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酷似恶性组织细胞增多症的系统性利什曼病。

Systemic leishmaniasis mimicking malignant histiocytosis.

作者信息

Matzner Y, Behar A, Beeri E, Gunders A E, Hershko C

出版信息

Cancer. 1979 Jan;43(1):398-402. doi: 10.1002/1097-0142(197901)43:1<398::aid-cncr2820430156>3.0.co;2-3.

Abstract

A 22-year-old man with fever, hepato-splenomegaly and severe pancytopenia is described in whom the histologic features of the spleen, liver and lymph nodes were consistent with malignant histiocytosis. Characteristic Leishman-Donovan bodies were demonstrated on a bone marrow aspirate, and the diagnosis of visceral leishmaniasis was confirmed by culturing the flagellated forms of the pathogen, and by an excellent response to sodium stibogluconate. In view of the similarity in clinical and histologic appearance, visceral leishmaniasis must be considered in the differential diagnosis of malignant histiocytosis in geographic areas where leishmaniasis is still endemic.

摘要

本文描述了一名22岁男性,其有发热、肝脾肿大及严重全血细胞减少,脾脏、肝脏和淋巴结的组织学特征符合恶性组织细胞增多症。骨髓穿刺涂片发现了特征性的利杜体,通过培养病原体的鞭毛体形式以及对葡萄糖酸锑钠的良好反应确诊为内脏利什曼病。鉴于临床和组织学表现相似,在利什曼病仍为地方病的地区,内脏利什曼病必须纳入恶性组织细胞增多症的鉴别诊断中。

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