GMS ophthalmology cases最新文献

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Adie's pupil and systemic manifestations: a rare unilateral presentation. 爱迪氏瞳孔及全身表现:罕见的单侧表现。
GMS ophthalmology cases Pub Date : 2024-12-03 eCollection Date: 2024-01-01 DOI: 10.3205/oc000246
M N Vimisha, M Shah Virna, Kumar Karthik, R Sharanya
{"title":"Adie's pupil and systemic manifestations: a rare unilateral presentation.","authors":"M N Vimisha, M Shah Virna, Kumar Karthik, R Sharanya","doi":"10.3205/oc000246","DOIUrl":"10.3205/oc000246","url":null,"abstract":"<p><p>We present a case of a young woman who presented with blurring of vision in her right eye, worsening on near work. Detailed ophthalmic and neurological evaluation was done, which revealed light near dissociation, vermiform iris movements, constriction to diluted pilocarpine with absent deep tendon reflexes. Laboratory investigation indicated mild iron deficiency anemia and reduced vitamin D3 level. On orthopedic evaluation she was diagnosed with right knee joint arthritis and grade 1 patellar chondromalacia. Neuroimaging was within normal limits. Magnetic resonance imaging (MRI) pelvis and lumbar spine showed left ovarian cyst, small periurethral cyst and small hemagioma in left sacral ala. A diagnosis of Holmes-Adie syndrome was made and she was prescribed photochromatic glasses.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"14 ","pages":"Doc14"},"PeriodicalIF":0.0,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11730439/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142985588","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Transient anterior chamber intraocular lens opacification by triamcinolone acetonide following intravitreal injection. 玻璃体注射曲安奈德致短暂性前房人工晶状体混浊。
GMS ophthalmology cases Pub Date : 2024-12-03 eCollection Date: 2024-01-01 DOI: 10.3205/oc000248
Kshitiz Kumar, Deepak Agarwal, Aditya Bajaj, Subrata Saha
{"title":"Transient anterior chamber intraocular lens opacification by triamcinolone acetonide following intravitreal injection.","authors":"Kshitiz Kumar, Deepak Agarwal, Aditya Bajaj, Subrata Saha","doi":"10.3205/oc000248","DOIUrl":"10.3205/oc000248","url":null,"abstract":"<p><strong>Background: </strong>Pseudophakic cystoid macular edema (CME) following primary anterior-chamber intraocular lens (ACIOL) implantations is commonly seen. Intravitreal triamcinolone acetonide (IVTA) injections have shown significant improvement in visual acuity and retinal thickness in refractory pseudophakic CME. Pseudohypopyon following IVTA injection is a known entity.</p><p><strong>Objective: </strong>To report a rare complication of transient acute vision loss due to ACIOL coating with triamcinolone acetonide particles following intravitreal injection.</p><p><strong>Methods: </strong>Case study.</p><p><strong>Results: </strong>A patient developed pseudophakic cystoid macular edema two months post complicated cataract operation with ACIOL implantation. Despite topical steroid treatment, CME persisted and the patient was administered intravitreal triamcinolone acetonide injection. Acute vision loss due to dense coating of ACIOL with triamcinolone particles was noted on the next day. Conservative management led to spontaneous clearing of intraocular lens (IOL) and resolution of CME in 4 weeks.</p><p><strong>Conclusions: </strong>Opacification of ACIOL following IVTA injection is a rare complication which can be seen in eyes with compromised zonular/capsular bag integrity.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"14 ","pages":"Doc16"},"PeriodicalIF":0.0,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11730686/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142985602","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Radius-Maumenee syndrome (idiopathic dilated episcleral vessels). Radius-Maumenee综合征(特发性外膜血管扩张)。
GMS ophthalmology cases Pub Date : 2024-12-03 eCollection Date: 2024-01-01 DOI: 10.3205/oc000247
Carolina Tagliari Estacia, Aluisio Rosa Gameiro Filho, Izadora Bouzeid Estacia da Silveira, Martina Estacia Da Cas, Rodrigo Rosa Gameiro
{"title":"Radius-Maumenee syndrome (idiopathic dilated episcleral vessels).","authors":"Carolina Tagliari Estacia, Aluisio Rosa Gameiro Filho, Izadora Bouzeid Estacia da Silveira, Martina Estacia Da Cas, Rodrigo Rosa Gameiro","doi":"10.3205/oc000247","DOIUrl":"10.3205/oc000247","url":null,"abstract":"<p><strong>Purpose: </strong>Idiopathic elevated episcleral venous pressure (IEEVP) or Radius-Maumenee syndrome (RMS) is a rare disease without any identified underlying cause. An increasing episcleral venous pressure (EVP) leads to raised intraocular pressure (IOP) and consequently glaucomatous damage of the optic nerve. The objective of this paper is to report this rare condition as well as its clinical management.</p><p><strong>Observations: </strong>During cataract evaluation a 38-year-old female patient referred to redness in her right eye that had started more than 3 years before. The IOP was 22 mmHg in her right eye and 14 mmHg in her left eye, although she was already using Timolol drops. Biomicroscopy revealed diffusely engorged episcleral vessels, without any other relevant findings. Intracranial magnetic resonance imaging (MRI) was normal. For that reason, the diagnosis of RMS was established. After 3 months, the patient remains in use of Timolol and Latanoprost eye drops, with intraocular pressure within normal levels. She continues to be followed up on a regular outpatient basis.</p><p><strong>Conclusions and significance: </strong>RMS is a diagnosis of exclusion, based on clinical findings and imaging exams. Treatment includes eyes drops and surgery in refractory cases.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"14 ","pages":"Doc15"},"PeriodicalIF":0.0,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11730685/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142985599","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cancer-associated retinopathy secondary to gallbladder carcinoma. 继发于胆囊癌的癌症相关视网膜病变。
GMS ophthalmology cases Pub Date : 2024-09-23 eCollection Date: 2024-01-01 DOI: 10.3205/oc000243
Karel Goyvaerts, Tanja Coeckelbergh, Pieter-Paul Schauwvlieghe, Michel van Lint
{"title":"Cancer-associated retinopathy secondary to gallbladder carcinoma.","authors":"Karel Goyvaerts, Tanja Coeckelbergh, Pieter-Paul Schauwvlieghe, Michel van Lint","doi":"10.3205/oc000243","DOIUrl":"10.3205/oc000243","url":null,"abstract":"<p><strong>Objective: </strong>To present a rare case of cancer-associated retinopathy secondary to gallbladder carcinoma.</p><p><strong>Methods: </strong>Retrospective case report. Drugs used in case report: methylprednisolone (Medrol), CAS number: 83-43-2, producer: Pfizer; carboplatin, CAS number: 41575-94-4, producer: Accor; etoposide, CAS number: 33419-42-0, producer: Teva; methotrexate (Ledertrexate), CAS number: 59-05-2, producer: Pfizer.</p><p><strong>Results: </strong>A 57-year-old Moroccan man was referred with bilateral progressive vision loss in the last 4 months. At presentation, best corrected visual acuity (BCVA) was counting fingers for the right eye and 20/500 for the left eye. Examination demonstrated signs of vitritis, an electronegative full-field electroretinography (FF-ERG), ocular coherence tomography (OCT) abnormalities and multiple hyperautofluorescent round lesions on fundus autofluorescence imaging (FAF). The diagnosis of cancer-associated retinopathy (CAR) was considered, thus a positron emission tomography-computed tomography (PET-CT) was performed and revealed the presence of a metastasized gallbladder carcinoma. Additional fluorescence in situ hybridization (FISH) showed seropositivity for anti-retinal autoantibodies. High-dose corticosteroids together with anti-tumoral medication (carboplatin-etoposide) gradually improved the BCVA to 20/66 for the right eye and 20/20 for the left eye.</p><p><strong>Conclusions: </strong>Consider the diagnosis of CAR in patients with progressive concentric visual field loss, uveitis and fundus abnormalities, especially if bilateral. If CAR is suspected, perform a full work-up: FF-ERG, OCT, and whole-body PET-CT. In the treatment of CAR, immunosuppressives are mostly used, combined with antitumoral therapy. However, in the long-term, progressive visual loss is expected in most cases.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"14 ","pages":"Doc11"},"PeriodicalIF":0.0,"publicationDate":"2024-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11462702/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142395693","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Epithelial downgrowth masquerading as granulomatous anterior and intermediate uveitis with histopathologic evidence of 5-FU treatment. 伪装成肉芽肿性前葡萄膜炎和中葡萄膜炎的上皮细胞增生,组织病理学证据显示曾接受过 5-FU 治疗。
GMS ophthalmology cases Pub Date : 2024-09-23 eCollection Date: 2024-01-01 DOI: 10.3205/oc000245
Colin P Froines, Alexander D Lin, Kaivon Pakzad-Vaezi, Gordana Juric-Sekhar, Caitlin S Latimer, Kathryn P Scherpelz, C Dirk Keene, Eissa M Hanna, Michael R Banitt, Luis F Gonzalez-Cuyar
{"title":"Epithelial downgrowth masquerading as granulomatous anterior and intermediate uveitis with histopathologic evidence of 5-FU treatment.","authors":"Colin P Froines, Alexander D Lin, Kaivon Pakzad-Vaezi, Gordana Juric-Sekhar, Caitlin S Latimer, Kathryn P Scherpelz, C Dirk Keene, Eissa M Hanna, Michael R Banitt, Luis F Gonzalez-Cuyar","doi":"10.3205/oc000245","DOIUrl":"10.3205/oc000245","url":null,"abstract":"<p><strong>Purpose: </strong>Highlight an unusual case of epithelial downgrowth (EDG) masquerading as granulomatous anterior and intermediate uveitis with histopathologic evidence of 5-fluorouracil (5-FU) treatment.</p><p><strong>Case description: </strong>A 33-year-old man presented after multiple corneal surgeries and neodymium-doped yttrium aluminum garnet (Nd:YAG) capsulotomies with subacute angle closure, pain, light sensitivity, and decreased vision. Exam was notable for granulomatous keratic precipitates, an opacified lens capsule, and vitreous cell/haze. An anterior chamber paracentesis was sent for 16 s (pan-bacterial) and 28 s (pan-fungal) rRNA polymerase chain reaction testing, which returned negative. Diagnostic argon laser photocoagulation was performed on the iris and lens capsule, which blanched upon laser photocoagulation, and subsequent iris biopsy confirmed the presence of epithelial downgrowth (EDG). The patient was treated with multiple injections of 5-FU with repeat biopsy demonstrating both a reduction and apparent resolution in epithelial cell burden after 5-FU.</p><p><strong>Conclusion: </strong>This case demonstrates an unusual presentation of EDG in a young patient with granulomatous anterior and intermediate uveitis, where simple office-based procedures of Argon laser photocoagulation and anterior chamber paracentesis helped aid in diagnosis and management. Histopathological examination in serial specimens demonstrated the effect of 5-FU on EGD. To our knowledge, this case is the first to describe histopathological reduction in epithelial cell burden with sustained resolution.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"14 ","pages":"Doc13"},"PeriodicalIF":0.0,"publicationDate":"2024-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11462678/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142395725","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pseudophakic corneal edema caused by Descemet membrane detachment using high-resolution swept-source OCT imaging. 利用高分辨率扫描源 OCT 成像,观察由 Descemet 膜脱落引起的假性角膜水肿。
GMS ophthalmology cases Pub Date : 2024-09-23 eCollection Date: 2024-01-01 DOI: 10.3205/oc000244
Maximilian K Köppe, Ramin Khoramnia, Gerd U Auffarth, Victor A Augustin
{"title":"Pseudophakic corneal edema caused by Descemet membrane detachment using high-resolution swept-source OCT imaging.","authors":"Maximilian K Köppe, Ramin Khoramnia, Gerd U Auffarth, Victor A Augustin","doi":"10.3205/oc000244","DOIUrl":"10.3205/oc000244","url":null,"abstract":"<p><strong>Background: </strong>Small Descemet membrane detachments after cataract surgery are relatively common and most cases do not require any secondary surgical intervention and can be treated conservatively. However, in case of advanced Descemet membrane detachment (DMD), it needs to be recognized and treated appropriately. The advent of anterior segment imaging using optical coherence tomography (OCT) technology has made diagnosing pathologies of the anterior segment accurate and time efficient and has proven as an invaluable tool to guide decision making.</p><p><strong>Case presentation: </strong>A 71-year-old patient presented after complicated cataract surgery with decreased visual acuity and cloudy vision. On examination, best corrected visual acuity was 1.5 logMAR. A high-resolution swept-source OCT (Anterion, Heidelberg Engineering, Heidelberg, Germany) was used to better evaluate and visualize the extent of DMD. An anterior chamber gas bubble was injected to reattach the Descemet membrane (DM) to the corneal stroma. The success of the surgery was visualized using the high-resolution swept-source OCT. This revealed a completely attached Descemet membrane.</p><p><strong>Conclusions: </strong>Clinically, it can be difficult to distinguish the etiology of epithelial and stromal edema post cataract surgery. This case demonstrated the clinical usefulness using high resolution swept source imaging to guide clinical decision making in evaluating timing and treatment success of pneumodescemetopexy after complicated cataract surgery.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"14 ","pages":"Doc12"},"PeriodicalIF":0.0,"publicationDate":"2024-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11462704/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142395726","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Diffuse preretinal infiltrates in a patient with orbital atypical T-cell lymphoproliferative infiltration masquerading posterior uveitis. 一名伪装成后葡萄膜炎的眼眶非典型 T 细胞淋巴增生性浸润患者的弥漫性视网膜前浸润。
GMS ophthalmology cases Pub Date : 2024-09-23 eCollection Date: 2024-01-01 DOI: 10.3205/oc000242
Bilge Batu Oto, Oğuzhan Kılıçarslan, Didar Uçar, Samira Hagverdiyeva, Ahmet Murat Sarıcı
{"title":"Diffuse preretinal infiltrates in a patient with orbital atypical T-cell lymphoproliferative infiltration masquerading posterior uveitis.","authors":"Bilge Batu Oto, Oğuzhan Kılıçarslan, Didar Uçar, Samira Hagverdiyeva, Ahmet Murat Sarıcı","doi":"10.3205/oc000242","DOIUrl":"10.3205/oc000242","url":null,"abstract":"<p><strong>Purpose: </strong>To report an aggressive and rapidly progressive case of atypical T-cell lymphoproliferative infiltration both with intraocular and orbital involvement and preretinal infiltrates.</p><p><strong>Methods: </strong>Medical records and imaging of the patient were retrospectively reviewed.</p><p><strong>Case presentation: </strong>A 25-year-old woman presented first with preretinal infiltrates resembling uveitis and developed orbital and intracranial signs eventually during her evaluation. Clinical presentation worsened gradually. The patient developed bilateral proptosis, pupillary dilation and uvula deviation. Diagnostic orbital incision biopsy revealed T-cell lymphoproliferative disease.</p><p><strong>Conclusion: </strong>This case gives evidence that intraocular involvement due to T-cell lymphoproliferative disease may present as a masquerade syndrome and should be kept in mind in patients with extraordinary presentation.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"14 ","pages":"Doc10"},"PeriodicalIF":0.0,"publicationDate":"2024-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11462703/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142395694","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Combined use of intravitreal bevacizumab and oral steroid treatment in three diabetic papillopathy patients: a diagnostic and treatment challenge. 在三名糖尿病乳头状瘤病患者中联合使用玻璃体内贝伐单抗和口服类固醇治疗:诊断和治疗难题。
GMS ophthalmology cases Pub Date : 2024-06-25 eCollection Date: 2024-01-01 DOI: 10.3205/oc000238
Burcu Taşkıran Kandeğer, Mehmet Argun, Levent Tök, Özlem Tök
{"title":"Combined use of intravitreal bevacizumab and oral steroid treatment in three diabetic papillopathy patients: a diagnostic and treatment challenge.","authors":"Burcu Taşkıran Kandeğer, Mehmet Argun, Levent Tök, Özlem Tök","doi":"10.3205/oc000238","DOIUrl":"10.3205/oc000238","url":null,"abstract":"<p><p>Diabetic papillopathy (DP), a form of optic disc edema, is characterized by decreased visual acuity and mild to severe visual field defects. While there is no consensus about treatment, some publications report that intravitreal anti-vascular endothelial growth factor (anti-VEGF) injection may be beneficial. To our knowledge, however, no research reports on the effects of combining anti-VEGF injection and oral steroids in DP treatment. In this case report we present three DP cases that showed rapid improvement following therapy with intravitreal bevacizumab and oral steroids. Optic disc edemas were significantly decreased, and visual acuities were markedly increased in the first week of treatment. This report suggests that combined use of these therapies may be safely used in patients diagnosed with DP.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"14 ","pages":"Doc06"},"PeriodicalIF":0.0,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11238643/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141592280","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Unilateral alacrimia as a presenting symptom of Meckel's cave tumour. 作为梅克尔洞穴瘤首发症状的单侧白细胞增多症。
GMS ophthalmology cases Pub Date : 2024-06-25 eCollection Date: 2024-01-01 DOI: 10.3205/oc000241
Ignacio Manuel López Miñarro, Laura Prieto Domínguez, Víctor Manuel Asensio-Sánchez
{"title":"Unilateral alacrimia as a presenting symptom of Meckel's cave tumour.","authors":"Ignacio Manuel López Miñarro, Laura Prieto Domínguez, Víctor Manuel Asensio-Sánchez","doi":"10.3205/oc000241","DOIUrl":"10.3205/oc000241","url":null,"abstract":"<p><p>Meckel's cave tumour, a rare benign tumour originating from the Schwann cells surrounding the trigeminal nerve within the Meckel's cave region, can present with a variety of clinical manifestations. We report a case of a 44-year-old male patient who presented with symptoms of tear deficiency, including dryness, ocular discomfort, and blurred vision. Diagnostic evaluation revealed the presence of a Meckel's cave tumour harming the trigeminal nerve, leading to alacrimia. This case highlights the association between Meckel's cave tumour and tear deficiency disorders.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"14 ","pages":"Doc09"},"PeriodicalIF":0.0,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11238642/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141592291","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A case of endogenous endophthalmitis caused by Escherichia coli septicemia. 一例由大肠杆菌败血症引起的内源性眼底病。
GMS ophthalmology cases Pub Date : 2024-06-25 eCollection Date: 2024-01-01 DOI: 10.3205/oc000239
Tejinder Talwar, Prateek Chandra, Sugandha Goel, Kuntal Patel
{"title":"A case of endogenous endophthalmitis caused by Escherichia coli septicemia.","authors":"Tejinder Talwar, Prateek Chandra, Sugandha Goel, Kuntal Patel","doi":"10.3205/oc000239","DOIUrl":"10.3205/oc000239","url":null,"abstract":"<p><p>Endogenous endophthalmitis is a severe sight-threatening condition that requires urgent intervention. It is a rare complication of <i>Escherichia coli</i> septicemia. We herein report a case of left eye endogenous endophthalmitis with uncontrolled type 2 diabetes mellitus with pyelonephritis associated with <i>Escherichia coli</i> septicemia. Vitrectomy was done along with intravitreal antibiotics and steroids. There was significant improvement in vision after vitrectomy.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"14 ","pages":"Doc07"},"PeriodicalIF":0.0,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11238644/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141592637","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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