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组织细胞肉瘤合并急性淋巴细胞白血病:一种罕见的关联——病例报告及文献综述

Histiocytic sarcoma with acute lymphoblastic leukemia a rare association: case report and literature review.

作者信息

Ganapule Abhijeet P, Gupta Mayank, Kokil Gautami, Viswabandya Auro

机构信息

Department of Haematology, Christian Medical College and Hospital, Ida Scudder Road, Vellore, 632004 Tamil Nadu India.

Department of Pathology, Christian Medical College and Hospital, Ida Scudder Road, Vellore, 632004 Tamil Nadu India.

出版信息

Indian J Hematol Blood Transfus. 2014 Sep;30(Suppl 1):305-8. doi: 10.1007/s12288-014-0375-3. Epub 2014 Apr 4.

Abstract

Definition and diagnostic criteria for histiocytic sarcoma (HS) have changed over last two decades due to available new immunohistochemical markers, as well as better understanding of the biology of disease. We report here a case of 4 years old boy diagnosed as acute lymphoblastic leukemia (ALL), who later developed HS of pleura, when he was on maintenance phase of ALL protocol. HS constitutes less than 1 % of the haematolymphoid neoplasm, even more rare is association of HS with ALL. Thus reporting here a rare association of HS with ALL, will help in knowing the actual incidence of HS as well as association with ALL.

摘要

由于有了新的免疫组织化学标志物以及对疾病生物学有了更好的理解,组织细胞肉瘤(HS)的定义和诊断标准在过去二十年中发生了变化。我们在此报告一例4岁男孩,他最初被诊断为急性淋巴细胞白血病(ALL),在ALL方案维持期时后来发展为胸膜HS。HS在血液淋巴系统肿瘤中占比不到1%,HS与ALL的关联更为罕见。因此,在此报告HS与ALL的罕见关联,将有助于了解HS的实际发病率以及与ALL的关联情况。

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本文引用的文献

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Histiocytic sarcoma : an updated literature review based on the 2008 WHO classification.
J Clin Exp Hematop. 2013;53(1):1-8. doi: 10.3960/jslrt.53.1.
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Clinicopathologic features of histiocytic lesions following ALL, with a review of the literature.
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Histiocytic sarcoma after acute lymphoblastic leukaemia: a common clonal origin.
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