Mandura Rahaf A, Radi Rwan E
Department of Ophthalmology, King Abdulaziz University, Jeddah, SAU.
Department of Ophthalmology, College of Medicine, Umm Al-Qura University, Mecca, SAU.
Cureus. 2021 Mar 22;13(3):e14034. doi: 10.7759/cureus.14034.
Macular coloboma is a rare eye condition that affects around 0.5-0.7/10,000 of live births. Macular coloboma appears as a well-demarcated atrophic lesions that could affect one eye or both eyes on fundus examination. This is a case of a 33-year-old male patient who presented to the outpatient clinic with a history of poor vision in the left eye since childhood. He had a history of strabismus surgery for sensory exotropia (XT) in the left eye. Anterior segment examination of both eyes was normal while the fundus examination of both eyes revealed bilateral chorioretinal lesions in the macula which was larger in the left eye (OS) than the right eye (OD), representing bilateral chorioretinal coloboma. Congenital coloboma is a rare eye condition that leads to non-progressive decrease in visual acuity. Optical coherence tomography (OCT) is the modality of choice in diagnosing and describing macular coloboma.
黄斑缺损是一种罕见的眼部疾病,在每10000例活产中约有0.5 - 0.7例受影响。黄斑缺损表现为界限清晰的萎缩性病变,在眼底检查中可累及一只眼或双眼。这是一名33岁男性患者的病例,他自童年起就有左眼视力差的病史。他有左眼感觉性外斜视(XT)的斜视手术史。双眼眼前节检查正常,而双眼眼底检查显示黄斑区双侧脉络膜视网膜病变,左眼(OS)比右眼(OD)更大,提示双侧脉络膜视网膜缺损。先天性缺损是一种罕见的眼部疾病,会导致视力非进行性下降。光学相干断层扫描(OCT)是诊断和描述黄斑缺损的首选方法。