Outer Retinal Microstructure in a Case of Acute Idiopathic Blind Spot Enlargement Syndrome
نویسندگان
چکیده
PURPOSE To present a patient with acute idiopathic blind spot enlargement syndrome who had abnormal changes in the outer retinal microstructure limited to areas with reduced responses on multifocal electroretinograms as well as to the area involving a scotoma. METHODS AND RESULTS We report the case of a 44-year-old man who developed an arcuate scotoma which was associated with a physiological blind spot in the left eye. The ophthalmoscopic, fluorescein angiographic, and full-field electroretinogram findings were normal. The amplitudes of the multifocal electroretinograms were reduced in the area of the scotoma. Optical coherence tomography showed that both the external limiting membrane and the inner and outer segment (IS/OS) line were intact, but that the middle cone outer segment tip line between the IS/OS line and the retinal pigment epithelium was absent in the nasal macular area of the left eye. CONCLUSIONS These findings indicate that the integrity of not only the external limiting membrane and IS/OS line but also the cone outer segment tip line is important for the function of the retina.
منابع مشابه
Recovery of outer retina in acute idiopathic blind spot enlargement (AIBSE)
Purpose To report the anatomic and functional recovery of the ellipsoid zone in a case of acute idiopathic blind spot enlargement (AIBSE), which was documented by serial high-resolution optical coherence tomography imaging. Observations The patient's clinical presentation and follow up visits were documented via Humphrey's Visual Fields, fundus autofluorescence, and high resolution spectral d...
متن کامل[Acute idiopathic blind spot enlargement syndrome associated with choroidal neovascularization].
CLINICAL CASE A 17 year old female consulting due to photopsia and a sudden loss of visual field in left eye (OS), with previous contralateral choroidal neovascularization. The examination suggested an acute idiopathic blind spot syndrome. The progress without treatment was favorable, with a reduction in the scotoma and without a worsening of her visual acuity. DISCUSSION This case report is ...
متن کاملContralateral active ocular toxoplasmosis in Fuchs' heterochromic cyclitis.
1 Jampol LM, Sieving PA, Pugh D, Fishman GA, Gilbert H. Multiple evanescent white dot syndrome: I. Clinical findings. Arch Ophthalmol 1984; 102: 671-4. 2 Sieving PA, Fishman GA, Jampol LM, Pugh D. Multiple evanescent white dot syndrome: II. Electrophysiology of the photoreceptors during retinal pigment epithelial disease. Arch Ophthalmol 1984; 102: 675-9. 3 Dodwell DG, Jampol LM, Rosenberg M, B...
متن کاملAcute, idiopathic blind spot enlargement syndrome.
An otherwise healthy 12-year-old boy was evaluated for an enlarged blind spot in his left eye. Neither optic nerve edema/neuritis nor a retrobulbar mass explained this finding. Consultation with a neuro-ophthalmologist over a period of 14 months resulted in a diagnosis of acute, idiopathic blind spot enlargement syndrome, a rare and poorly understood ocular condition. To the author's knowledge,...
متن کاملAcute Zonal Occult Outer Retinopathy; Revisited
211 Acute zonal occult outer retinopathy (AZOOR) was first described by J. Donald M. Gass in 1992[1] as a “syndrome” characterized by sudden onset photopsia and acute scotomas related to loss of sectors of outer retinal function in typically young, otherwise healthy individuals including 10 female and 3 male subjects.[1] Early funduscopic appearance was often normal; however, most patients deve...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره 2 شماره
صفحات -
تاریخ انتشار 2011