bilateral bullous idiopathic central serous chorioretinopathy

نویسندگان

محمدرسول صبوری

mr sabouri amiralomonin hospital, guilan university of medical sciences, guilan, iranرشت- خیابان 17 شهریور- مجتمع آموزشی درمانی امیرالمومنین (ع)

چکیده

purpose: to present a case of bilateral idiopathic central serous chorioretinopthy (icsc) complicated by bullous serous retinal detachment (rd). case report: a 26-year old female suffered from acute loss of vision in the both eyes. best spectacle-corrected visual acuity was 1/10 ou. the examination of anterior segment was unremarkable and a mild vitreous reaction was noted. dilated fundus examination revealed bullous exudative retinal detachment in both eyes. fundus fluorescein angiography (ffa) demonstrated multiple hyperfluorescent spots at the level of retinal pigment epithelium. the initial diagnosis harada's disease (vkh) and oral corticosteroid was started which led to worsening of the condition. therefore, systemic corticosteroid was discontinued and indocyanine green angiography (icg) and ocular coherent tomography (oct) were performed. icg showed extensive choriodopathy and oct showed multiple sensory retinal detachments. on the basis of the abovementioned findings, bullous variant of icsc was diagnosed and the patient was followed up periodically. the lesion resolved spontaneously and completely within 4 months. conclusion: a severe variant of icsc characterized by multiple posterior exudation and bullous rd may affect otherwise a healthy young female. recognition of this atypical presentation is important to avoid inappropriate treatment.

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