The regional distribution of the authors
Glaucomatocyclitic crisis was initially described in detail by Posner and Schlossman in 1948, so it was also called Posner – Schlossman syndrome (PSS). PSS is a special form of anterior uveitis with glaucoma, mainly seen in young adults, characterized by non-granulomatous iridocyclitis with significant elevation of intraocular pressure. In most cases, the disease took a form of acute, recurrent and monocular onset. [1, 2]
This disease is often seen in people aged from 20 to 50, and rarely in people above 60 years old. 5% or less of PSS cases were reported in people above 60 years old . The disease is rare in Western countries, it was reported that 19 in one million people have suffered from PSS in Fenland . As PSS is a kind of disease attacks intermittently,It is difficult to diagnose PSS in intermittent period for the lack of diagnostic signs and investigate the morbidity with epidemiology methods.We used the full text VIP Chinese literature retrieval system and Medeline retrieval system to find PSS reports from 1975 to 2011 in both English and Chinese literature and divided into review, case, experimental study and clinical report four categories,then analysed the regional distribution of the authors and cases (Chinese reports were divided into the Yangtze river and the other, English reports were divided into Asia and the other).
Chose the report which contained the most number of cases if there were more than two from the same author. Statistical results shows that 1262 cases were reported by 33 chinese clinical reports in which 991 cases reported by 20 reports from the area near the Yangtze river,and 271 cases reported by 13 reports from the other area. 211 cases were reported by 16 English clinical reports in which 144 cases reported by 7 reports from the asia area and 67 cases reported by 9 reports from the other area. The results above suggest that there are much more literature and cases related to PSS in the area near the Yangtze river and infer that the prevalence of PSS in that area may be higher.
|Chinese||Near the Yangtze river basin||0||11||1||20||32|
1.3. Possible etiology
Many factors were considered to be related to the onset of PSS, such as allergy, fatigue, mental fatigue, mental stress, decreased body resistance, infection, hypothalamic disorders, autonomic dysfunction, abnormal reactions of ciliary vascular and nervous system and abnormal development in angle of anterior chamber.
Recent research had confirmed that concentration of prostaglandins,(PGs) in the anterior chamber aqueous increased obviously in the PSS cases, especially that of PGE. 
Infection by herpes virus.
The conclusion that PSS was caused by herpes simplex virus (HKS) was reported by Yainamotos in 1995, and was confirmed by many following researches. A recent report showed that antiviral treatment reduced the frequency of the outbreak of the disease. [6-7]
It was reported that aqueous humor of a binocular PSS case were collected after suffering from herpes viral keratitis for five months with anterior chamber paracentesis, then DNA of cytomegalovirus (CMV) and HKS were measured by means of quantitative polymerase chain reaction( PCR), the results showed CMV was positive but HKS was negative. It was speculated that CMV which belongs to herpes virus genera would also leads to PSS like as wise. It was considered that PSS is not a separate disease, but a kind of anterior uveitis relating to infections of herpes virus.
A study from Singapore showed that the CMV DNA of aqueous humor was positive for 24 of 104 anterior uveitis cases with monocular high IOP, in which 18 cases were PSS, 5 cases were Fuchs heterochromic iridocyclitis (FHI). Another study showed CMV DNA was positive in 35 of 67 PSS cases (52.2%), 15 of 35 FHI cases (41.7%). Although the kerato-precipitates (KP) in CMV DNA positive anterior uveitis cases was consider to be accompanied with endothelial halo,clinical difference was not so significant between CMV DNA positive and negative cases as less aqueous humorin sample and weak sensitivity of detection method. In 2008, aqueous analysis for CMV by PCR was performed in 103 eyes of 102 patients with presumed PSS or FHI at the Singapore National Eye Centre. Their records were reviewed for clinical features and human immunodeficiency virus (HIV) status of the CMV-positive patients. The main parameters were age, gender, maximum intraocular pressure, endothelial cell count, endothelial changes, PCR results, and presence of uveitic cataract and/or glaucoma. It was found that there was no clinically detectable differences between CMV-positive and negative presumed PSS eyes. CMV-positive presumed FHI patients are more likely to be male, older at diagnosis or have nodular endothelial lesions. 
Helicobacter pylori infection.
It was reported in South Korean that there was a significant difference of the positive rate of helicobacter pylori serum antibody between cases with PSS (80%) and cases without PSS(56.2%). In another prospective study, 40 cases with PSS and 73 cases without PSS received serologic analysis for the presence of H. pylori infection by an enzyme-linked immunosorbent assay. Positive rate of serum anti-H. pylori IgG was compared between the two groups. It was proved that H. pylori infection occurred significantly more often in PSS patients. This study suggests that exposure to H. pylori infection is associated with PSS in Korea. 
In most cases, the disease always attacks the identical eye repeatedly, binocularly affected cases is not common;
PSS result in paroxysmal increase of IOP repeatedly,which reaches as high as 40 to 60 mmHg, and lasts for 1 to 14 days generally,1 month occasionally,2 months rarely, interval of onset is from months to 2 years;
Symptoms are not obvious, just mild discomfort for most cases;
Eyesight is normal generally, blurred when suffer from corneal edema at onset;
Pupil becomes bigger slightly with normal reaction to light, and never adheres to lens;
The KP of PSS appeared in a few days after or before the elevation of IOP with number of 1 to 25, took a form of hoar and suet-shaped and disappeared days to 1 month after the IOP returned normal , distributed mainly in the inferior part of the cornea or concealed in the trabecular meshwork. There were no or at most a few planktonic cells in aqueous while the flare was negative .There is no inflammatory cell in vitreous body ( See Figure 1);
The anterior chamber angle is open, no matter IOP is normal or elevated;
Visual field and fundus of most cases is normal generally, but a reversible expanding of vascular shadow may occur during an acute onset;
Coefficient of outflow facility (C value) descends in episodes and recovery as IOP in intermission; various stimulation tests for glaucoma are negative in intermission.
The forms of onset of PSS could be divided into three kinds: KP, high IOP and intermediate type, according to relationship between KP and IOP.
The patient complained of her blurred vision two months ago, examination in other hospital showed: conjunctiva of her left eye wasn’t congestive and the cornea was edematous mildly, IOP: 34/ 18(R/L) mmHg; there were some round lipid-like KP in the left cornea, aqueous flare (-). She came to our hospital on June 7, 2012, ophthalmologic examination: vision was 0.5/ 1.5(R/L), best corrected vision of left eye was 1.2(-1.25DS), IOP: 18/ 13 (R/L) mmHg. Her right eye was normal, conjunctiva of her left eye wasn’t congestive and there were five rounds lipid-like KP in the left cornea, binocular C/D was 0.4. Her KP faded away after the treatment of chloromethyl and pranopulin (three times a day) for three weeks. Examination of FFA, ICGA and Virus screening were normal on July 10.The measurement of her 24 hours IOP performed two weeks after she ceased the drugs was 20-14mmHg(R), 15-12 mmHg (L). The result of her visual field and the OCT for glaucoma was normal. She was diagnosed as PSS in left eye and suggested to be observed and treated timely.
1.5. Treatment of typical cases in episodes
Anti-inflammation: Corticosteroid drugs is needed in most cases, but it should not be used too long a time, so as not to cause the corticosteroid glaucoma.
It is a better select in some cases to apply non-steroidal anti-inflammatory drugs (NSAIDs) such as eye drops of pranoprofen, indomethacin and flufenamic acid.
Reducing IOP: Eye drops of epinephrine, timolol,or clonidine was needed singly or jointly for common patient, carbonic anhydrase inhibitor orally when the IOP is higher than 30mmHg and mannitol of intravenous drip when the IOP is higher than 40mmHg.
The antiviral treatment systemically or implanting long-acting agents maybe helpful to reduce the frequency of attack, but it has worrying and serious side effects and cost too much. 
2. The dispute and problems about prognosis
It was considered in the early years that PSS have a favorable prognosis without glaucomatous damage of optic disk and visual field, however, a number of authors have confirmed that part of the PSS cases suffered from glaucomatous damage similar to that in primary glaucoma patients in recent years. A lot of questions remained vague such as monocular or binocular, age of onset, the detailed features of its IOP and KP, the incidence and degree and relating factors of glaucomatous damage, especially the clinical approaches via which the damage occurred and disease complicated with PSS. These brought about to two undesirable consequences: first, PSS patients were misdiagnosed as primary glaucoma and received incorrect treatment even led to serious adverse consequences due to the lack of knowledge on the clinical characteristics of PSS.On the other hand, most cases of PSS combined with primary glaucoma patients especially these with primary angle-closed glaucoma were failed to be diagnosed correctly without delay, thus the best opportunity of treatment lost ; severe damage resulted in.
In order to solve the problems mentioned above, we have made a long-term systematic clinical study about PSS for more than 20 years persistently.
3. The main results of our clinical research
The main results of our clinical research included 4 fields as following: the clinical characteristics of PSS; the glaucomatous optic nerve damage in PSS patients; the clinical approach of optic nerve damage in PSS patients; other diseases concomitant with PSS.
3.1. Study on the clinical characteristics of the PSS
The research about clinical characteristics of the PSS included four aspects: clinical observation and analyzation of monocular primary open-angle glaucoma(POAG) and binocular PSS; clinical features of elderly PSS patients; characteristics and clinical value of the intraocular pressure and the C- value in PSS patients ; the characteristic of postural intraocular pressure change in PSS patients.
3.1.1. Clinical observation and analyzation of monocular primary open-angle glaucoma and binocular PSS
A long-term, systematic clinical observation and analysis were completed on 121 cases with tentative diagnosis of POAG (22 cases of monocular) and 126 cases of PSS (17 cases of which was binocular). (See figure2)
Glaucomatous visual field damage of monocular/ binocular PSS and binocular POAG
Analyzation of the clinical data of patients without doubt with the chi-square test showed: 1) The incidence of glaucomatous visual field damage in binocular PSS (15/16) was much higher than that in monocular cases(30/85), (X2 =27.43, P<0.01). 2) The damage in 26 of 30 monocular cases were in early stage, while that in 9 of 15 binocular cases were in middle/ last stage, the difference was significant(X2 =3.53, P<0.01).3) There is no significant difference in incidence and degree of glaucomatous visual field damage between binocular PSS and binocular POAG. (See Table 2)
Visual field damage in binocular PSS
15 of 17 binocular PSS cases were confirmed with glaucomatous visual field damage, that was much more serious than in monocular cases; however, no remarkable difference was found between the course of disease in monocular and binocular cases. (See Figure3)
The result suggests that the course of disease cannot explain the severity of visual field damage in binocular PSS. We speculate that binocular PSS may be more relevant to POAG essentially through the following two ways.First, the insufficiency in adjusting IOP result in combination with POAG in some cases; secondly, the weak resistance of optic nerve to high IOP make it ease for a cumulative effect of high intraocular pressure during attacks of pure PSS to bring about visual field damage.
Results of clinical follow-up to monocular POAG
The results of clinical follow-up observation on the 22 cases with clinically suspected monocular POAG is as follows: 15 of the 22 cases were confirmed not to be POAG, 9 of them had been proved to be PSS. Although no definite diagnoses was made in the other 7 cases,but clinical manifestations contradictory with POAG were found in most cases, 3 of them were suspected of PSS.(See Figure4)
The result suggests that the diagnosis of monocular POAG should be very careful, in addition to angle closure glaucoma and other secondary glaucoma, PSS which appears late or last transitorily should not be ignored. Close attention to slit lamp examination for KP and its relationship with IOP should be paid for such cases.
All in all, it cannot be stated too strongly: we should be very deliberative when making a diagnose of monocular POAG or binocular PSS, as half part of suspicious monocular POAG cases were confirmed with PSS after clinical follow-up, and there was a closer connection between binocular PSS and POAG. 
3.1.2. Clinical observation of aged PSS cases
3.1.3. The characteristics and clinical value of the intraocular pressure and the C- value in PSS cases
Crossed-over phenomenon of binocular IOP and C- value had not appeared in the control group (primary glaucoma) as well as Group C (PSS combined with POAG).
3.1.4. The characteristics of postural IOP change in PSS cases
3.2. The visual field damage in PSS cases
Although reports about that glaucomatous optical neural damage occurred in some cases of PSS were constantly released for past twenty years, we saw little of the systematic research aimed at the incidence, severity and probable relating facts of the damage. [3, 9]
3.2.1. Incidence and severity of the damage
3.2.2. The characteristic of the visual field damage in PSS
3.2.3. Relating factors of the visual field damage in PSS
Methods: Analysis the clinical data of 145 PSS cases and 166 POAG cases for recent 15 years. Results about the incidence and severity of visual field damage in the two kinds of glaucoma had been showed above.
3.3. The clinical approach of optic nerve damage in Posner Schlossman syndrome
In recent years a number of authors have confirmed that glaucomatous optic nerve damage similar to that in primary glaucoma cases occurred in part of the PSS cases, but the clinical approach of the occurrence was not reported. Clinical data of cases with PSS during a period of 25 years in our hospital was collected and analyzed, and four clinical approaches via which the damage occurred in PSS cases were deduced.
To investigate the clinical approach of optic nerve damage in PSS.
208 cases with PSS during the recent 25 years collected in our hospital(male 124 cases, female 84 cases), from 9 to 71 years old, with an average of 39.56±12.80. Diagnosis standard for PSS was basically accorded to clinical features described by Posner and Schlossman, except for the cases who suffered binocularly or had damage were contained in. [23, 26]
History, eyesight, intraocular pressure of episode and intermission, depth of anterior chamber, gonioscope or UBM, intraocular pressure during 24 hours in intermission without eyedrops more than five days, panretinalscope or OCT, FFA in episode of part cases, and so on.
Analysis for damage
Standard: repeatable glaucomatous visual field damage and corresponding fundus performance
Stage division standard of glaucomatous visual field damage(see Table3)
|Without defect||static visual field: no more than 2 spots with sensitivity reduces more than 5dB , no spot with sensitivity reduces more thandB; dynamic visual field: no nasal step and temporal more than 10 degrees, no significantly constriction of visual field (except for refractive interstitial lesions and retinopathy)|
|Early stage||paracentral scotoma, nasal step, , arcuate scotoma not linked with physiological blind spot|
|Moderate stage||arcuate scotoma linked with physiological blind spot, nasal hemianopsia,ring scotoma, constriction of visual field more than 30 degrees,|
|Absolute stage||no light perception|
According to the results of comprehensive and dynamical analyzation to the clinical data of each cases and classification method shows as table 4, each case was discriminated for the clinical approach of optic nerve damage. [20,21,22,24,27,28]
|Age of onset||middle-aged and aged people||middle-aged and aged people||similar to POAG||middle-aged and aged people|
|Family history of glaucoma||usually not||usually not||sometimes have||most have|
|Monocular/||monocular||monocular||binocular or monocular||monocular KP,|
binocular high IOP
|Typical PSS course||positive||positive||positive||negative||Intermittent attack with KP||positive||negative|
|Cross phenomenon of intraocular pressure||positive||positive||negative||negative||negative||positive */ negative||positive */ negative|
|Intraocular pressure of 24 hours in period of intermittent||normal||normal||normal||abnormal||abnormal||abnormal||abnormal */ normal||abnormal */ normal|
|Anterior chamber depth||normal||normal||normal||normal||normal||normal||A little shallow||Very shallow|
|Anterior chamber angle||medium width||medium width||medium width||medium width||medium width||medium width||Narrow II-III||Narrow III-IV|
Incidence and stage distribution of glaucomatous optic nerve damage
190 cases of 208 patients with PSS had a set of complete material. There were 71 cases (34.1%) with optic nerve damage, in which 12 cases (16.9%) regarded as suspicious damage, 59 cases (83.1%) regarded as definite damage.
Stage distribution of glaucomatous optic nerve damage was shown in Table 5:
The clinical approach of optic nerve damage
Four clinical approaches via which the damage occurred in PSS were deduced, they were represented as Type A, B, C and D.
Type A Cumulative effect of repeated episode of high intraocular pressure of pure PSS leads to visual field damage: 27 cases
Type B Recurrent attacks of PSS which results in secondary trabecular meshwork damage causes secondary open-angle glaucoma: 6 cases
Type C PSS combined with primary open-angle glaucoma: 19 cases
Type D PSS combined with primary closed-angle glaucoma: 7 cases
Composition of the clinical approach in 59 cases regarded as definite glaucomatous optic nerve damage was showed in Figure10.
Distribution of stage of visual field damage in different optic nerve damage approaches was showed in Table 6
There is not significant difference in the stage distribution of visual field damage in different type of PSS patients. ( X2 =6.904, P>0.05).Make the early and moderate stage as one group, advanced and absolute stage as anothe group, Statistical result shows that there is significant difference in the stage distribution of visual field damage in different type of PSS patients.The incidence of early stage of glaucomatous visual field damage in Type A (63%) was higher.While 7 of 19 Type C cases were in advanced stage.
The clinical approach of optic nerve damage in Posner-Schlossman syndrome.
In the past PSS was considered to be a self-limited disease and has a favorable prognosis,however, in recent years a number of authors have confirmed that part of the PSS cases suffered glaucomatous optic nerve damage similar to those in primary glaucoma cases, but the incidence, degree, related factors and clinical approach of the occurrence is unknown. This part focused on the clinical approach of optic nerve damage in Posner-Schlossman syndrome after aforementioned researches. Report about optic nerve damage caused by PSS combined with primary open-angle glaucoma is common; the other types were seldomly reported.Systematic research aimed at this question has never been seen so far at home and abroad. We determined the damage approach by analyzing each patient's clinical data dynamically and comprehensively according to the discrimination method established on the basis of relating literatures and the results of our long-term systematic study, and got the conclusion that there were four clinical approaches via which the damage occurred. Beyond all question, further researches, supplement and correct is necessary in this field, but the method and result of our study maybe a wind vane for the further researches.
Clinical features and treatment principle for cases with damage from different clinical approach
188.8.131.52. Type A Cumulative effect of repeated episodes of high intraocular pressure of pure PSS leads to damage
Except for visual field damage, type A cases complied with the basic characteristics of typical PSS: monocular attacked; intermittently onset of high intraocular pressure with hoar and suet-shaped KP ;normal intraocular pressure(including 24 hours intraocular pressure )of the fellow eye in episode and the both eyes in intermission ; Crossed-over phenomenon and postures change of IOP; Normal anterior chamber depth; wide anterior chamber angle; Visual field change of vascular shadow usually appears in episode and recover in intermission at the initial in most cases, and true visual field damage is of mild and early stage usually , but loss of light perception can be seen in a few cases; the attack lasts a long time frequently in middle-aged and aged people for long course, also with higher IOP; heterochromia iridis occurred in later stage in some cases. (See Figure11) [20, 22, 29]
Pay enough attention to treatment for each attack, in which the most important is controlling intraocular pressure timely and effectively. Surgery is necessary for the cases with excessive frequent attacks, heavy damage or obvious progress of his damage.
The surgery method and the time: glaucoma valve or EX-press glaucoma filtration device implantation maybe suit for cases with excessive frequent attack, high IOP but light inflammation (intermission or episodes); trabeculectomy could be selected for cases with low attack frequency, high IOP as well as severe inflammation (intermission only).
1) She visited our hospital and was diagnosed as glaucomatocyclitis crisis of left eye in other hospital six years ago. In the initial stage, she attacked once or twice per year with duration of 3~7 days for each attack and ceased spontaneously, then the frequency of attack increased and the duration extended. This attack happened one month before this visits to our hospital and stop one week ago without use of any drug.
Examination at first visit: Vision 1.0(OU), IOP19.7mmHg(R), 12mmHg (L), anterior chambers of both eyes were not shallow, iris color was symmetrical, KP (-).
Fundus examination: C/D0.3(R) 0.6(L), there wasn’t other abnormalities. She was diagnosed as secondary glaucoma of left eye. On September 13 (10 days after withdrawal), the 24 hours IOP of both eyes were measured: right eye: 14-18mmHg, left eye 12-14mmHg, Corneal thickness: right eye: 584µm, left eye: 575µm. She was diagnosed as “glaucomatocyclitis crisis in left eye.”
Another onset lasted for more than 10 days, IOP of the left eye was 43mmHg, there was 2 hoar and suet--like KP and faded iris pigment in left eye. There were total seven attacks in oneyear, with the duration from 1 week to 20 days, during one of which the KP appeared 9 day after the occurrence. 24 hours IOP during this episode: right Eye: 14-19mmHg, left Eye: 23-29mmHg; iris depigmentation of her left eye exacerbated, no abnormal was found with fundus angiography. The recent onset occurred in September this year, the medication of hormone and pranopulin continued for 3 months, with another minor attack during that this period.
She made another visit to our hospital one year later. It was found that the iris of her left eye appeared a typical “rain dozen sand samples”, meanwhile, there were two off-white round medium-sized lipid-like KP.and she was diagnosed as "left eye glaucomatocyclitic crisis with heterochromatic iris.” Since then, the attack occurred more frequently, with frequency of 1 to 2 times per month, the visual field damage exacerbated. She was hospitalized in our department, and the surgery of glaucoma valve implantation was performed. Postoperative intraocular pressure: 19mmHg for her right eye and 6mmHg for her left eye:, visual acuity:: 1.0 left eye (with pink hole) for her both eye, and the syndrome did not attack postoperation. (Clinical data please see Figure 12)
2) He was hospitalized in our hospital for the reason of “intermittent pain of left eye for 25 years, decrease of vision for 20 years, blind for 1 year”.
Since 25 years ago, the patient got intermittent episodes of pain and blurred vision with his left eye, which occurred 1 to 2 times per month with the duration of 3to 5 days, and can be self-cured. In many hospitals he was diagnosed as “glaucomatocyclitic crisis” and treated with irregular medication. The occurrence becomes more frequently in the recent 10 years, and the duration longer, and the vision recessions gradually.
In the intermittent period, he was hospitalized for systematic examination. Visual acuity was 1.0 for his right eye and no light perception for his left eye. All the results of IOP, tonography, 24 hours IOP measurement and other tests during the intermittent period were normal for his both eyes.
The result of the medical examination at this hospitalization showed as fellowing: his right eye had a corrected visual acuity of 1.0, IOP 14mmHg, C/D 0.4, wide anterior chamber angle; his left eye had no photoreception, intraocular pressure 56mmHg, C / D1.0, width of N1 ~ N3 for the anterior chamber angle with some small limited adhesions; corneal edema, a dozen of round lipid-like KP.
Without any treatment, the IOP of his fell to 14mmHg within one week. All results of examinations including 24 hours IOP measurement, drinking water experiment, darkroom prone test for his right eye were normal. Laboratory results of systemic body check were normal.
His left eye still had attacks of PSS after he left hospital and each attack could be self-cured. IOP and 24-hour IOP during the intermittent period were measured to be normal, and his left eye had an IOP lower than that of his right eye, a typical IOP cross phenomenon appeared every time. Three years later, the fundus and visual field of his right eye kept normal. (Clinical data see Figure 13)
184.108.40.206. Type B secondary open-angle glaucoma from secondary damage to trabecular meshwork by recurrent attacks of PSS
Type B cases complied with the basic characteristics (above mentioned) of typical PSS in early stage. These characteristics lost eventually as the damage to trabecular meshwork gradually accelerated, the attack takes place more frequently and lasts a longer and longer time with a higher and higher IOP, and serious visual field damage developed at last. [30, 31] However, the fundus, visual field, IOP in intermittent and episode of the fellow eye maintained normal. Patients of this type usually had a long course of the disease with an order age.
It is necessary to reduce IOP with drugs according to extent and characteristics of elevated IOP and diminish inflammation with hormone of weak effect on elevating IOP for short time, for example, lotemax. PGA is useful and myotic is prohibitive. Surgery or other treatment (SLT, trabeculectom, glaucoma valve or EX-press implantation) should be taken into account according to the IOP level controlled by drugs in intermittent and the situation of visual field damage.
He was diagnosed as “left eye PSS” with the complain of vision decline associated with distending pain of his left eye in other hospitals five years ago.
The medical records of other hospitals showed: IOP and other relating examinationgs of his right eye in episode and these in intermittent period of his both eyes was normal at the initial stage. The visual acuity decreased gradually, IOP fluctuated from 32 to 48 mmHg in recent years. He was hospitalized in our hospital three times, the results of clinical observation showed: IOP including 24 hours IOP in intermittent period, the fundus and visual field of his right eye appeared normal; while IOP of his left eye was high frequently and higher when PSS attacked, 24 hours IOP in intermittent period appeared abnormal including the highest IOP and IOP variation. The left eye was diagnosed as secondary open-angle glaucoma from secondary damage to trabecular meshwork by recurrent attacks of PSS, and then a trabeculectomy was performed on his left eye. Postoperative IOP of his left eye was from 12 to 10 mmHg in intermittent period, 20 to 31 mmHg in episodes, while his right eye kept normal in all ways. (Clinical data see Figure 14)
220.127.116.11. Type C PSS combined with primary open-angle glaucoma
Monocular/ binocular paroxysmal increased IOP with mild cyclitis; wide anterior chamber angle; binocular abnormal IOP and visual field damage; high average IOP; grate fluctuation of IOP level; absence of IOP cross phenomenon; PSS attacks at the same eye in most cases; at the two eyes alternately or at the same time in a few cases; visual field damage was serious, and more serious in the eye often attacked by PSS. [27, 32]
Enough attention should be given to the treatment for cases of this type, whose incidence reached up to 31% as reported.
Drug treatment is similar to that of POAG, but in episode of PSS, corticosteroid is useful transitorily, while PGA and myotic is prohibitive. Indication of surgery is similar to that of POAG, but classical trabeculectomy should be performed in intermission, and the effect and safety of nonpenetrating trabeculectomy, implantation of Ahmed glaucoma valve or EX-PRESS Glaucoma Filtration Device has not been confirmed. Laser trabeculoplasty( ALT), Selective laser trabeculoplasty (SLT) or Pneumatic trabeculoplasty (PNT) should be adopted in intermission, however, there has not related report. [11, 33, 34, 35]
1) With complaints of discomfort and blurred vision of her left eye for more than 1 year, the patient was diagnosed as POAG in other hospital 10 days ago. Clinical date of that time showed: KP (-), IOP16.3/42.7(R/L), and she was treated with Travoprost Eye Drops to her left eye and brimonidine and brinzolamide to the both eye. 1 week after treatment, her IOP turned to 36/17(R/L), the treatment had been changed to travoprost, brimonidine and brinzolamide for the both eye.
The results of examination in our hospital showed as follows: visual acuity R1.0 (-1.25DS), L0.05(-3.75DS), IOP17(OU); absence of conjunctiva hyperemia; cup/disc ratios 0.8 OD and0.9 OS,and inferior RNFLD(by OCT:) in the both eye; severe glaucomatous visual field damage in both eye.;extended latent time and descended amplitude on VEP; CCT:540/520 (R/L),corneal endothelium cells 1730/2747(R/L); center anterior chamber depth ≥3.0mm and open anterior chamber angle in every direction for the both eye by UBM. She was diagnosed as binocular POAG,and treated successively with travatan, alphagan and brinzolamide to binoculus, but her IOP was not controlled well. Thus, a trabeculectomy was performed the left eye.Two weeks after the operation, the filtration bubble turned fibrosis,and IOP increased. By 3 times of pin-delamination with 5- fluorouracil and eyeball massage, IOP was controlled on 12 to 14 mmHg. Her right eye was treated with travatan, carteolol hydrochloride and brimonidine, IOP was controlled from 12 to 14 mmHg.She was discharged from hospital.
Four months later, the right eye appeared 5 small rounds and mutton-fat like KP, IOP increased to 19mmHg. A week late, KP played down, IOP descended to 12 mmHg. A month later; KP appeared again, IOP increased to 37, after treatment in hospital for a week, the IOP decreased to 12 mmHg. She was diagnosed as POAG combined with PSS. Two months later PSS of her right attacked again, IOP increased to 44 mmHg; visual field damage has progressed remarkably. FFA showed optic atrophy without any other abnormal. She was hospitalized again,and a implantation of Ahmed valve to her right eye was done on the next day. During the operation, the valve appeard out of control; we dealt it well with removable restraint line processing; the IOP and anterior chamber stability was controlled. 2 month after the operation, the IOP increased to 22 mmHg because of the draining disc was packaged. By pin-delamination and eyeball massage, IOP was controlled near to 20mmHg. Carteolol hydrochloride was added and the IOP was controlled well in intermittent, but PSS attacked frequently and the IOP was out of control during episode. she was hospitalized once more and the right eye was treated with no-penetrating glaucoma surgery. 1 month after operation, the IOP was controlled well, binocular IOP was 10mmHg. 2 month after operation, PSS attacked her right eye again, IOP increased to 20 mmHg. This attack faded a week late and IOP of her both maintained 14mmHg below until now. (Clinical data please see Figure 15)
2) She was diagnosed as POAG in other hospitals because of intermittent attacks of distending pain and gradually aggravated blurred vision to her right eye for six years. The left eye has the same symptoms slighter than that of her right eye.
When she was examined in our hospital the results showed as follow: visual acuity: R 0.4, L 0.2; IOP: R 50mmHg and L 17mmHg; anterior chamber angle NI~NII in every direction; The optic cup depressed and enlarged. Argon laser trabeculoplasty was carried out after the diagnosis of POAG. But after that, the right eye relapsed frequently. One year later, the right eye relapsed again. There were three KP which were gray-white, round, and like mutton-fat in the right eye and a wreck of the keratic precipitate in the left eye. After a series of relating examinations such as visual activity, IOP, fundus, visual field, gonioscopy, she was diagnosed as PSS.
Seven years later, the patient attended to our clinic because the same symptoms attacked frequently in recent years and her vision became worse and worse. Attacks appeared as binocular high IOP with binocular KP or binocular high IOP with monocular KP in different time. Clinical data on this visit showed :visual acuity: R 0.2, L 0.15;there has not obvious keratic precipitates in the right eye, but the left eye has one mutton-fat like keratic precipitate; the ratio of C/D was about 0.9; IOP was R 28 mmHg and L 31 mmHg; the visual field has deteriorated over the last few years; 24-hour IOP measurement during the intermittent period showed that IOP of the right eye was from 21 to35mmHg and 23 to 36mmHg for her left eye.Thus,PSS combined with POAG was proved to be the last diagnosis. Her visual acuity and visual field were in a stable condition under regular treatment with carteolol Hydrochloride 2% and brimonidine tartrate as well as anti-inflammatory drug when PSS attacks. (Clinical data see Figure 16)
18.104.22.168. Type D PSS combined with primary closed-angle glaucoma
Except for our data, there had been only two individual reports about PSS combined with PCAG in China and none in abroad. Cases of PSS combined with PCAG at home are much more than those in abroad due to the higher incidence of PCAG as well as PSS at home. In 2004 we reported 6 cases and completed a systematic clinical analysis. It was often reminded by many ophthalmologists that cases of PSS had be mistaken as AACG, but enough attention had not been paid to this type of PSS. [18, 28, 36, 37, 38],
There is a typical history of PSS attack with binocular shallow anterior chamber and narrow or closed anterior chamber angle. PSS hardly attacked synchronously with PACG, the anterior chamber angle is open in episodes of PSS. Type D cases complied with the basic characteristics of typical PSS in early stage: binocular IOP is normal in intermission; with cross phenomenon of IOP; however, when PACG became more advanced, although the IOP of the PSS attacked eye was much higher than that of the unattacked eye in the episode of PSS, binocular IOP turned higher than normal even in intermittent of PSS without obvious cross phenomenon. Most cases were diagnosed as PACG previously, PSS appeared after the treatment for PACG had been completed and the anterior chamber angle been opened, a few cases were typical PSS with narrow anterior chamber angle when they were young; PACG appeared as anterior chamber angle became narrower and narrower with age. Most of the cases of this type were elder with a longer course of PSS and a more advanced visual field damage.
The first is that the anterior chamber angle is open when PSS is diagnosed at episode, either in the intermission of PACG or after PACG was treated with Laser/surgery/drug; the second is that the cases complied with the basic characteristics of typical PSS described by Posner-Schlossman. In our study, 2 cases was diagnosed as PSS at a younger age with binocular narrow anterior chamber angle (first was narrow II, narrow III-IV four years later), 5 cases was diagnosed as PSS after treatment of PACG(similar to the two cases reported at home). [28, 39]
To find out PACG complicated with PSS as soon as possible, it is necessary to carry out a set of comprehensive and careful examinations relating to PACG in the intermission of PSS for PSS patients with factors as follows: the old-aged ,with a serious visual field damage, longer course of the disease, with a shallow anterior chamber or an narrow anterior chamber angle,and binocularly attacked.
When IOP appeared as repeated, intermittent and sudden elevation in a patient with PACG whose anterior chamber angle had been opened and the IOP been controlled well for a period after treatment by means of laser and/or surgery and/or drugs, it is very important to pay sufficient attention to the depth of the binocular anterior chamber and anterior chamber angle on the time the IOP is higher, and to make clinical follow-up observations for KP and its relationship with IOP, so as to ascertain whether PSS is the cause of elevating IOP, so that unnecessary surgery can be avoid.
According to condition of PACG, laser and/or surgery and/or drugs may become options.
Indications of that for cases of PSS combined with PACG is similar to that PACG patients, except for that examination and treatment should be done in the intermission of PSS;
Curative effect on cases with typical cross phenomenon of IOP should be better;
The iris surrounding excision mouth by laser must be thoroughly penetrated and the hole should be big enough;
Corticosteroids and drugs for reducing IOP should be sufficient after laser operation;
It is import to pay attention to the treatment for PSS which continue to attack after laser therapy, and to the monitor of IOP and its dynamic change. Additional drug treatment even trabeculectomy should be adopted timely when necessary;
It is necessary to prevent the attack of PACG in either episodes or intermission of PSS for these untreated PACG cases with the appropriate use of miosis drug.
1) He was diagnosed as "PSS" in our hospital because of pain and discomfort of his right eye,then he was diagnosed as " acute angle-closure glaucoma " in other hospital because of severe sore of his both eyes, and switched to our hospital after remission seven years later.
Examination revealed mutton-fat like KP in the right eye. His right eye was diagnosed as PSS combined with PACG with analysis by synthesis combining history and test results of IOP, fundus, visual field and anterior chamber angle. The right eye was treated with "glaucoma drainage surgery", and the left eye with "YAG laser iridectomy ".
IOP of his both appeared stable for six months after operation, then the right eye was attacked by PSS once again. This attack of PSS appeared as typical KP, open angle and slightly increased IOP. (Clinical data please see Figure 17)
2) The patient came to our clinicbecause of “Repeated intermittent attacks of eye pain and impaired vision for her left eye and right eye as well for more than 14 years”. She was treated with YAG laser iridotomy in other hospital for PACG binocularly twice each.,Her left eye had been still attacked intermittently ever since.Clinical date from her medical record showed that KP and IOP rising appeared nearly simultaneously on each episode and the IOP turned persistently higher than normal even if in intermission since 2 years ago, and the drugs could not control the IOP well.
Examination at this time showed: Vision R 1.0, L 0.4; IOP R 14 mmHg and L 46 mmHg ;2 mutton-fat like KP in the left eye ; shallow anterior chamber and angle multiple adhesions in the both eyes; several trace of lasertherapy on iris of her both eye,the only panetrated hole on the right eye be covered with fibrous membrane, and that on the left eye be too small; cup/disc ratios R 0.4 and L 0.8.A diagnosis of “binocular PACG complicated with PSS in left eye” was established.A complementary lasertherapy was given to her right eye just at that moment; after this lasertherapy,her right had been kept well until now with only the help of 2% Carteolol Hydrochloride Eye Drops twice a day.3 weeks late, when this attack of PSS fade away, she was hospitalized in our hospital,and a trabeculectomy was performed on her left eye, and she was discharged 10 days after a IOP of 14mmHg.6 weeks after the operation, an attack of PSS occurred with a IOP of 32mmHg and lasted a week;such attack occurred once or twice a year after that with a maximal IOP of 25mmHg. The IOP in intermission had maintained near 15mmHg during the first 4 years, but the result of 24h IOP measurement showed 13~20mmHg in the right eye and 15~24mmHg in the left eye. Iris heterochromia appeared in the left eye. Such a therapeutic schedule was established and kept 3 years since then: 2% Carteolol Hydrochloride Eye Drops twice a day to the both eye in intermission of PSS; 2% Carteolol twice a day plus brimonidine 3 times a day with shortly use of Lotemax for the left eye during episode of PSS. IOP of the both eye maintained 15mmHg or below, and the visual field maintained stable in the 3 years.
Several attacks of PSS had been recorded with a IOP up to 40mmHg, and her visual field turned worsen, and “rain dozen sand -like” appearance in the iris of her left eye got more pronounced in the last 2 years. She was hospitalized once more, and another trabeculectomy was performed on the left eye near the first one, at the end of which the two filtering blebs(an original and a just manufactured ) were merged into one. She was discharged with an IOP of 12mmHg; the left eye was no longer attacked after this trabeculectomy ,and the IOP kept stable.
(Clinical data see Figure 18)
4. Main points in diagnosis and treatment of complications of PSS
Other kinds of glaucoma which PSS concurred with or lead to were introduced before. PSS can also concur with or cause iris heterochromia, ischemic optic neuropathy, complicated cataract and other diseases, such as retinal detachment. Main points in diagnosis and treatment of these complications were briefly introduced as follows:
4.1. PSS combined with iris heterochromia
1) The patients came to our hospital because his left eye suffered from intermittent recurrent pain and blurred vision for more than one year. Intraday examinations showed: best corrected visual acuity is 1.0/ 0.6(R/L), IOP: 16.7/ 13.7(R/L) mmHg, FFA in both eyes are normal, optic cup in his left eye is expand. He was suspected of glaucoma. Intermittent recurrent pain and blurred vision kept to attack his left eye for more than half a year after then. These attacks usually ceased a few days late, with or without the help of 0.5% timolol eye drop and other drugs. During this period, the highest IOP record of his left eye was 35mmHg with a normal record of his right eye. The patient returned to our hospital one year later after stopping use of any drugs for two weeks. Ophthalmologic examination at this time showed: visual acuity 1.2 both eyes, IOP 17/15(R/L)mmHg, a lot of small lipid-like KP in the inferior of the left cornea, “rain dozen sand -like” appearance in the iris of his left eye, C/D rate 0.6/0.7(R/L),CCT 553/ 560(R/L). Results of his visual field and OCT showed in Figure below. UBM showed wide-angle in the both eyes. Fundus fluorescein angiography and contrast sensitivity revealed no special finds. 24 hours IOP measurements(2 weeks after KP disappeared): 13~16/ 12~15(R/L) mmHg. Diagnosis of “PSS complicated with iris heterochromia” for his left eye was confirmed than.He was asked to treat every onset of the disease in time with drugs dropping IOP as well as anti-inflammatory medicine. (Clinical data see Figure 19)
2) She was admitted to our hospital because her right eye suffered from repeated episodes of pain with blurred vision for more than nine years, and her vision decreased 3 months, with a primary diagnosis of “secondary glaucoma” for her right eye. A lot of intermittent recurrent pain and blurred vision had attacked her right eye from nine years ago, 2 or 3 times a year. Each attack lasted about one week, than resolved spontaneously. Three months ago her sense of vision went to recession. She felt that her right eye was attacked again recent days, so she can to our hospital. Ophthalmologic examination in this time showed: visual acuity: 0.15/ 1.0 (R/L), IOP: 43/12(R/L) mmHg, mist edema in her cornea of her right eye with a lot of fat-like KP, pale and“rain scatting beach-like” appearance in her left iris with a round pupil about 3mm in diameter, her optic disk appeared pale in color with a C/D 0.9, her anterior chamber is not shallow, ultrasound biomicroscopy (UBM) showed a wide angle in both eye. Her left eye showed no KP with a C/D less 0.3. Her systemic examination and routine inspection and examination showed no special finds. Treatment with drugs dropping IOP such as carteolol and brimonidine and even mannitol as well as anti-inflammatory medicine such as loteprednol kept about a week, KP significantly reduced but the intraocular pressure is still high. Operation of Ahmed valve implantation was performed on her right eye two weeks larer. She was discharged a week postoperative with an IOP of 9mmHg in the operated eye. Her IOP was controlled well with fewer attacks of PSS and a stable visual field in the recent 3 years after the operation. (Clinical data see Figure 20)
Clinical performance of PSS complicated with iris heterochromia
4 cases of PSS complicated with iris heterochromia were reported . They were 2 males and 2 females aged 35 to 45 years. In addition to typical PSS performance, the iris showed “rain scatting sand-like”appearance in all of the 4 patients. All of them are monocular repeatedly attacked at the same eye. Each attack kept 3 to 7 days with a significantly increased IOP up to 30.00 ~ 60.00mnHg and a few of fat-like KP, than relieve itself or extinct with the help of medication. Intraocular pressure (including 24 hours intraocular pressure) in intermittent period appeared normal after discontinuation of all medication with a typical crossed-over phenomenon.
Key-points in the differential diagnosis between PSS complicated with iris heterochromatic and FHI (Fuchs heterochromic iridocyclitis).
The two diseases are different clinically in the following five aspects: the attacked eye and sex of patients, manifestation of intraocular pressure, character of KP, appearance of the Lens and Glaucomatous damage of optic nerve and visual field.
Most of PSS cases were monocular affected, a few of cases was binocularly attacked but alternately between left and right eye, extremely rare cases was both eye attacked simultaneously. Male patient is more than female in PSS. FH is generally believed that no gender differences, more than 90% of the cases was monocularly effected.
The IOP in patients of PSS with iris heterochromatic appeared as an intermittent and abruptly rising when the attack comes with the appearance of typical KP in pure PSS patients. IOP elevation in patients of PSS with iris heterochromatic usually lasted 3 ~ 10days, and then turned to subside spontaneously with the disappearance of the KP after this period, it is also sensitive to drugs dropping IOP and anti- inflammatory medicine. On the contrary, IOP of patient with FH appeared normal in the initial stage for a long time, after that,elevated in part of the cases gradually; however, once the intraocular pressure elevated, it often appeared persistently higher, although there maybe some fluctuations. The elevated IOP and KP in patient with FH had no characteristic of intermittent, were difficult to be controlled and poorly responded to corticosteroids therapy.
IOP in patients with PSS complicated with iris heterochromatic kept the characteristic of crossed-over, that is, the IOP of the attacked eye was higher than that of contra lateral eye during the episode but lower(3 ~ 5mmHg) than the other eye between attacks. IOP in patients with Fuchs syndrome had no such characteristic, once elevated; it is always higher if untreated.
The KP in patient with PSS complicated with iris heterochromia appeared only in a short period during the attack in most cases. This KP is of following characteristics: small round suet-like, medium sized, isolated, with no pigment in initial stage, mainly located in the lower part of the cornea, usually disappeared naturally within a few days after or before IOP reduction. On the contrary, KP in patients with Fuchs syndrome has different characteristics as following: persistence for very long time even always in most cases, white transparent small dot or star-like coexisting with pigmented KP, diffuse distribution in the cornea, sometimes connected each other with fibrous filaments, poor response to corticosteroids therapy. (Clinical data see Figure 21)
Fuchs syndrome complicated with cataract is common at later stage; however the complicated cataract is uncommon in the PSS cases with iris heterochromia.
Glaucomatous damage in PSS cases appeared later and to a lesser extent, however that of FHI cases occur earlier and quicker.
4.2. PSS combined with ischemic optic neuropathy
The patients came to our hospital because her vision of the left eye sudden dropped 2 months ago. She was examined 2 months ago: visual acuity: 1.0/ 0.5(R/L) IOP: 17.3/ 15(R/L) mmHg. The optic disc of her left eye was pale , visual field showed an inferior fan like defect. Fundus fluorescein angiography( FFA) of her left eye showed ischemic optic neuropathy. the anterior segment, fundus, vision, and FFA of her right eye were normal. She was diagnosed as "left eye ischemic optic neuropathy”. She was admitted to our hospital, and examinations showed: visual acuity: 1.0/ 0.15(R/L). IOP: 17.3/ 50.62(R/L), anterior chamber of both eyes were not shallow, Right eye showed no abnormality. Left cornea was mild edema and there was a medium size fat-like KP below the pupil. The boundary of optic papillae in left eye was clear, the color was off white, and the C / D was about 0.3,the angle of left eye was N1 ~ N2. Systemic examination such as X-ray, electrocardiogram and routine laboratory tests were normal. Visual field of right eye was normal and that of the left eye showed a centripetal narrow whit an inferior fan like defect. She was diagnosed as “Left eye PSS,complicated with ischemic optic neuropathy”, and treated with drugs for reducing IOP and nutrition curing to optic nerve for about a weak. She was discharged with IOP 12mmHg disappeared KP, vision 0.2 of her left eye. (Clinical data see Figure 22)
In 2003 1 case of PSS complicated with nonarteritic anterior ischemic optic neuropathy (AION) was reportd. The vision of the case improved significantly after the attack of PSS had been controlled, but the vision and optic neuropathy damaged continually. The authors emphasized that the IOP of PSS patients complicated with AION should be promptly controlled as it is risk factors . It is useful to use drugs with dual role of reducing IOP and improving retinal blood supply in intermittent period.
Our case appeared a sudden vision loss and significant discomfort two months ago. The result of examinations in other hospital such as visual field defect of arcuate below and FFA supported the diagnosis of left eye ischemic optic neuropathy. Results of examinations, reaction to treatment and course of the disease during her hospitalization in our hospital In July 2000 conformed with diagnostic criteria of PSS. The structure of the optic nerve , damage of blood vessels and blood state are related to ischemic optic neuropathy, the severely sudden rising of IOP during attack of PSS maybe the inducing factors. So it is necessary to reduce the IOP during each attack of PSS as soon and effective as possible for the cases of PSS combined with ischemic optic neuropathy or with the risk factors for that.
4.3. PSS combined with rhegmatogenous retinal detachment
He was hospitalized in our hospital for the reason that there was shadow before his right eye with a diagnose of rhegmatogenous retinal detachment.
The IOP of his right eye elevated to 29 mmHg 3 days after hospitalization and a fat-like KP appeared in his right eye, than he was diagnosed as rhegmatogenous retinal detachment combined with PSS. Retinal detachment surgery (Condensation + cerclage + scleral pressure technique) were done after reducing IOP with the treatment of drugs.Postoperative recovery was good. PSS recurrenced 4 months later and recovered 5 days late.
The pathogenesis of PSS combined with rhegmatogenous retinal detachment is unknown. Increased concentration of PG (especially PGE) resulted from retinal S-antigen entered into the vitreous cavity after blood-eye barrier breakdown during the formation of retinal breaks may leads to the inflammation of the uvea, and the higher concentration of PGs and inflammatory products results in the IOP elevation.
4.4. PSS combined with cataract
She complained of recurrent pain and decreased vision of her right eye for four years.
Results of examinations intraday showed: visual acuity:0.08/ 0.4(R/L); corrected visual acuity R:0.3(-0.75DS/1.50DC*111),L: 0.9(-1.25DS/-0.50DC*83 ) ;IOP: 12/ 14(R/L) mmHg; a few of timeworn pigmented KP on the central and lower part of her clear corneal; round pupil about 3mm in diameter; normal iris , opacification of posterior capsule of len; C/D of optic papillae o.4.Her left eye appeared normal.
She was hospitalized with the diagnosis of PSS and was treated with carteolol, brimonidine, mannitol for reducing IOP, tobradex for anti-inflammation and methycobal to maintain optic nerve. She was discharged once the attack of PSS faded away every time.The PSS attacked her 1 to 2 month a time, her vision of right eye declined gradually without other discomfort. (Clinical data see Figure 23)
The possible pathogenesis: repeated onset of IOP elevation and anterior segment inflammation cause disorders of nutrition and metabolism of the lens.
Surgical opportunity: Cataract surgery should be done after the inflammation has been subsidized for more than 3 months. The rest of the indication is the same to the conventional cataract.