A Case with Idiopathic Bilateral Multifocal Retinal Pigment Epithelium Detachment

Göz polikliniğine yakını görememe şikayeti ile başvuran 47 yaşındaki bayan hastanın yapılan oftalmolojik muayenesinde en iyi düzeltilmiş görme keskinliği sağ gözde: 10/10, sol gözde 10/10' idi. Hastanın göz içi basınçları sırasıyla sağ:14 mmhg, sol: 16 mmhg 'idi. Biyomikroskobik muayenede her iki göz ön segment muayeneleri doğal görünümdeydi. Hastanın dilate fundus muayenesinde her iki foveada kistik ve yüzeyden hafif kabarık hipopigmente değişiklikler olduğu gözlendi. Hastanın metamorfopsi şikayeti yoktu. Aynı zamanda hastanın yapılan serolojik testlerinde herhangi bir patoloji saptanmadı. Sistemik herhangi bir problemi olmayan hastaya yapılan flöresein anjiografi (FA) ve optik kohorens tomografi (OCT) tetkikleri sonucunda, İdyopatik retina pigment epitel dekolmanı tanısı konuldu

Bilateral İdyopatik Multifokal Retina Pigment Epitel Dekolmanlı Bir Olgu

A 47-year-old woman presented with near sight issues with 10/10 best corrected visual acuity in both eyes. The intraoculer pressure was 14mmhg in right eye and 16mmhg in left eye. The slit-lamp examination showed a normal anterior chamber. The dilated fundus examination showed that there were cystic, hypopigmented, and swollen lessions in the both fovea. The patient did not have metamorphopsia. At the same time in serological tests performed on the patient did not develop any pathology. With no present systemic problem, the patient was diagnosed with idiopathic retina pigment epitel detachment at the end of examination with fluorecein anjiography and optical chorence tomography

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