Dutton J J, Anderson R L, Schelper R L, Purcell J J, Tse D T
Ophthalmology. 1984 May;91(5):497-507. doi: 10.1016/s0161-6420(84)34261-0.
Oculodermal melanocytosis is a congenital melanoblastic hamartoma affecting ocular tissues and facial skin. It is seen more commonly in oriental and black patients. Malignant degeneration, once believed to be rare in this syndrome, occurs in 4.6% of all reported cases, and is more frequent in whites. The actual incidence of malignant melanoma in this syndrome is difficult to determine as many uncomplicated cases go unreported. The most common site of malignant melanoma associated with this entity is in the choroid. Four previously described orbital tumors represent the second most frequent area of presentation. A review of the literature in this disease is discussed as well as a new case of orbital malignant melanoma associated with it. A second case of presumed orbital melanoma associated with oculodermal melanocytosis is also discussed.
眼皮肤黑素细胞增多症是一种先天性黑素母细胞错构瘤,累及眼部组织和面部皮肤。在东方人和黑人患者中更为常见。恶性变曾被认为在该综合征中罕见,在所有报告病例中发生率为4.6%,在白人中更常见。由于许多无并发症的病例未报告,该综合征中恶性黑色素瘤的实际发病率难以确定。与该实体相关的恶性黑色素瘤最常见的部位是脉络膜。先前描述的四种眼眶肿瘤是第二常见的表现部位。本文讨论了该疾病的文献综述以及与之相关的眼眶恶性黑色素瘤新病例。还讨论了第二例推测与眼皮肤黑素细胞增多症相关的眼眶黑色素瘤病例。