Kamino H, Tam S T
Department of Dermatology, New York University Medical Center, New York.
Arch Dermatol. 1990 Oct;126(10):1330-3.
We studied six cases of heavily pigmented melanocytic lesions with features of blue nevi within the dermis, but with an additional junctional dendritic component. This compound variant of blue nevus is an uncommon lesion that has not been previously identified as a distinct histologic entity. Immunoperoxidase staining for S100 protein and counterstaining with azure B distinguished the presence of melanocytes among numerous melanophages within the dermis. The compound variant of blue nevus can be distinguished histologically from combined blue nevus, pigmented spindle cell nevus, malignant melanoma, and melanosis due to a regressed malignant melanoma. The six lesions were from three men and three women whose ages ranged from 11 to 51 years (mean, 31 years). Three lesions were located on the trunk, two on the extremities, and one on the head. After a mean follow-up period of 47 months (range, 38 to 58 months), there was no evidence of recurrence.
我们研究了6例真皮内具有蓝痣特征但伴有额外交界性树突状成分的色素沉着严重的黑素细胞性病变。这种蓝痣的复合变体是一种罕见病变,以前未被确认为一种独特的组织学实体。用S100蛋白进行免疫过氧化物酶染色并以天青B复染,可在真皮内众多噬黑素细胞中区分黑素细胞的存在。蓝痣的复合变体在组织学上可与复合性蓝痣、色素性梭形细胞痣、恶性黑素瘤以及消退性恶性黑素瘤所致的黑变病相鉴别。这6例病变来自3名男性和3名女性,年龄范围为11至51岁(平均31岁)。3例病变位于躯干,2例位于四肢,1例位于头部。平均随访47个月(范围38至58个月)后,无复发迹象。