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两例分别发生在套细胞淋巴瘤和妊娠滋养细胞疾病之后的治疗相关性急性早幼粒细胞白血病(t-APL)。

Two cases of therapy-related acute promyelocytic leukemia (t-APL) after mantle cell lymphoma and gestational trophoblastic disease.

作者信息

Au W Y, Ma S K, Chung L P, Chim C S, Kwong Y L

机构信息

University Department of Medicine, Professorial Block, Queen Mary Hospital, Pokfulam Road, Hong Kong.

出版信息

Ann Hematol. 2002 Nov;81(11):659-61. doi: 10.1007/s00277-002-0552-6. Epub 2002 Nov 6.

Abstract

We report two cases of secondary acute promyelocytic leukemia (APL). One patient presented with concurrent APL and missed abortion 1 year after etoposide-based chemotherapy for gestational trophoblastic disease. A prolonged complete remission was achieved with standard chemotherapy. An elderly man developed APL 1 year after alkylator-based chemotherapy for mantle cell lymphoma (MCL). A complete clinical and molecular remission was obtained with chemotherapy and all- trans retinoic acid, followed by arsenic consolidation. Concomitant molecular relapse of APL and MCL clones was detected at 1 year, both of which responded to oral arsenic therapy. High-dose epipodophyllin is a dose risk for secondary APL, but alkylating agents may also be implicated. For patients with a history of active malignancy and heavy previous chemotherapy exposure, the use of nontoxic arsenic therapy appeared to be effective and prudent.

摘要

我们报告了两例继发性急性早幼粒细胞白血病(APL)。一例患者在接受依托泊苷为基础的化疗治疗妊娠滋养细胞疾病1年后,并发APL并稽留流产。采用标准化疗实现了长期完全缓解。一名老年男性在接受烷化剂为基础的化疗治疗套细胞淋巴瘤(MCL)1年后发生APL。化疗联合全反式维甲酸治疗后获得完全临床和分子缓解,随后进行砷剂巩固治疗。1年后检测到APL和MCL克隆同时分子复发,二者均对口服砷剂治疗有反应。高剂量表鬼臼毒素是继发性APL的剂量风险因素,但烷化剂也可能与之有关。对于有活动性恶性肿瘤病史且既往接受过大量化疗的患者,使用无毒的砷剂治疗似乎有效且谨慎。

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