Agrawal P K, Kumar H
Department of Ophthalmology, King George's Medical College, Lucknow.
Indian J Ophthalmol. 1993 Dec;41(4):177-9.
Defects in closure of embryonic fissure and invagination of optic vesicle results in varied clinical presentation of microphthalmos with cyst. In our study, three patients had microphthalmos with cyst in one of their orbits. The cyst presented either as a swelling in the lower lid or as a sinus with purulent discharge associated with absent or small sized eyeball. The microphthalmic eye showed a spectrum of posterior segment abnormalities such as retinal disorganisation, gliosis, choroidal, and scleral coloboma. Microscopically, the cyst connected to the coloboma consisted of an outer layer of fibrovascular tissue and an inner gliotic neuroectodermal layer. The treatment consisted of excision of cyst alone or of microphthalmic eye with cyst. The use of conformers was mandatory after removal of cystic eyeball for near normal development of both orbits to maintain facial symmetry in our paediatric patients.
胚胎裂闭合缺陷和视泡内陷会导致伴有囊肿的小眼畸形出现多种临床表现。在我们的研究中,三名患者其中一个眼眶患有伴有囊肿的小眼畸形。囊肿表现为下睑肿胀或伴有脓性分泌物的窦道,同时伴有眼球缺失或过小。小眼畸形的眼睛表现出一系列后段异常,如视网膜紊乱、胶质增生、脉络膜和巩膜缺损。显微镜下,与缺损相连的囊肿由外层纤维血管组织和内层胶质神经外胚层组成。治疗方法包括单独切除囊肿或切除伴有囊肿的小眼畸形眼球。在切除囊肿性眼球后,必须使用塑形片,以使我们儿科患者的两个眼眶接近正常发育,以维持面部对称。