scholarly journals A rare case of solitary optic nerve sarcoidosis mimicking an ocular tumor

2019 ◽  
Vol 10 ◽  
pp. 1
Author(s):  
Jacqueline Wesolow ◽  
Asha Ramsakal
Keyword(s):  
2015 ◽  
pp. bcr2015213510
Author(s):  
Rashim Mannan ◽  
Parijat Chandra
Keyword(s):  

2016 ◽  
pp. bcr2016216465
Author(s):  
Nishant Radke ◽  
Charudutt Kalamkar ◽  
Amrita Mukherjee ◽  
Snehal Radke

2020 ◽  
pp. 112067212098438
Author(s):  
Marco Mafrici ◽  
Laura Toscani ◽  
Umberto Lorenzi

Background: Diabetic papillopathy is a complication of diabetes. It presents with edema, uni or bilateral and vascular alteration of the anterior optic nerve. Often this complication is observed in patients with severe diabetic retinopathy, but is rarely observed in isolated form. Some authors believe that diabetic papillitis is a particular form of non-arteritic anterior ischemic optic neuropathy (NAION). But there is important evidence that confers an inflammatory component to diabetic papillopathy. We report in this work a rare case of isolated acute bilateral diabetic papillopathy developed in a diabetic patient after adding the insulin to the oral hypoglycemic therapy. Case presentation: Male patient, 49-years-old, diabetic type 2, with altered glycemia at follow up, with clinical history of HbA1c 8% to 12% in the last 2 years, on oral hypoglycemic therapy for 10 years. He never had a history of diabetic retinopathy. At the last check-up, this patient presented bilateral papillopathy, without reduction of visual acuity bilaterally. The patient reports he added 10 days before the insulin therapy to the oral hypoglycemic therapy, under medical supervision. Hematochemical and serological tests were requested, which excluded the presence of inflammatory and infectious diseases. The brain magnetic resonance imaging (MRI) with gadolinium excluded the hypothesis of optic neuritis or intracranial hypertension. Cardio-circulatory tests were normal. Fluorescein angiographic examinations and optical coherence tomography (oct) confirmed the bilateral edema and the thickening of optic nerve without other retinal damage. Therefore he was diagnosed with bilateral diabetic papillopathy. Then, diabetologists added pump insulin treatment to the oral hypoglycemic therapy. After 2 months, his blood sugar levels and HbA1C improved and papillopathy regressed. Conclusion: We have reported a rare case of bilateral acute diabetic papillopathy associated with the addition of insulin to the oral hypoglycemic therapy. A randomized control study with diabetic patients, would be useful to verify the possible injuries of the optic nerves during the delicate transition to insulin therapy.


Cureus ◽  
2015 ◽  
Author(s):  
Wyatt L Ramey ◽  
Stacy J Arnold ◽  
Alexander Chiu ◽  
Michael Lemole

2019 ◽  
Vol 13 (1) ◽  
Author(s):  
Ruchi Shrestha ◽  
Amin Kumar Shrestha

Abstract Background Ocular cysticercosis is a disease which rarely involves cutaneous skin and the optic nerve. Patients with clinical presentation of subcutaneous nodules and papilledema should always be evaluated for cysticercosis. Case presentation We report a rare case of ocular cysticercosis with multiple disseminated subcutaneous nodules and papilledema in both eyes. A 22-year-old Brahmin man presented with complaints of gradual loss of vision in both eyes and multiple small masses all over his body. On clinical evaluation, multiple subcutaneous nodules were seen on his face, mandibular area, elbow, arm, and abdomen. A fundus evaluation showed bilateral blurred disc margin. The case was managed with steroids and anti-parasitic drugs. Conclusion This case report highlights the importance of ruling out neurocysticercosis in cases with multiple disseminated subcutaneous nodules and papilledema.


2018 ◽  
Vol 5 (2) ◽  
pp. 1-6 ◽  
Author(s):  
Hiroshi Kanno ◽  
Seiki Osano ◽  
Masamichi Shinonaga

Central nervous system hemangioblastomas are generally restricted to the cerebellum, spinal cord, and brainstem. Supratentorial hemangioblastomas are uncommon, and optic nerve hemangioblastomas are extremely rare, with fewer than 25 reports including this case. In this report, we present the case of a 36-year-old woman with von Hippel-Lindau (VHL) disease who presented with progressive diminution of vison in the left eye due to a retrobulbar optic nerve hemangioblastoma. The patient had a history of cerebellar /spinal hemangioblastomas and pancreatic cysts, and her father and brother were patients with VHL disease. Gadolinium enhanced MRI showed intraorbital retrobulbar enhanced mass on the left optic nerve. The optic nerve hemangioblastoma was treated with fractionated stereotactic radiosurgery using Novalis. Eighteen months after the stereotactic radiosurgery, the tumor volume decreased although the patient lost vision. This report presents an extremely rare case of optic nerve hemangioblastoma, which is the first case treated with stereotactic radiosurgery.


2014 ◽  
Vol 62 (6) ◽  
pp. 728 ◽  
Author(s):  
Somen Misra ◽  
Neeta Misra ◽  
Pratik Gogri ◽  
Rajen Mehta

Author(s):  
Rashmi Singh ◽  
Anup Kumar ◽  
Rajanigandha Tudu ◽  
Payal Raina ◽  
Praveer Munda

Abstract Purpose: Optic nerve glioma (OPG) is a rare tumour of children and adolescents. The treatment is challenging as it may jeopardise the visual outcome. We are reporting a case of bilateral OPG, treated with intensity-modulated radiotherapy in our department. Material and Method: An 18-year-old female presented with a gradually deteriorating vision in both eyes. A detailed clinical and ophthalmological examination was carried out. Her MRI of orbit and brain were suggestive of bilateral optic nerve glioma. She was treated with intensity-modulated radiotherapy to a total dose of 54Gy in 30 fractions over 6 weeks. Results: She well tolerated the treatment. Post radiotherapy at 8 weeks, she had stabilization of vision on clinical assessment. Conclusion: Radiotherapy using IMRT can be successfully used to treat OPG, and it checks tumour growth and prevents further deterioration.


Sign in / Sign up

Export Citation Format

Share Document