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Table of Content

    25 September 2019, Volume 28 Issue 5
    Seventy-year progress in the pharmaceutical treatment of fundus diseases
    ZHOU Nan, WEI Wen-bin
    2019, 28(5):  321-324.  doi:10. 13281/j. cnki. issn.1004-4469. 2019. 05. 001
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    Since the founding of New China 70 years ago, the level of diagnosis and treatment of fundus diseases in China has been rapidly improved. New treatment methods and new drugs have been introduced into China, such as Ranibizumab, Afibercept, dexamethasone sustained-release agents, etc., which has greatly promoted the development of treatment of fundus diseases in China. Especially the emergence of small molecule antibody drugs represented by anti-vascular endothelial growth factor (VEGF) drugs and the promotion of intravitreal injection are milestones in the field of fundus disease treatment, which has changed the previous treatment methods for fundus vascular diseases, reduced the amount of vitrectomy, greatly improved the prognosis of the disease. Homemade humanized recombinant fusion protein Conbercept enriches the spectrum of anti-VEGF drugs. With the development of medicine and diversification of treatment technology for fundus diseases, the treatment level of fundus diseases in China is further in line with the international standards. (Ophthalmol CHN, 2019, 28: 321-324)
    The dilemma and countermeasure of diagnosis and treatment in tuberculous uveitis
    PENG Xiao-yan, MAO Yu
    2019, 28(5):  325-327.  doi:10. 13281/j. cnki. issn.1004-4469. 2019. 05. 002
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    Tuberculous uveitis is a group of inflammatory diseases with different clinical manifestations, which mainly involving the uvea and caused by the direct invasion or immune reaction of tuberculous bacilli. There are many difficulties in diagnosis and treatment of tuberculous uveitis. Since most of the patients with presumed diagnosis of tuberculous uveitis lack of active systemic tuberculosis, to establish an association between this asymptomatic systemic infection and the uveitis carries a great risk of over-diagnosis. The use of etiological or pathological examination of intraocular fluid or tissue is limited by low detection rate and risk of invasive operations. The dilemma of treatment for tuberculous uveitis lies in the lack of culture results of pathogenic bacteria and various adverse toxic effects of anti-tuberculosis drugs. Currently, the main countermeasures to get out of the predicament include understanding of tuberculosis-related examinations, improving diagnostic accuracy of systemic tuberculous, reducing the rate of missed and misdiagnosis of tuberculosis uveitis, and summing up of clinical features of tuberculous uveitis. In addition, the standardized treatment of presumed tuberculous uveitis to retrospectively confirm the diagnosis and improve treatment the prognosis. (Ophthalmol CHN, 2019, 28: 325-327)
    Clinical features and therapeutic outcomes of choroidal tuberculoma
    MAO Yu, PENG Xiao-yan
    2019, 28(5):  336-340.  doi:10. 13281/j. cnki. issn.1004-4469. 2019. 05. 004
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    Objective To observe the clinical features and treatment outcomes of choroidal tuberculoma. Design Retrospective case series. Participants The 7 cases (7 eyes) with choroidal tuberculoma presented to Beijing Tongren Hospital between June 2012 and June 2018. In the 7 patients, 4 were male and 3 were female. Method Best corrected visual acuity, slit lamp ophthalmoscopy, indirect ophthalmoscopy,fundus fluorescein angiography(FFA), indocyanine green fundus angiography (ICGA), optical coherence tomography(OCT), B ultrasound, computed tomography of the chest, Interferon-gamma release assay (IGRA) and Purified Protein Derivative(PPD)were performed. All patients had standard anti-tuberculosis treatment. Treatment outcomes were followed for 6 to 18 months with an average of (11.1±3.8) months. Main Outcome Measures Visual acuity, features of the fundus, FFA and ICGA. Results The average age of 7 cases was (42±11.5) years-old. Three patients had active pulmonary tuberculosis, 2 patient had history of tuberculosis,1 patient had the history of contact with tuberculosis, and 1 patient was latent tuberculosis infection. All cases were affected unilaterally. Six patients had solitary granuloma and 1 patient had multiple granuloma. Fundus examination showed 7 eyes with subretinal yellow-white lesions and exudative retinal detachment. Five eyes presented with retinal hemorrhage. Baseline visual acuity ranged from hand motion to 0.5. In FFA,2 eyes demonstrated hypofluorescence in the early stage and hyperfluorescence in the late stage,while 5 eyes revealed hyperfluorescence in the early stage and fluorescence leakage in the late stage. Needle-like high fluorescein spots were found in the margins of the lesions in 4 cases. ICGA revealed hypofluorescentce in the early phase and hyperfluorescence with obscure boundary in the late phase. After standard anti-tuberculosis treatment(the course of treatment was 6 to 18 months),inflammation was controlled at the end of follow-up in all cases. Conclusion Choroidal tuberculoma can associate with active or inactive pulmonary tuberculosis, or latent tuberculosis infection. The main presentations of choroidal tuberculoma are subretinal yellow-white lesions at the posterior pole, and exudative retinal detachment. Standard anti-tuberculosis treatment can improve ocular inflammation. (Ophthalmol CHN, 2019, 28: 336-340)

    Clinical features of 39 patients with presumed tubercular retinal vasculitis
    CAO Xu-sheng, LI Qian, HU Feng, PENG Xiao-yan
    2019, 28(5):  341-344.  doi:10. 13281/j. cnki. issn.1004-4469. 2019. 05. 005
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    Objective To investigate the clinical features of presumed tubercular retinal vasculitis. Design Retrospective case series. Participants 39 consecutive patients (72 eyes) with presumed tubercular retinal vasculitis who consulted at the ophthalmic clinic of Beijing Tongren Hospital from June 2013 to June 2019. Methods We retrospectively reviewed the clinical features of the above-mentioned 39 patients (72 eyes). Main Outcome Measures Age, sex, systemic tuberculosis history, causes of visual impairment, laterality, the features of color fundus photography, fundus fluorescein angiography (FFA) and optical coherence tomography (OCT). Results Mean age of the enrolled patients was 32.3±12.3 years. The patients were predominantly male (n=33/39; 84.6%). 7 patients (17.9%) had known history of systemic tuberculosis. A total of 33 patients (84.6%) had bilateral involvement. 29 patients (38 eyes) consulted at the clinic because of vitreous hemorrhage, 4 patients (5 eyes) of them had underwent pars plana vitrectomy and/or silicon oil injection. Among the 62 eyes which can be distinguished by color fundus photography and FFA, 54 eyes (87.1%) had occlusive type retinal vasculitis and/ or retinal neovascularization, 22 eyes (35.5%) had macular edema, 15 eyes (24.2%) had active or healed focal choroiditis lesions, 9 eyes (14.5%) had secondary branch retinal venous occlusion. Conclusions Male, bilateral involvement, vitreous hemorrhage, occlusive retinal vasculitis and/ or secondary retinal neovascularization, macular edema, focal choroiditis lesions, and secondary branch retinal venous occlusion are common clinical features of presumed tubercular retinal vasculitis. (Ophthalmol CHN, 2019, 28: 341-344)

    Comparison of the efficacy of multi-point and single-point laser in the treatment of diabetic retinopathy
    XIE Tian-hua, BAO Xin, SUN Chao, ZHUANG Miao, TAN Cheng-ye, YAO Yong
    2019, 28(5):  345-349.  doi:10. 13281/j. cnki. issn.1004-4469. 2019. 05. 006
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    Objective To compare the effects of multi-point scanning laser and traditional single-point krypton laser in the treatment of diabetic retinopathy (DR). Design Case-control study. Participants A total of 117patients (220 eyes) with clinically diagnosed DR from January 2013 to June 2015. Methods Patients were randomly divided into two groups including the experimental group (58patients, 112 eyes) and the control group (59 patients,108 eyes).The experimental group received pan-retinal photocoagulation (PRP) with multi-point scanning laser, and the control group received PRP with single-point krypton laser. Fundus fluorescein angiography (FFA) was performed 3 months after laser therapy. On the day after laser treatment, we scored the pain according to the Numerical Rating Scale (NRS), recorded the energy index of laser therapy, and calculated the energy density. Best-corrected visual acuity (BCVA), central macular thickness (CMT), mean deviation of perimetry were measured at 1, 3 and 6 months after laser therapy. Main Outcome Measures BCVA, CMT and mean deviation of perimetry before and after treatment, the pain score on the day of laser therapy, the laser energy and laser energy density. Results The laser time in the experimental group (39.07±5.10 min) was shorter than that in the control group (52.36±7.47 min) (t=5.63, P<0.01). The laser energy density of the experimental group (68.23±12.16 mw*ms/μm2) were lower than those of the control group (157.64±31.63 mw*ms/μm2)(t=7.75,P<0.01). The pain score after laser treatment in the experimental group (1.46±0.633) was significantly lower than that in the control group (2.43± 0.95) (t=6.61, P<0.01). There were 30 eyes (26.78%) with improved visual acuity in the experimental group, compared to 32 eyes (29.62%) in the control group (χ2=1.85, P=0.39). Compare to the pre-treatment measurement, the average BCVA were both improved in the two groups (2.43± 0.95 vs. 2.70±2.62) (t=0.27, P=0.82), but the reduction of MCT was significantly (t=-1.02, P=0.03) smaller in experimental group (27.66±46.87 μm) than in the control group (34.47±51.77 μm). The reduction of average threshold sensitivity was significantly smaller (t=9.55, P<0.01) in experimental group (1.22±0.50 dB) than in control group (2.32±1.10 dB). The vitreous hemorrhage rate of experimental group 2.67% (3/112) was similar to that of control group (1.85% (2/118), χ2=0.17, P=0.68). There were 28 eyes (25%) in the experimental group received supplemental laser therapy compared to 20 eyes (18.51%) in the control group(χ2=1.35, P=0.24). Conclusions Multi-point scanning laser achieves the same therapeutic outcomes as the single-point mode with relatively minor functional damage. (Ophthalmol CHN, 2019, 28: 345-349)

    Analysis of impact factors of visual acuity 1 year after vitrectomy for idiopathic macular hole
    LIU Yu-yan1, WANG Hong-yan2, PENG Su-fen3, WANG Ying1, XIAO Bo1, HAN Quan-hong1
    2019, 28(5):  350-353.  doi:10. 13281/j. cnki. issn.1004-4469. 2019. 05. 007
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    Objective To study the 1-year postoperative visual acuity of idiopathic macular hole treated with 25G vitrectomy and its associated factors. Design Retrospective case series. Participants One hundred and three eyes of 100 idiopathic macular hole patients treated in Tianjin Eye Hospital from December 2015 to February 2017 were included. All the patients were treated with 25G vitrectomy combined with internal limiting membrane peeling or flap and followed for 1+ years. Patients who failed follow-up were excluded. Method Age, gender and course duration and axial length measured with IOL master were recorded preoperatively. The best-corrected visual acuity(BCVA) and coherent optical tomography(OCT) were performed before operation and at one-year follow-up. The patients were divided into group A and group B according to the postoperative visual acuity ≤ 0.3 or > 0.3 respectively, or group C and group D according to the vision increase after operation ≤ 0.6 or >0.6 respectively. The factors affecting postoperative visual acuity and visual acuity increase were analyzed. Main Outcome Measures Age, course of duration, AL, BCVA and macular hole diameter. Results There was statistically significant difference in preoperative visual acuity and minimum linear diameter of hole between group A and group B (both P<0.001), while there was no significant difference between the two groups in age, gender, axial length, refraction, duration of disease, and the stage (all P>0.05). There was statistically significant difference in preoperative visual acuity between group C and group D (P<0.001), but no significant difference in age, sex, axial length, refraction, duration of disease, minimum linear diameter of hole and the stage (all P>0.05). Conclusion The worse the visual acuity before surgery, the more the visual acuity increase after surgery. With the increase of the minimum linear diameter of macular hole, the postoperative visual acuity gets worse. But the postoperative visual acuity increasement was not related to minimum linear diameter of hole. (Ophthalmol CHN, 2019, 28: 350-353)

    Analysis of misdiagnosed and missed diagnosis of familial exudative vitreoretinopathy
    ZHANG Jing1, DENG Guang-da2, ZHAO Qi2, LU Hai2
    2019, 28(5):  354-358.  doi:10. 13281/j. cnki. issn.1004-4469. 2019. 05. 008
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    Objective To summarize the characteristics of clinically missed or misdiagnosed patients with familial exudative vitreoretinopathy (FEVR). Design A retrospective case analysis. Participants 28 cases with FEVR (55 eyes) presented to Beijing Tongren Hospital from February 2017 to August 2018 who had been misdiagnosed previously and 25 families of these cases (50 persons including father and mother). Methods We summarized the symptoms, the ocular characteristics and the examination results of these patients. The causes of misdiagnosis were analyzed, and the characteristics of the family history of these cases were summarized. Main Outcome Measures Clinical symptoms, signs under slit-lamp microscope and funduscopy, fundus fluorescence angiography (FFA) and color Doppler ultrasound. The data of the parents' FFA and the family history. Results Of the 28 FEVR patients in this study, 1 patient was involved unilaterally and the others were involved bilaterally. 20 cases (71.43%) had bilateral asymmetric disease stage. 18 cases presented (64.29%) with strabismus. 35 eyes (63.64%) had leopard-like fundus, and 30 eyes (54.54%) had cataract. The fundus and FFA in FEVR are characteristic. Each stage of FEVR can be misdiagnosed and missed. Some common misdiagnosed diseases in early childhood were as following: congenital cataract (2 cases), persistent hyperplastic primary vitreous (14 cases), glaucoma(3 cases), strabismus(4 cases). The common missed diseases in teenagers included high myopia and amblyopia(4 cases) and rhegmatogenous retinal detachment(3 cases). A total of 25 families were examined with FFA, in which father or mother were positive in 12 families, with a positive rate of 12/25 (48%). Conclusion FEVR with various forms of presentation can be easily misdiagnosed. The children and teenagers with cataract, anomalies of vitreous, glaucoma, strabismus should be considered the possibility of FEVR, even without a FEVR family history. (Ophthalmol CHN, 2019, 28: 354-358)

    Characteristics of outer retinal structure in cone dystrophy based ERG
    LIU Ke-gao, BAI Feng-ge, CHEN Chang-xi, ZHANG Zheng, PENG Xiao-yan
    2019, 28(5):  359-363.  doi:10. 13281/j. cnki. issn.1004-4469. 2019. 05. 009
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    Objective To investigate the characteristics of outer retinal structure and retinal function in patients with cone dystrophy (COD). Design Retrospective case series. Participants 12 (24 eyes) COD and 20 (40 eyes) normal controls were retrospectively analyzed. Methods Full-field flash electroretinogram (ERG) was used to examine the function of retinal cone and rod system. Outer retinal structure was examined by optical coherence tomography(OCT). COD was divided into two categories based on the results of ERG. Category 1: The function of cone responses decreased remarkably while the function of rod system was normal. Category 2: The function of cone responses decreased remarkably and the function of rod system decreased slightly. Main Outcome Measures Morphological changes of the outer retinal structure, central macular thickness (CMT), The amplitude of rod b-wave under dark adaptation, cone response a-wave and 30 Hz flicker response under light adaptation. Results Category 1: there was no obvious difference compared to normal controls in the appearance of fundus images and the outer retinal structure. Category 2: macular reflex diffused or disappeared on color fundus images. The outer limited membrane, ellipsoid zone and interdigitation zone blurred or disappeared, but the RPE/Bruch`s complex was intact. The CMT of Category 2 COD (213.42±12.10 μm) was significantly thinner than that of normal (253.56±3.98 μm) and category 1 COD (248.25±8.79 μm) (P<0.0001, P=0.03 respectively). Conclusion Clinical diagnosis of Category 1 COD relies on ERG, since the outer retinal structure shows almost normal. On the contrary, Category 2 COD not only shows abnormal function of cones, but also shows abnormal outer retinal structure. (Ophthalmol CHN, 2019, 28: 359-363)

    Spontaneous peripapillary subretinal hemorrhage in 18 children
    GUO Yin1, LIU Li-juan2, LV Yan-yun1, TANG Ping1, WU Min1, FENG Yi1
    2019, 28(5):  364-367.  doi:10. 13281/j. cnki. issn.1004-4469. 2019. 05. 010
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    Objective To summarize the clinical characteristics of spontaneous peripapillary subretinal hemorrhage (PSH) in 18 children. Design Retrospective case series. Participants 18 patients (18 eyes) with peripapillary subretinal hemorrhage from Tongren Eye Care Center from July to August 2017 were included. The age of the participants ranged from 9~16 years (mean 12.8±1.9 years). 11 cases were boys (61.1%) and 7 cases were girls (38.9%). Methods We reviewed the clinical data including the refractive error, visual acuity and color fundus examination, and some parameters of optic disc were measured. Main Outcome Measures The location, the morphology of the hemorrhage and optic disc. Results All the participants were myopic. Mean spherical equivalent (SE) was -3.42±1.54 D (range: -6.25 D~-0.63 D) in PSH eyes, and -3.57±1.93 D (range: -8.00D~0.00 D) in fellow eyes (P=0.39). All children had isolated, monocular, nasal or inferionasal peripapillary subretinal hemorrhage, a crowded-tilted optic disc and parapapillary atrophy. Optic ovality was 1.43±0.19 in PSH eyes, and 1.38±0.22 in fellow eyes which was not significantly different, but higher than the control group (1.23±0.08, P<0.01). Conclusion We summarized the clinical characteristics of peripapillary subretinal hemorrhages in children. All the patients were myopic and the hemorrhages primarily occured at nasal and appeared oval shape. PSH patients have the typical fundus characteristic of myopia, such as tilted optic disc and elevated nasal edge. (Ophthalmol CHN, 2019, 28: 364-367)

    Analysis of short-term refractive status changes after strabismus surgery and its influence factors
    ZHAO Bo-wen, FU Jing, ZHOU Jin-qiong, QI Meng, WANG Jing-hui, SUN Xing-li
    2019, 28(5):  368-371.  doi:10. 13281/j. cnki. issn.1004-4469. 2019. 05. 011
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    Objective To investigate changes in best corrected visual acuity (BCVA) and refractive status short-term after strabismus surgery. Design Prospective clinical study. Participants 321 cases (475 eyes) were collected from December 16, 2013 to August 31, 2017 in Beijing Tongren hospital with a mean ageof 12.2±15.1 years (range 3-58). Methods All surgery eyes were divided into five groups: Group 1 had one rectus recession; Group 2 had one rectus recession combined with rectus resection on the antagonistic muscle; Group 3 had one rectus recession combined with improved rectus linear tucking on the antagonistic muscle; Group 4 had one rectus recession combined with one oblique recession and Group 5 had two rectus combined with one oblique recession. Main Outcome Measures The BCVA and refractive status before surgery and 1 months after surgery (Patients under 12 years old were done under ciliary muscle paralysis). Results There were no significant differences in preoperative BCVA, spherical equivalent (SE), or astigmatism among the five groups (P=0.75, 0.56, 0.39). There were no significant differences in BCVA among the five groups at one months(P=0.29). There were no significant differences in BCVA before and 1month after surgery. There were no significant differences in SE before and 1month after surgery in group 1-4. In group 5, SE significantly decreased after surgery, from -0.67±2.34 D to -1.09±1.16 D. Before surgery astigmatism in group 1 was 0.52±0.83 D, in group 2 was 0.74±0.52 D, in group 3 was 0.73±1.19 D, in group 4 was 0.61±1.67 D, in group 5 was 0.71±1.41 D. 1 month after surgery astigmatism in group 1 was 0.81±0.88 D, in group 2 was 1.12±1.55 D, in group 3 was 1.14±2.30 D, in group 4 was 1.06±1.69 D and in group 5 was 1.39±2.05 D, The astigmatism increased at one months in all groups compared to preoperative levels (all P<0.01). Conclusion The strabismus surgery increases astigmatism in early stage. Increased number of operated muscles may lead to more spherical equivalent and astigmatism diopter change. (Ophthalmol CHN, 2019, 28: 368-371)

    Myocilin Asn 450 Tyr promotes the expression of extracellular matrix protein in human primary trabecular meshwork cells and the significance
    YAN Xue-jing, WU Shen, LIU Qian, ZHANG Jing-xue
    2019, 28(5):  374-380.  doi:10. 13281/j. cnki. issn.1004-4469. 2019. 05. 012
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    Objective To investigate the effects of Myocilin point mutation(c.A1348T: p.N450Y, Myoc-N450Y) on the expression of extracellular matrix (ECM) protein in human primary trabecular meshwork cells (HTMC) , so as to explore the mechanism of Myoc-N450Y causing glaucoma. Design Experimental study. Participants Human primary trabecular meshwork cells. Methods The experiment was divided into three groups: nine samples in total, empty vector group (Empty), wild type myoc (Myoc-WT) group and Myoc-N450Y group. Lentivirus mediated overexpression method was used to overexpress Myoc-WT gene or Myoc-N450Y gene in HTMC. Western Blot and qRT-PCR were used to quantify the expression of ECM protein collagenⅠ (COL Ⅰ), collagen Ⅳ (COL Ⅳ), fibronectin (FN) and matrix metalloproteinase (MMP) related gene matrix metalloproteinase 2 (Mmp2), matrix metalloproteinase 9 (Mmp9) in Myoc-WT or Myoc-N450Y group. Lentiviral vectors of Myoc-WT and Myoc-N450Y were constructed. Lentivirus expressing Myoc-WT or Myoc-N450Y was packaged and the multiplicity of infection (MOI) of HTMC was determined. HTMC was infected by Myoc-WT lentivirus particles or Myoc-N450Y lentivirus particles. Western Blot and qRT-PCR were used to detect the overexpression of Myoc gene and the effect of N450Y mutation on the expression of Col Ⅰ, Col Ⅳ, Fn, Mmp2 and Mmp9. Main Outcome Measures The expression of Col Ⅰ, Col Ⅳ, Fn, Mmp2 and Mmp9. Results The results of double enzyme digestion and sequencing showed that lentivirus vectors overexpressing Myoc-WT or Myoc-N450Y was successfully constructed, and the MOI in HTMC was 5. Western Blot and qRT-PCR results showed that protein level and mRNA level of Myoc gene were highly over-expressed in Myoc-WT and Myoc-N450Y groups. The relative expression level of Myoc gene in Empty group, Myoc-WT group and Myoc-N450Y group was 1.00±0.02, 28.88±1.28, 22.06±0.47 (F=1020.02,P<0.001). The relative mRNA expression level of Col Ⅰ, Col Ⅳ and Fn in Myoc-N450Y group was 2.08±0.07, 1.76±0.08,2.63±0.06, significantly higher than that of Myoc-WT group (0.93±0.04, 0.95±0.09, 0.89±0.06) (all P<0.001). Compared to the expression in Myoc-WT group, the protein level of COL Ⅰ and FN were significantly upregulated in Myoc-N450Y group. The relative mRNA levels of Mmp2 and Mmp9 in Myoc-N450Y group were 0.32±0.02 and 0.33±0.15, which was significantly lower than that of Myoc-WT group (1.01±0.03 and 0.95±0.03) (all P<0.001). Conclusion Lentiviruses overexpressing Myoc gene in HTMC were successfully prepared, and it was proved that overexpression of Myoc-N450Y promoted the expression of Col Ⅰ, Col Ⅳ, Fn and inhibit the expression of Mmp2 and Mmp9 in HTMC. Therefore, we speculate that Myoc-N450Y may be involved in the occurrence and development of glaucoma by regulating the expression of ECM protein-related genes. (Ophthalmol CHN, 2019, 28: 374-380)

    Presumed ocular histoplasmosis syndrome
    2019, 28(5):  386-391.  doi:10.13281/j.cnki.issn.1004-4469.2019.05.016
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    More and more ophthalmologists pay much attention to presumed ocular histoplasmosis syndrome (POHS), as with the graduallyin-depth understanding of outer retinal diseases. However, most eye doctors keep wondering the syndrome for the exotic disease is rare in China. In this article, the relationships among POHS, histoplasma and histoplasmosis are elucidated firstly, then the pathogenesis, clinical manifestations, differential diagnosis and treatments of POHS are summarized systematically. (Ophthalmol CHN, 2019, 28: 386-391)