Mansour A M, Li H K
Department of Ophthalmology, American University of Beirut, Lebanon.
Ophthalmic Plast Reconstr Surg. 1996 Jun;12(2):104-7. doi: 10.1097/00002341-199606000-00004.
We present a rare case of congenital cystic eye associated with holoprosencephaly and tetralogy of Fallot. The orbital cyst was diagnosed preoperatively by computed tomography (CT) scan, and we present the first magnetic resonance imaging (MRI) finding in such a disorder. The orbital cyst expanded over 7 months of follow-up. The cyst was excised in toto and studied by immunohistochemistry, and its content was analyzed biochemically. The patient achieved an acceptable cosmetic result.
我们报告一例罕见的先天性囊性眼合并全前脑畸形和法洛四联症。眼眶囊肿术前通过计算机断层扫描(CT)诊断,我们展示了这种疾病的首例磁共振成像(MRI)表现。眼眶囊肿在7个月的随访中逐渐增大。囊肿被完整切除并进行免疫组织化学研究,其内容物进行了生化分析。患者获得了可接受的美容效果。