Leibowitz M R, Dagliotti M, Smith E, Murray J F
Histopathology. 1980 Sep;4(5):559-66. doi: 10.1111/j.1365-2559.1980.tb02949.x.
A 34-year-old black South African male was treated for lymphangioma-like clinical Kaposi's sarcoma. The disease followed a rapidly fatal course and was characterized by unexplained recurrent pleural effusions and severe refractory anaemia due to the presence of dilated vascular channels in the bone marrow. Definitive diagnosis was only made at autopsy. Lymphangiomatous changes in the skin without spindle cell formation caused diagnostic difficulties.
一名34岁的南非黑人男性因淋巴管瘤样临床型卡波西肉瘤接受治疗。该疾病呈快速致命病程,其特征为不明原因的反复胸腔积液以及因骨髓中存在扩张的血管通道而导致的严重难治性贫血。最终诊断仅在尸检时做出。皮肤中的淋巴管瘤样改变但无梭形细胞形成造成了诊断困难。