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子宫血管周上皮样细胞瘤放化疗后继发急性淋巴细胞白血病

Acute lymphoblastic leukemia secondary to chemoradiotherapy for perivascular epithelioid cell tumor of uterus.

作者信息

Jeon In-sang, Yi Dae Yong

机构信息

Department of Pediatrics, Gil Medical Center, Gachon Medical School, Gachon University of Medicine and Science, Incheon 405-760, Korea.

出版信息

Pediatr Hematol Oncol. 2009 Mar;26(2):85-8. doi: 10.1080/08880010902754859.

Abstract

Acute lymphoblastic leukemia (ALL), a primary hematologic malignancy that is especially common in childhood, occurs relatively rarely as a secondary malignant neoplasm. Available data indicate that ALL often follows chemoradiotherapy for soft tissue sarcoma. Perivascular epithelioid tumor (PEComa), a primitive mesenchymal tissue origin, can be classified as a soft tissue sarcoma. An 11-year-old girl was diagnosed with ALL secondary to chemoradiotherapy (vincristine, ifosfamide, and anthracycline) and radiotherapy comprising 45 Gy to the whole pelvis for PEComa. ALL, FAB L2, and immunophenotypically pro-B developed 16 months after the final chemotherapy treatment. Moreover, a cytogenetic study of lymphoblasts showed t(1;11)(p32;q23). Herein, the authors report a case of secondary ALL that might be related to a previously used intercalating DNA topoisomerase II inhibitor (anthracycline) for a very rare sarcoma, PEComa.

摘要

急性淋巴细胞白血病(ALL)是一种原发性血液系统恶性肿瘤,在儿童中尤为常见,作为继发性恶性肿瘤相对少见。现有数据表明,ALL常继发于软组织肉瘤的放化疗之后。血管周上皮样细胞瘤(PEComa)起源于原始间叶组织,可归类为软组织肉瘤。一名11岁女孩被诊断为放化疗(长春新碱、异环磷酰胺和蒽环类药物)及针对PEComa的全盆腔45 Gy放疗后继发的ALL。ALL,FAB L2型,免疫表型为前B细胞型,在最后一次化疗后16个月出现。此外,对淋巴母细胞的细胞遗传学研究显示t(1;11)(p32;q23)。在此,作者报告一例继发性ALL病例,可能与之前用于一种非常罕见的肉瘤——PEComa的嵌入性DNA拓扑异构酶II抑制剂(蒽环类药物)有关。

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