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急性淋巴细胞白血病终末期转变为恶性组织细胞增多症。1例病例报告及文献复习

Acute lymphocytic leukaemia terminating in malignant histiocytosis. A case report and literature review.

作者信息

Heaton A, Kahn L B

出版信息

S Afr Med J. 1980 Mar 29;57(13):502-7.

PMID:6929112
Abstract

A 5-year-old Black girl with acute lymphatic leukaemia died after a short illness during which haematological remission was induced with standard chemotherapeutic agents. At autopsy an unexpected finding was involvement of the spleen, lymph nodes, bone marrow and liver by malignant histiocytosis (MH). There was also evidence of residual leukaemia. A review of the literature revealed 11 other cases with a similar association of leukaemia preceding MH; in 8 of these the leukaemia was of the acute lymphatic type, in 2 of the monocytic type and in 1 of an unusual atypical large lymphoid cell type. The clinico-pathological features of these cases are reviewed.

摘要

一名5岁黑人女孩患急性淋巴细胞白血病,经标准化疗药物诱导血液学缓解后,病程短暂,最终死亡。尸检发现意外情况,脾脏、淋巴结、骨髓和肝脏均有恶性组织细胞增生症(MH)累及。也有残留白血病的证据。文献回顾显示,还有11例类似病例,白血病先于MH出现;其中8例为急性淋巴细胞型白血病,2例为单核细胞型,1例为不常见的非典型大淋巴细胞型。本文对这些病例的临床病理特征进行了回顾。

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