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不确定细胞组织细胞增多症伴随后期发生急性髓细胞白血病。

Indeterminate cell histiocytosis in association with later occurrence of acute myeloblastic leukaemia.

作者信息

Vener C, Soligo D, Berti E, Gianelli U, Servida F, Ceretti E, Caputo R, Passoni E, Lambertenghi Deliliers G

机构信息

Hematology I, Bone Marrow Transplant Unit, Policlinico IRCCS Hospital, Mangiagalli and Regina Elena Foundation, University of Milan, Milan, Italy.

出版信息

Br J Dermatol. 2007 Jun;156(6):1357-61. doi: 10.1111/j.1365-2133.2007.07880.x. Epub 2007 Apr 25.

Abstract

Indeterminate cell histiocytosis (ICH) is a proliferation of indeterminate CD1a+, CD68+, S100+ and CD207- dermal dendritic cells. We describe a 39-year-old man who developed diffuse ICH and, 6 years later, acute myeloblastic leukaemia (AML). He was treated with cyclophosphamide, etoposide and vinblastine until 2003. In August 2004, he presented dyspnoea, hyperpyrexia and infiltration of the lung parenchyma, compatible with an AML invasion, and died after a course of induction chemotherapy. Cytomorphology and immunophenotype analyses suggested an ICH clonal evolution. The leukaemogenic role of etoposide is discussed. ICH has previously been reported in association with B-cell malignancy, but only one case has shown systemic progression.

摘要

未定型细胞组织细胞增多症(ICH)是一种未定型的CD1a +、CD68 +、S100 +和CD207 - 真皮树突状细胞的增殖。我们描述了一名39岁男性,他患上了弥漫性ICH,6年后又患上了急性髓细胞白血病(AML)。他接受了环磷酰胺、依托泊苷和长春碱治疗,直至2003年。2004年8月,他出现呼吸困难、高热和肺实质浸润,符合AML浸润表现,在诱导化疗过程中死亡。细胞形态学和免疫表型分析提示ICH发生了克隆进化。文中讨论了依托泊苷的致白血病作用。ICH此前曾有与B细胞恶性肿瘤相关的报道,但仅有1例出现了全身进展。

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