Busam Klaus J, Wolchok Jedd, Jungbluth Achim A, Chapman Paul
Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
J Cutan Pathol. 2004 Mar;31(3):274-80. doi: 10.1111/j.0303-6987.2003.00154.x.
Diffuse melanosis is a rare event associated with advanced metastatic malignant melanoma. A 35-year-old woman with stage IV melanoma is presented, who developed slate bluish-gray to brown discoloration of her skin after chemotherapy-induced tumor lysis syndrome. A number of studies were performed to re-evaluate possible mechanisms of melanosis. Skin tissue was examined on routine hematoxylin-and-eosin-stained sections, Fontana stains, immunohistochemical studies with antibodies for Melan-A, gp100, tyrosinase, FXIIIa, and CD68, and by electron microscopy. The main cell types found to contain melanin pigment were histiocytes and dendritic cells. In the dermis, they were distributed mainly around venules. In the subcutaneous fat, they were scattered throughout the fat lobule. Melanin pigment was not only seen within cells but also extracellularly. No melanoma cells were seen in the skin. No increase in melanin pigment or number of melanocytes was seen in the epidermis. A bone marrow biopsy contained melanophages but no melanoma cells. Ultrastructural examination of the patient's serum revealed the presence of melanosomes. Sequence analysis of the tumor's cDNA failed to identify any mutations in the tyrosinase gene, and no tyrosinase protein was detected in non-melanocytic cells, indicating that it was unlikely that a mutation had resulted in a secretory form of the protein. These findings document that diffuse melanosis may result from tumor lysis, with release of melanosomes into the bloodstream.
弥漫性黑变病是一种与晚期转移性恶性黑色素瘤相关的罕见病症。本文报告了一名35岁的IV期黑色素瘤女性患者,她在化疗诱导的肿瘤溶解综合征后出现了皮肤从石板蓝灰色变为棕色的色素沉着。进行了多项研究以重新评估黑变病可能的机制。对皮肤组织进行了常规苏木精-伊红染色切片、Fontana染色、使用针对Melan-A、gp100、酪氨酸酶、FXIIIa和CD68的抗体进行免疫组织化学研究,并通过电子显微镜检查。发现含有黑色素的主要细胞类型是组织细胞和树突状细胞。在真皮中,它们主要分布在小静脉周围。在皮下脂肪中,它们散布在整个脂肪小叶中。黑色素不仅可见于细胞内,也可见于细胞外。皮肤中未见黑色素瘤细胞。表皮中黑色素或黑素细胞数量未见增加。骨髓活检发现有噬黑素细胞,但未见黑色素瘤细胞。对患者血清的超微结构检查发现了黑素小体的存在。对肿瘤cDNA的序列分析未能鉴定出酪氨酸酶基因的任何突变,并且在非黑素细胞中未检测到酪氨酸酶蛋白,这表明不太可能是突变导致了该蛋白的分泌形式。这些发现证明弥漫性黑变病可能是由肿瘤溶解导致黑素小体释放到血液中引起的。