Fulminant metastatic melanoma complicated by a microangiopathic hemolytic anemia.

N Bhagwati, R Seno, J P Dutcher, L Oleksowicz
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Abstract

A 34-year-old male acutely presented with widely disseminated malignant melanoma, a microangiopathic hemolytic anemia, and disseminated intravascular coagulation. Although the patient had a history of intense childhood exposure to ultraviolet light and an occupational exposure to organic dyes, he had no history of a precursor skin lesion. The histopathology of the patient's bone marrow revealed sheets of malignant cells immunoreactive with S-100, HMB-45, and vimentin and also staining positively for melanin. A bone marrow aspirate revealed myeloid precursors filled with melanin-bearing vacuoles. Immunophenotypic analysis of the patient's bone marrow by flow cytometry revealed a paucity of hematopoietic cells. A karyotypic analysis of the patient's tumor cells demonstrated an abnormal hypertriploid composite clone characterized by multiple numerical and structural abnormalities. Although the patient was treated aggressively with transfusional support, heparin, and chemotherapy, he expired 3 weeks after diagnosis. This is the first recognized case of metastatic melanoma occurring in association with a microangiopathic hemolytic anemia.

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暴发性转移性黑色素瘤合并微血管病溶血性贫血。
34岁男性,急性表现为广泛播散性恶性黑色素瘤,微血管病性溶血性贫血,弥散性血管内凝血。虽然患者有强烈的儿童紫外线照射史和职业性有机染料暴露史,但他没有前驱皮肤病变史。患者骨髓组织病理学显示,恶性细胞对S-100、HMB-45和vimentin有免疫反应,黑色素染色呈阳性。骨髓抽吸显示骨髓前体充满黑色素液泡。流式细胞术对患者骨髓进行免疫表型分析,发现造血细胞缺乏。患者肿瘤细胞的核型分析显示为异常的高三倍体复合克隆,其特征是多个数字和结构异常。尽管患者接受了输血支持、肝素和化疗的积极治疗,但他在确诊后3周死亡。这是第一个公认的转移性黑色素瘤与微血管病溶血性贫血相关的病例。
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