Utiger C A, Headington J T
Department of Pathology, University of Michigan Medical Center, Ann Arbor.
Arch Dermatol. 1993 Feb;129(2):202-4. doi: 10.1001/archderm.129.2.202.
Noncutaneous psammomatous melanotic schwannoma has recently been reported as an unusual component of Carney's complex (myxomas, spotty pigmentation, and endocrinopathy). The most common locations for this lesion include peripheral nerve roots and the gastrointestinal tract.
A cutaneous psammomatous melanotic schwannoma is reported in a patient with known Carney's complex. This neoplasm was pseudoencapsulated, with epithelioid to spindle-shaped cells and no nuclear atypia. Immunostaining was positive for S100 protein and vimentin, as well for HMB-45 antibody. Electron microscopy showed melanosomes in cytoplasmic processes of cells that were ensheathed by layers of reduplicated basal lamina.
Location in the superficial soft tissues is extremely unusual for psammomatous melanotic schwannomas. Recognition of this new cutaneous marker as a part of this complex may aid in identification of individuals at risk for cardiac myxomas. It is also important that this lesion is not mistaken for melanoma, given the strong HMB-45 positivity.
非皮肤性砂粒体性黑色素性神经鞘瘤最近被报道为卡尼综合征(黏液瘤、斑点状色素沉着和内分泌病)的一种不寻常成分。该病变最常见的部位包括周围神经根和胃肠道。
报道了1例已知患有卡尼综合征的患者发生皮肤砂粒体性黑色素性神经鞘瘤。该肿瘤有假包膜,由上皮样至梭形细胞构成,无核异型性。免疫染色S100蛋白、波形蛋白以及HMB - 45抗体均呈阳性。电子显微镜检查显示,细胞的胞质突起中有黑素小体,周围有多层重复的基底膜包绕。
砂粒体性黑色素性神经鞘瘤位于浅表软组织极为罕见。认识到这种新的皮肤标志物是该综合征的一部分,可能有助于识别有患心脏黏液瘤风险的个体。鉴于HMB - 45强阳性,该病变不被误诊为黑色素瘤也很重要。