Niederecker C, Sauter B, Fürnsinn A M, Rappersberger K
Abteilung für Allgemeine Dermatologie, Universitätsklinik für Dermatologie, Wien.
Hautarzt. 1996 Sep;47(9):711-5. doi: 10.1007/s001050050495.
We report a patient who developed malignant transformation of a cellular blue nevus. At the age of 19 years the congenital, pigmented tumor on the left buttock was histopathologically diagnosed as cellular blue nevus. Thirty years later the tumor dramatically increased in size, involving the entire left buttock within several months. Multiple biopsies revealed the presence of a cellular blue nevus within the papillary dermis and an invasive, pleomorphic pigmented sarcoma in the depth of the tissue spreading into subcutis and skeletal muscle. Both benign and malignant cells were S100+, vimentin+ and HMB-45+, but only the malignant tumor cells stained positive for the proliferating cell nuclear antigen. General examination disclosed multiple metastases in the paraaortal lymph nodes and the retroperitoneum as well as a single brain metastasis. Despite palliative therapy with ionizing radiation and chemotherapy, the patient developed generalized metastases and died within weeks. This case clearly confirms that cellular blue nevi have the potential for malignant transformation and that the malignant variant may behave aggressively just as a malignant melanoma.
我们报告了一例细胞性蓝痣发生恶性转化的患者。19岁时,左侧臀部的先天性色素性肿瘤经组织病理学诊断为细胞性蓝痣。30年后,肿瘤大小急剧增加,在几个月内累及整个左侧臀部。多次活检显示,乳头真皮内存在细胞性蓝痣,组织深部有浸润性、多形性色素性肉瘤,蔓延至皮下组织和骨骼肌。良性和恶性细胞均为S100+、波形蛋白+和HMB-45+,但只有恶性肿瘤细胞增殖细胞核抗原染色呈阳性。全身检查发现主动脉旁淋巴结和腹膜后有多处转移,以及单发脑转移。尽管采用了电离辐射和化疗的姑息治疗,患者仍发生全身转移并在数周内死亡。该病例明确证实细胞性蓝痣有恶性转化的可能,且恶性变体的行为可能与恶性黑色素瘤一样具有侵袭性。