Shields Carol L, Eagle Ralph C, Ip Michael S, Marr Brian P, Shields Jerry A
Ocular Oncology Service, Wills Eye Hospital, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.
Retina. 2006 Jul-Aug;26(6):684-7. doi: 10.1097/01.iae.0000236485.24808.f2.
To describe a case of two uveal melanomas in a child with mild ocular melanocytosis.
A 6-year-old girl was followed for 5 years with an ill-defined, slowly enlarging presumed choroidal nevus in the postequatorial fundus. Ocular oncology evaluation revealed mild sectorial scleral and uveal melanocytosis and an episcleral sentinel vessel superotemporally. Two discrete uveal melanomas were present. In the circumpapillary and macular region, tumor 1 was diffuse at 9.0 mm in base and 4.1 mm in thickness and with overlying subretinal fluid. In the ciliary body, tumor 2 was discovered by transillumination and was 6.0 mm in base and 2.2 mm in thickness. Enucleation was performed.
Histopathologic analysis disclosed two discrete uveal melanomas in a bed of diffuse mild uveal melanocytosis. Tumor 1 was a mixed, predominantly epithelioid cell melanoma with active mitotic figures, and tumor 2 was a mixed, predominantly spindle cell melanoma. The choroid between the melanomas showed only benign, dendritic melanocytes consistent with melanocytosis. There was no extrascleral extension.
Ocular melanocytosis can predispose to one or multiple uveal melanomas. Lifetime ophthalmic monitoring of affected patients is warranted.
描述一名患有轻度眼部黑素沉着症的儿童发生两例葡萄膜黑色素瘤的病例。
一名6岁女孩因赤道后眼底有边界不清、缓慢增大的疑似脉络膜痣而接受了5年的随访。眼部肿瘤学评估显示有轻度扇形巩膜和葡萄膜黑素沉着,颞上象限有一条巩膜前哨血管。存在两例独立的葡萄膜黑色素瘤。在视乳头周围和黄斑区,肿瘤1呈弥漫性,基底9.0 mm,厚度4.1 mm,伴有视网膜下液。在睫状体,通过透照法发现肿瘤2,基底6.0 mm,厚度2.2 mm。遂行眼球摘除术。
组织病理学分析显示在弥漫性轻度葡萄膜黑素沉着的背景中有两例独立的葡萄膜黑色素瘤。肿瘤1是混合型,主要为上皮样细胞黑色素瘤,有活跃的有丝分裂象,肿瘤2是混合型,主要为梭形细胞黑色素瘤。黑色素瘤之间的脉络膜仅显示与黑素沉着症一致的良性树突状黑素细胞。无巩膜外扩展。
眼部黑素沉着症可诱发一例或多例葡萄膜黑色素瘤。有必要对受影响的患者进行终身眼科监测。