2015 under CC BY 3.0 license. © The Author(s).

Chapter 16

Considerations for the Spread of Odontogenic Infections — Diagnosis and Treatment

By Flaviana Soares Rocha, Jonas Dantas Batista, Cláudia Jordão Silva, Roberto Bernardino Júnior and Luis Henrique Araújo Raposo
DOI: 10.5772/59161

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Anatomy of the fascial spaces in axial (A) and coronal (B) images. SMS: submandibular space; SLS: sublingual space; PPS: parapharyngeal space; CS: carotid space; MS: masticatory space. SMG: submandibular gland; GGM: genioglossus muscle; MHM: mylohyoid muscle; MM: masseter muscle; MPM: medial pterygoid muscle; LPM: lateral pterygoid muscle; TM: temporal muscle.
Figure 1. Anatomy of the fascial spaces in axial (A) and coronal (B) images. SMS: submandibular space; SLS: sublingual space; PPS: parapharyngeal space; CS: carotid space; MS: masticatory space. SMG: submandibular gland; GGM: genioglossus muscle; MHM: mylohyoid muscle; MM: masseter muscle; MPM: medial pterygoid muscle; LPM: lateral pterygoid muscle; TM: temporal muscle.
Different locations of odontogenic infections. (A) Submandibular and sublingual region. (B) Submandibular region. (C) Cervical region. (D) Palate. (E) Orbital region. (F) Submandibular and buccal region.
Figure 2. Different locations of odontogenic infections. (A) Submandibular and sublingual region. (B) Submandibular region. (C) Cervical region. (D) Palate. (E) Orbital region. (F) Submandibular and buccal region.
Clinical (A) and radiographic(B) aspects of a periapical lesion.
Figure 3. Clinical (A) and radiographic(B) aspects of a periapical lesion.
Clinical presentation of Ludwig’s angina.
Figure 4. Clinical presentation of Ludwig’s angina.
Sequence of drainage of odontogenic infection – case 1. Note that the most dependent part (under the swelling) must be incised not the thin most swollen part (to prevent scarring).
Figure 5. Sequence of drainage of odontogenic infection – case 1. Note that the most dependent part (under the swelling) must be incised not the thin most swollen part (to prevent scarring).
Figure 6: Sequence of drainage of odontogenic infection – case 2.
Figure 6. Figure 6: Sequence of drainage of odontogenic infection – case 2.

Considerations for the Spread of Odontogenic Infections — Diagnosis and Treatment

Flaviana Soares Rocha1, Jonas Dantas Batista1, Cláudia Jordão Silva1, Roberto Bernardino Júnior2 and Luis Henrique Araújo Raposo3

1. Introduction

The goal of this chapter is to present the basis for correct diagnosis and management of severe odontogenic infections. The knowledge of the anatomy of fascial spaces is essential for the correct diagnosis and treatment of head and neck infections, because both facial and cervical fasciae work as an effective barrier against the spread of infections in this region[1, 2]. Once these infections occur, they are often difficult to assess accurately by clinical examinations and conventional radiographic techniques, and the outcome may be serious and potentially life-threatening[3]

The fasciae of the neck are glossy and divided into two separated layers: the superficial fascia and the deep fascia. The superficial fascia is actually a component of the fatty subcutaneous tissue while the deep cervical fascia is divided into three layers: the superficial layer, the visceral or middle layer, and the pre vertebral or deep layer. The deep cervical fascia plays an important role in determining the location and course of spread of infections within the soft tissues of the neck. The infections that commonly affect head and cervical areas are frequently from odontogenic origin and to a lesser frequency, proceeding from foreign bodies or trauma to this region[4]. An impacted mandibular third molar is one of the most frequent causes of odontogenic infection[5-7]. Moreover, an semi-impacted third molar results in odontogenic infection more commonly than fully erupted or completely impacted molars [7].

Odontogenic infections occasionally spread beyond the barriers of the fascial spaces, which are formed, as seen, by the deep cervical fascia of the suprahyoid regions of the neck[2]. Among various spaces, the submandibular space is one of the first to be involved in odontogenic infections, similar to the masticatory space[2]. As infection may spread along deep cervical facial planes and neck cavities, widespread cellulitis, necrosis, abscess formation, and sepsis may occur in these cases[4]. Therefore, it is important to understand the anatomy, rate of progression and potential for airway compromise of an infection[7].Spontaneous dissemination of an odontogenic infection is however, very rare in immunocompetent patients[8, 9]. In patients with anatomical abnormalities, systemic diseases or immunosuppression, bacteremia caused by dental procedures may lead to generalized or metastatic systemic infection complications leading to hospital care[10, 11]. In particular, patients with poorly controlled diabetes mellitus are more susceptible to bacterial infections[12-14]. However, death from odontogenic infection is quite rare [9, 15, 16].

Despite being rare, facial and neck fasciae spaces involved by infections from odontogenic origin may lead to a very morbid condition. The diagnosis delay and late or wrong therapeutic approachs to deep infections in these areas are the main causes of high mortality rate in this life-threatening situation.[4] Dentistry has made great progress in prevention and early intervention of odontogenic infection. The introduction of antibiotics reduced significantly the mortality and morbidity of these infections, however, even in this contemporary postantibiotic era, serious infections such as a descending necrotizing mediastinitis still have a high mortality rate with a fulminating course, leading frequently to death.[17-20]

2. Facial and cervical space anatomy

The knowledge of the relevant facial and cervical anatomy of the face is essential for todays clinical practice, allowing precise and successful diagnosis. Figure 1 describes the principal anatomic structures and spaces of the face.


Figure 1.

Anatomy of the fascial spaces in axial (A) and coronal (B) images. SMS: submandibular space; SLS: sublingual space; PPS: parapharyngeal space; CS: carotid space; MS: masticatory space. SMG: submandibular gland; GGM: genioglossus muscle; MHM: mylohyoid muscle; MM: masseter muscle; MPM: medial pterygoid muscle; LPM: lateral pterygoid muscle; TM: temporal muscle.

The superficial fascia a component of the fatty subcutaneous tissue and the deep cervical fascia is an important anatomic structure, determining the location and course of spread within the soft tissues of the neck.

2.1. Deep cervical fascia

The deep cervical fascia is divided into three layers: the superficial layer, the visceral or middle layer, and the pre-vertebral or deep layer.

The superficial layer of the deep cervical fascia encircles the neck, enveloping the sternocleidomastoid and trapezius muscles and the muscles of mastication, along with the submandibular and parotid salivary glands. It extends from the nuchal line of the skull, mastoid processes, and mandible inferiorly to the scapula, clavicle, and lower cervical vertebrae.

The middle layer of the deep cervical fascia encloses the anterior viscera of the neck (thyroid gland, larynx, trachea, and pharynx) and the strap muscles. It attaches to the skull base and extends into the mediastinum.

The deep layer of the deep cervical fascia is divided into the pre-vertebral and alar divisions. The pre-vertebral division tightly encloses the spine and paraspinous muscles. Ventrally, it lies immediately anterior to the vertebral bodies, forming the anterior wall of the pre-vertebral space. It extends from the base of the skull to the coccyx.

The alar division of the deep layer of the deep cervical fascia lies between the pre-vertebral division and the middle layer of the deep cervical fascia. It extends from the skull base to the mediastinum. The carotid sheath is made of contributions from all three layers of the deep cervical fascia and envelops the carotid artery, jugular vein, and vagus nerve.[21, 22]

2.2. Fascialspaces

The parapharyngeal space fascia is in an area of fatty areolar tissue with complex fascial margins that lies in a central location in the deep face. It extends from the skull base to the hyoid bone, containing only fat tissue, branches of the trigeminal nerve, and the pterygoid venous plexus. Posterior to the parapharyngeal space is the carotid space. All three layers of deep cervical fascia contribute to the carotid sheath that circumscribe this space.

The carotid space extends from the skull base to the aortic arch. Its suprahyoid contents include the internal carotid artery, jugular vein, cranial nerves IX–XII, and deep cervical lymph node chain.

The retropharyngeal space is a posterior midline space that has the middle layer of deep cervical fascia as its anterior margin and the deep layer of deep cervical fascia as its posterior and lateral margins. It extends from the skull base to the level of the T3 vertebral body.[21, 23]

The danger space lies posterior to the retropharyngeal space and is separated from the retropharyngeal space by the alar fascia. The posterior margin of the danger space is the pre-vertebral division of the deep layer of the deep cervical fascia. The importance of the danger space, and the reason for its name, is that it extends from the skull base to the level of the diaphragm, providing a pathway into the posterior mediastinum and pleural spaces. Infections of danger space most commonly occurs when an abscess in the retropharyngeal space ruptures through the alar fascia.[21, 23-31]

3. Teeth involved in fascial infections

Invasive dental manipulation is known to cause bacteremia and generally considered high-risk procedures for the spread of infection in susceptible patients.[31-48] Sato et al., has shown that the main origin of maxillofacial infections were odontogenic (79.31%), followed by trauma (10.7%), immunosuppression (1.6%), pathologies (1.6%), and other causes (8%).[49] Seppänen et al., also reiterated that the most common dental procedures that precede odontogenic infection complications are: tooth extraction (60%), endodontic treatment (20%), dental implant surgery (8%), restorative treatment (8%) and dental plaque and calculus removal (4%).[50-52]

Lower third molars are more frequently involved in odontogenic infections when compared with other teeth. Flynn et al., presented in their prospective study with 37 consecutive hospitalized patients, a 68% prevalence rate of this group of teeth in association with odontogenic infections, followed by other lower posterior teeth (premolars, first and second molars), without anterior teeth involvement.[13] Third molar removal is one of the most regular dentoalveolar surgical procedures.[10, 26, 52-65] With an 80% prevalence of retained third molars in the adult population,[23] appropriate treatment, and especially prophylactic third molar removal remains a key focus of interest in healthcare with both medical and economic dimensions. It is generally accepted that substantial risks may arise both from third molar removal,[6, 29, 37, 60, 66, 67] as well as from a “wait and see “policy.[4, 11, 14, 25, 33, 44, 65]

4. Microbiological involvement

The severe infections of odontogenic origin frequently involve a complex polymicrobial mix of aerobes, facultative aerobes and strict anaerobes working together. Some species like Peptostreptococcus, Staphylococcus, Lactobacillus, Prevotella, Treponema, Fusobacterium, Veillonella, Actinomyces, Bacteroide ssp. and oral Streptococcus sp. are frequently associated with infections of odontogenic origin.[13, 36, 43, 46, 48, 56] Sakamoto et al., reported 17 different species collected from a single surgical site.[48] Flynn et al., isolated 90 different strains of microorganisms in 37 patients, and of these, 17 were penicillin-resistant.[13] Other species can be easily found at the infection sites, but generally, they reflect the indigenous microflora of the oral cavity. Routine culture and sensitivity testing for minor oral infections does not appear to be justified, however, when an infection involves anatomic spaces of moderate or greater severity, or when there is significant medical/immune compromise, the tests become important to the outcome.

5. Pathway of facial and cervical infections of odontogenic origins

5.1. Fascial infections derived from mandibular odontogenic origins

Infections originating in the facial planes of the head and neck spread downward along the cervical fascia, facilitated by gravity, breathing, and negative intrathoracic pressure. Knowledge of the facial spaces and fascial planes is essential for understanding the propagation, pathways, symptoms, and complications of cervical infections.[4, 47] Although the pattern of spread varies among patients, a relatively constant trend in the distribution of infection into the spaces seem to be evident. Some studies clearly demonstrated that the masticatory space is the most prevalent site for odontogenic infection spread. Taken together with the finding that the masticatory space encompasses the posterior mandibular body, ramus, and a part of the alveolar bones of the maxilla, this suggests that the masticatory space may be the initial site of spread of odontogenic infection. This contention was further supported by the finding that mandibular infection more frequently involved the masseter and medial pterygoid muscles (located in the lower compartment of the masticatory space where the mandible is included) than the temporalis and lateral pterygoid muscles (located in the upper compartment of the space where part of the maxilla is included).[3]

The spaces adjacent to the masticatory space are the parotid space posteriorly, the parapharyngeal space medially, and the submandibular and sublingual spaces inferiorly (Figure 1).[48] The parapharyngeal space occupies the central position among the masticatory, parotid, and carotid vascular spaces. Therefore, infections in the parapharyngeal space may originate from any adjacent space. A fascia extends from the posterior superior margin of the medial pterygoid muscle to the base of the skull to separate the masticatory space from the parapharyngeal space.[49] In this way, it is possible to believe that infection spreading from the masticatory space into the parapharyngeal space may pass via the medial pterygoid muscle. Yonetsu et al., found that 100% of patients with parapharyngeal space involvement also had the medial pterygoid muscle affected, and 79% of patients with infection in the medial pterygoid muscle area had concomitant involvement of the parapharyngeal space. However, in none of their cases spread from the submandibular into the pharyngeal spaces.[3]

The parotid space abuts the posterior masticatory space and is enveloped by a layer of the deep cervical fascia.[50] Yonetsu et al., demonstrated that odontogenic infection may extend into the parotid space, via the masticatory space.[3] The retropharyngeal space connects the skull base to the upper mediastinum and contains loose fatty tissue in its infrahyoid portion. Thus, the retropharyngeal space is considered to be important due to its proximity to the airway and because infections in this space may cause mediastinitis, bronchial erosion, and septicemia.[3, 50] The vertebral and vascular spaces are thought to be rarely involved by head and neck infection.[51]

The infection spread occurs when accumulated pus perforates bone at the weakest and thinnest part. In the mandible, the lingual aspect of the molar region represents the easiest way.[4, 52] If odontogenic infection perforates this portion of bone, it will spread into the sublingual or submandibular space. As these spaces are partially separated by a thin sheet of mylohyoid muscle, infection in either space easily spreads into the other. It is generally believed that the midline enables free communication from either the sublingual or submandibular space.[3, 50]

Delineating the maxillary spread pattern is quite difficult, because limited data is available regarding its infections.[3] Nevertheless, it is plausible to consider that the observed difference in the spread profile between maxillary and mandibular infections may be due to differences in the distance between the original focal area in jaw bones and each of the spaces. For instance, maxillary infection was associated with temporalis muscle involvement more often than mandibular infection. Maxillary infection also spreads first to the masticatory space, but the temporalis and lateral pterygoid muscles are predominant targets for the infection. Involvement of the sublingual and submandibular spaces is rare. Otherwise, odontogenic infection arising in the mandible spreads first to the masticatory space. The masseter and medial pterygoid muscles in the masticatory space are most frequently involved. Thereafter, the infection spreads medially into the parapharyngeal space and posteriorly into the parotid space. Involvement of the sublingual and submandibular spaces seems to occur directly from the primary site of mandibular infection.[3]

There are complex pathways which allow infection to spread along the facial and neck structures. Thus, it is important for dental practitioners to know more about the possibility of a dental intervention to be a cause of severe infections.

The sequence of odontogenic infection spread that most commonly occurs is:

  1. The masticatory space is the primary site of spread from mandibular infection.

  2. The parotid and pharyngeal spaces are the secondary sites of spread from the masticatory space.

  3. Mandibular infection spreads directly to the sublingual and submandibular spaces, and

  4. Maxillary infection spreads to the deep facial and neck spaces in a different way from that of mandibular infection (Figure 2).

5.2. Fascial infections derived from maxillary odontogenic origins

The pattern of maxillary infection spread differs from that of the mandible. Generally, the main maxillary spaces involved were found to be the buccal maxillary (19.05%) and canine (15.24%).[49] According to Yonetsu et al., the temporalis muscle was involved in 100% of the patients with maxillary infection. The involvement of the temporalis muscle in mandibular infections occurred only in 26% of the patients. The downward spread into the sublingual and submandibular spaces from maxillary infections did not occur. The lateral pterygoid and masseter muscles were frequently involved (86%) as in the cases of mandibular infection. Other spaces were also involved, but less frequently. The buccal space was involved in 57% of the patients with maxillary infection[66] (Figure 2).


Figure 2.

Different locations of odontogenic infections. (A) Submandibular and sublingual region. (B) Submandibular region. (C) Cervical region. (D) Palate. (E) Orbital region. (F) Submandibular and buccal region.

6. Causes of infections

6.1. Pericoronitis

Pericoronitis is an infection of the gingiva of a partially erupted tooth. The most frequent form of pericoronitis is caused by the partially erupted lower third molar, mainly due to the favorable niche that is created once the mucous cap covering the molar becomes retentive and deep enough to trap food particles and reduce the oxygen potential. These factors create the perfect microenvironment for the onset and subsequent development of a recurrent infectious, inflammatory condition caused by polymicrobial microorganisms, especially strict anaerobes.[19] Third molar pericoronitis may appear in either of its two acute variations, namely serous and suppurative, as well as in its chronic form; when either of the two acute forms previously mentioned stays untreated.

6.2. Periapical lesions/Intra-oral abscess

The most significant clinical condition of all bacterial infections of periapical origin is the so-called acute apical periodontitis.[16] It is usually the result of purulent pulpitis that spreads into the periapical space, therefore, it appears in the course of pulpal disease. In acute apical periodontitis there is an accumulation of pus inside the apical space of the tooth involved. This condition is commonly underestimated by dental practitioners in terms of its morbidity and mortality.[46] (Figure 3)


Figure 3.

Clinical (A) and radiographic(B) aspects of a periapical lesion.

6.3. Infection of sublingual, submental and submandibular spaces (Ludwig’s Angina)

Ludwig’s angina is a rapidly spreading cellulitis that may produce upper airway obstruction, often leading to death. The most common source of Ludwig’s angina is an odontogenic infection, from one or more grossly decayed, infected teeth, and is usually as a result of a native oral mixed aerobic-anaerobic flora. The patient with Ludwig’s angina presents severe and obvious extra oral swellings including bilateral submandibular, submental, and sublingual spaces. Elevation and displacement of the tongue, trismus, drooling of saliva, airway obstruction, sore throat, dysphagia and/or dyspnea are commonly present. With extensive use of drainage and antibiotics, most facial infections have satisfactory outcome before they have a chance to progress to Ludwig’s angina.[1] (Figure 4)


Figure 4.

Clinical presentation of Ludwig’s angina.

6.4. Cervical cellutis

Cervical cellulitis is most commonly from odontogenic origin and despite modern antibiotic therapy, cases with an initial delay in diagnosis and treatment may still result in this life-threatening situation.[17, 58-60] Odontogenic infections are usually locally confined, self-limiting processes. However, under certain circumstances, like anatomical variations or suppression of the immune system of some patients, these infections may pass through the bony, muscular, and mucosal barriers and spread into contiguous and distant spaces, resulting in severe fulminating infections in the body cavities.[60]

When cervical cellulitis involves the parapharyngeal, retropharyngeal, and viscerovascular spaces, the purulent process has easy access to the mediastinum, pericardium, and thorax, thereby increasing mortality rates.[13, 17, 58-60] Because of the fulminant nature of descending cervical cellulitis with mediastinal complications, prompt recognition followed by broad-spectrum antibiotic therapy, immediate surgical intervention, and intensive medical support are required.[13, 61]

The second and third mandibular molars are the teeth most frequently implicated in the cause of odontogenic deep neck infections.[17, 58, 60, 61] Because their roots lie below the mylohyoid muscle, medial perforation of a periapical abscess has immediate access to the submandibular space. Then, a collection of pus in the neck spreads along the cervical fascial planes, resulting in complications.[13]

6.5. Descending Necrotizing Mediastinitis (DNM)

Acute purulent mediastinitis occasionally develops as a complication of odontogenic infection, in which case it is denominated descending necrotizing mediastinitis.[17] This is a serious infection involving the connective tissue that fills the interpleural spaces and surrounds the median thoracic organs. It is one of the most dreaded and the most lethal form of mediastinitis, which occurs as a complication of oropharyngeal abscesses or as a complication of cervical trauma, with severe cervical infection spreading along the fascial planes into the mediastinum. As infection spreads along deep cervical fascial planes into the mediastinum, widespread cellulitis, necrosis, abscess formation, and sepsis may concomitantly occur. The delay of diagnosis and late or incomplete drainage of the mediastinum are the main causes for high mortality rates associated with this condition.[4]

Even with the use of computed tomography scanning or magnetic resonance examination, aggressive drainage, and modern antibiotic treatment, the mortality rate of descending necrotizing mediastinitis remains high. Surgical management, particularly the optimal form of mediastinal drainage, remains controversial with support ranging from cervical drainage alone to cervical drainage and routine thoracotomy.

6.6. Necrotizing fasciitis

Abscesses of the peritonsillar region are among the most common deep abscesses of the head and neck. Although rare, complications resulting from this disease may be life threatening. One of the most dangerous complications is necrotizing fasciitis, which is a rare soft tissue infection characterized by progressive destruction of fascia and adipose tissue that may not involve the skin.[62, 63] Necrotizing fasciitis is characterized by its fulminating, devastating, and rapid-progressing course.[64] Diabetes mellitus, burns and malnutrition are common predisposing factors. Initially, cervical necrotizing fasciitis is predominantly characterized by a “simple” infection in the upper aerodigestive tract like pharyngitis or even tonsillitis. Typically, the general condition gets worse within a very short period of time with cardiovascular decompensation due to a toxic shock-like condition. Cervical necrotizing fasciitis initially involves the superficial muscular system and superficial fascial planes of the head and neck or it may result from a deep soft tissue infection, such as odontogenic infections or even pharyngitis, which spreads along the deep fascial planes.

If the disease is not recognized in time the infection can rapidly involve the great vessels or mediastinum, producing systemic toxicity and sepsis.[65, 66] The basis of successful treatment comprises aggressive surgical debridement and drainage of the involved necrotic fascia and tissue along with intensive broad-spectrum intravenous antibiotic coverage.[63]

7. Signs and symptoms

The current signs and symptoms presented by patients with severe infections from odontogenic origin are crucial factors for the patient’s life maintenance. Sato et al., has shown in their eight-year retrospective study that cases of odontogenic infections call for immediate therapeutics, either clinical or surgical, with precise daily or long-term monitoring of patients until complete resolution of the clinical infection status is reached. The most frequent signs and symptoms found in these patients were trismus (43.33%), fever (28.10%), dysphagy (25.24%), pain (24.76%), and swelling (20%), all of which are classic signs of a dire clinical situation.26

8. Imaging

Imaging plays an essential role in the diagnosis and management of head and neck infections since, by clinical examination alone. It is often difficult to determine if a swollen neck is due to cellulitis or an abscess; the location, extent or source of the infection, and whether the process is self-limited or if it is potentially life-threatening is also clinically unclear.[21]

Radiographs of the cervical segment and the chest may be useful in the demonstration of subcutaneous emphysema in the form of vertical, linear, clear bands of gas extending from the cervical spaces into the mediastinum. The lateral radiograph of the neck can reveal a prevertebral soft tissue opacity pushing the trachea anteriorly. Chest radiograph can demonstrate a widened mediastinum and pleural effusion. However, the modest diagnostic sensibility of cervical and chest plain film should call immediately for computed tomography scanning or a magnetic resonance of the cervicothoracic areas.[2, 17, 67, 68]

Any patient with neck swelling and/or pain from dental infection should have a computed tomography exam of the neck and chest to evaluate the spread of infection. Computed tomography examination and neck evaluation include: diffuse thickening of the cutis and subcutis and reticular enhancement of the subcutaneous fat of the face and neck; thickening and/or enhancement of cervical fasciae; asymmetric thickening or enhancement of cervical muscles, reactive lymphadenopathy; septic vascular thrombosis and fluid collections with or without gas. Mediastinal computed tomography findings include: streaky enhancement of mediastinal fat, fluid collections with or without gas, pericardial effusion and pleural effusion.[21]

9. Treatment

Treatment of odontogenic infections includes diagnosis and management of the causative factor, drainage when necessary (Figures 5-6) and, usually, prescription of appropriate antibiotics. It is imperative that the source of infection be addressed immediately. In addition, the patient’s medical status must be optimized. The patient’s fluid and nutrition status should also be addressed, as many patients with odontogenic infections have decreased oral intake due to pain and difficulty in chewing or swallowing. The clinician must be aware of the most likely causative organisms and prescribe the narrowest spectrum of antibiotics that will cover all possible offending organisms.


Figure 5.

Sequence of drainage of odontogenic infection – case 1. Note that the most dependent part (under the swelling) must be incised not the thin most swollen part (to prevent scarring).


Figure 6.

Figure 6: Sequence of drainage of odontogenic infection – case 2.

10. Conclusions

A simple tooth infection, especially in diabetics, immunocompromised, or debilitated patients should not be underestimated in its ability to cause severe infections. Furthermore, even non-invasive dental manipulations may also precipitate systemic spread. Facial and cervical infections are potentially lethal complications. However, with good knowledge of the anatomic pathways of the infection, early diagnosis, attention to airway maintenance, aggressive intravenous antibiotic therapy, surgical intervention and careful postoperative management, the infectious process should have a satisfactory outcome. The practitioner must be alert to the particularities of infections from odontogenic origin, as well as to the facial and cervical spaces anatomy, because these structures are crucial for the patient’s life and play important roles during the execution of treatment procedures.


The authors would like to thank Analice Giovani Pereira for the support during the writing of the chapter and selection of clinical cases.


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