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Artikel Jurnal
Yoga Causing Vertebrobasilar Ischemia with Neuro-Ophthalmic Presentation: A Case Report
Introduction: We present a case of a woman experiencing blurry vision and dizziness consistent with vertebrobasilar insufficiency (VBI) during yoga, confirmed with dynamic transcranial Doppler ultrasound. This is the first case identifying yoga as a cause of vertebrobasilar ischemia leading to…
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Artikel Jurnal
A Case Report of Presumed West Nile Virus Chorioretinitis in a Non-Endemic Area: Atypical Serology and Imaging Features of Old and New Lesions
Introduction: West Nile virus (WNV) infection is a recognized cause of neuroinvasive disease and chorioretinitis, typically reported in endemic regions and often associated with positive IgM serology. However, atypical presentations with discordant serology can occur, particularly in non-endemic…
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Artikel Jurnal
Acute Retinal Necrosis with Choroidal Inflammation, Optic Perineuritis, and Early Retinal Detachment: A Case Report
Introduction: The aim of the study was to describe a rare presentation of acute retinal necrosis (ARN) in an immunocompetent adult, with choroidal, optic nerve, and orbital inflammation with exudative retinal detachment (ERD), complicated by early rhegmatogenous retinal detachment (RRD). This is a…
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Artikel Jurnal
Hidradenitis Suppurativa Presenting with Ocular Manifestations in a 44-Year-Old Male: A Case Report
Introduction: Οcular manifestations of hidradenitis suppurativa (HS) are uncommon and typically include episcleritis, keratitis, and uveitis. We report a rare case of posterior scleritis and peripheral ulcerative keratitis (PUK) in a patient with HS. Case Presentation: A 44-year-old male with no…
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Artikel Jurnal
A Case of Branch Retinal Arteriole Occlusion and Paracentral Acute Middle Maculopathy after COVID-19 Infection
Introduction: The aim of this study was to report a case of segmental deep capillary plexus ischemic injury after COVID-19 infection in a vaccinated otherwise healthy male. Case Presentation: A healthy 38-year-old male presented with a complaint of not being able to see above his fixation point in…
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Artikel Jurnal
Bromfenac with Sodium Bisulfite Inducing Contact Dermatitis and Corneal Ring Infiltrate: A Case Report
Introduction: The aim of the study was to report a case of bromfenac with sodium bisulfite preservative induced contact dermatitis and a secondary sterile corneal ring infiltrate. Case Presentation: A 44-year-old male presented with a 1-week unilateral periocular dermatitis and eye redness…
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Artikel Jurnal
Presumed Sterile Cluster Endophthalmitis following Intravitreal Triamcinolone Acetonide: A Rare Case Series
Introduction: Presumed sterile endophthalmitis (PSE) is a noninfectious inflammatory reaction that mimics infectious endophthalmitis following intravitreal injections. It is a rare but clinically significant complication of intravitreal triamcinolone acetonide (IVTA). This case report describes the…
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Artikel Jurnal
Laser Iris Depigmentation Resulting in Markedly Elevated Intraocular Pressure and Herpes Simplex Keratitis with Corneal Scarring: Case Report
Introduction: Laser iris depigmentation (LID) is a cosmetic procedure designed to alter eye color by reducing iris pigment using an Nd:YAG laser. While this procedure is increasingly popular, it carries risk of serious, sight-threatening complications. This report highlights two cases that…
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Artikel Jurnal
Presumed Capsular-Bag-Origin Endophthalmitis following Anterior Vitrectomy for Posterior Capsule Opacification in a Patient with Proliferative Diabetic Retinopathy: A Case Report
Introduction: Chronic postoperative endophthalmitis is a rare but serious complication following intraocular surgery. We report a unique case of presumed capsular-bag-origin endophthalmitis that developed after anterior vitrectomy for posterior capsule opacification in a patient with proliferative…
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Artikel Jurnal
Primary Orbital Extranodal NK/T-Cell Lymphoma: A European Case Report
Introduction: Extranodal natural killer/T-cell lymphoma, nasal type (ENKTL), is a rare and aggressive malignancy. Primary orbital involvement is exceptionally uncommon. We report a case of orbital ENKTL in a White patient presenting with rapidly progressive orbital symptoms. Case Presentation: A…
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Artikel Jurnal
Phenotypic Divergence in C19ORF44-Associated Retinal Degeneration despite an Identical Genotype: A Case Report
Introduction: C19ORF44 has recently been identified as a gene associated with autosomal recessive inherited retinal disease (IRD). The function of the gene remains poorly understood, and a previously reported case with identical primary genotype demonstrated a Stargardt-like macular dystrophy…
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Artikel Jurnal
Leber Hereditary Optic Neuropathy in the Elderly: A Case Report
Introduction: Leber hereditary optic neuropathy (LHON) is a mitochondrial disorder typically affecting young males, with rare reports of late-onset disease. Among the three primary LHON mutations, m.14484T>C is generally associated with a relatively favorable visual prognosis. However, the disease…
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Artikel Jurnal
Silicone Oil Migration into the Graft Interface after Descemet Stripping Automated Endothelial Keratoplasty in a Patient with a Past Surgical History of Silicone Oil Tamponade: A Case Report
Introduction: Descemet stripping automated endothelial keratoplasty (DSAEK) is widely accepted as an alternative to penetrating keratoplasty for the treatment of corneal endothelial failure. Surgical outcomes, however, may be compromised in eyes with complex surgical histories, particularly…
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Artikel Jurnal
An Individualized Surgical Approach for the Management of Recurrent Pterygium: A Case Report
Introduction: This case highlights the complexity of managing highly refractory, recurrent pterygium. Despite numerous prior surgeries by experienced anterior segment surgeons, the patient developed persistent fibrosis, symblepharon formation, and functional limitations. This underscores the need…
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Artikel Jurnal
Gasperini Syndrome: A Rare Brainstem Syndrome – A Case Report
Introduction: This unique case demonstrates how subtle ocular motor abnormalities, even in the absence of visual complaints, can lead to the detection of an otherwise clinically silent brainstem lesion. Case Presentation: We report on the incidental discovery of a brain tumor following a traffic…
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Artikel Jurnal
May Acute Appendicitis Complicate the Management of Pseudotumor Cerebri in Shunt-Dependent Patients? A Paediatric Case Report
Introduction: Shunt-dependent secondary pseudotumor cerebri may remain clinically stable for many years; however, intra-abdominal sepsis such as perforated appendicitis can necessitate abrupt shunt removal, eliminating cerebrospinal fluid (CSF) diversion and precipitating sudden, vision-threatening…
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Artikel Jurnal
A Rare Case of Concurrent Carotid Cavernous Fistula and Orbital Cellulitis: Challenging Diagnosis and Divergent Management
Introduction: Carotid cavernous fistula (CCF) is abnormal vascular connections between the cavernous sinus and the carotid artery or its branches, leading to orbital signs. This rare case report illustrates the diagnostic complexities posed by orbital cellulitis and concomitant CCF. Case…
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Artikel Jurnal
Acquired Capillary Hemangioma of the Palpebral Conjunctiva in a Child with Vernal Keratoconjunctivitis: A Case Report and Pathogenetic Hypothesis
Introduction: Acquired capillary hemangioma of the conjunctiva is a rare benign vascular tumor, particularly in the pediatric population and when arising from the palpebral conjunctiva. Its clinical appearance often overlaps with reactive vascular lesions such as pyogenic granuloma, making accurate…
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Artikel Jurnal
Idiopathic Giant Retinal Cyst: A Case Report
Introduction: Idiopathic giant retinal cyst (IGRC) is a rare entity that may mimic a range of retinal or choroidal lesions. Accurate diagnosis and tailored surgical management are essential to achieve anatomical and functional outcomes. Case Presentation: We present the case of a 27-year-old female…
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Artikel Jurnal
Early-Onset Retinal Dystrophy in Alpha-Mannosidosis: A Case Report
Introduction: Alpha-mannosidosis is a rare inherited lysosomal storage disorder characterized by immune deficiency, intellectual disability, hearing loss, and skeletal and facial dysmorphism. It results from biallelic pathogenic variants in MAN2B1 on chromosome 19. Ophthalmic manifestations…
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