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Angioimmunoblastic T-cell lymphoma occurring four months after autologous peripheral blood stem cell transplantation with high-dose chemotherapy for follicular lymphoma

机译:自体外周血干细胞移植与滤泡性淋巴瘤大剂量化疗后四个月发生的血管免疫母细胞性T细胞淋巴瘤

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摘要

A 62-year-old Japanese woman was diagnosed as having follicular lymphoma (FL, grade 3, CS IIIA, IPI high-intermediate risk) in May 1998. After eight courses of CHOP therapy, she achieved a complete remission (CR). In November 1998, her FL relapsed, and she achieved a second CR after two courses of MINE therapy. High-dose etoposide was used for autologous peripheral stem cell mobilization. In May 1999, she underwent high-dose chemotherapy with autologous peripheral blood stem cell transplantation (auto-PBSCT). Four months after the auto-PBSCT, bilateral cervical lymphadenopathy developed. Histopathological findings from a biopsied cervical lymph node showed angioimmunoblastic T-cell lymphoma (AILT). The patient was treated with modified CVP therapy, and she is alive with no evidence of lymphoma five years after auto-PBSCT. Clinical and histopathological findings showed that the FL and AILT in this case were not concomitant. It is thought that in this case, the AILT developed as a post-transplant lymphoproliferative disorder after auto-PBSCT for the FL.
机译:1998年5月,一名62岁的日本女性被诊断出患有滤泡性淋巴瘤(FL,3级,CS IIIA,IPI高中级风险)。经过八次CHOP治疗,她完全缓解。 1998年11月,她的FL复发,在进行了两次MINE治疗后,她再次获得了CR。大剂量依托泊苷用于自体外周血干细胞动员。 1999年5月,她接受了自体外周血干细胞移植(auto-PBSCT)的大剂量化疗。自动PBSCT后四个月,双侧颈淋巴结病发展。活检宫颈淋巴结的组织病理学发现显示血管免疫母细胞性T细胞淋巴瘤(AILT)。该患者接受了改良的CVP治疗,并且在自动PBSCT治疗五年后还活着,没有淋巴瘤的迹象。临床和组织病理学结果表明,在这种情况下,FL和AILT不伴有。可以认为,在这种情况下,对于FL,AILT在自体PBSCT后发展为移植后的淋巴增生性疾病。

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