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ALK 阴性间变大细胞淋巴瘤白血病复发。

Leukaemic relapse of anaplastic large cell lymphoma, ALK negative.

机构信息

Hematology Oncology, Augusta University, Augusta, Georgia, USA

Jersey City Medical Center, Jersey City, New Jersey, USA.

出版信息

BMJ Case Rep. 2021 Feb 22;14(2):e239213. doi: 10.1136/bcr-2020-239213.

Abstract

Anaplastic large cell lymphoma (ALCL), ALK negative (ALK-) is an aggressive lymphoproliferative disorder of mature T lymphocytes characterised by hallmark cells, CD30 positivity and lacking ALK protein expression. ALCL, ALK- has to be differentiated from peripheral T-cell lymphoma-not otherwise specified and classical Hodgkin's lymphoma. ALK- anaplastic large cell leukaemia should be considered in a patient with a history of ALCL, ALK- presenting with new leukaemia. We report a rare presentation of relapsed ALCL, ALK- with leukaemia after autologous stem cell transplantation in a 57-year-old male. Leukaemia, either as primary presentation or secondary transformation confers worse prognosis in ALCL, ALK- with very few cases reported so far. Emergency resuscitation with leukapheresis and treatment of tumour lysis syndrome along with supportive care should be followed by combination chemotherapy. Brentuximab vedotin and stem cell transplantation are the backbone of treatment for relapsed/refractory disease.

摘要

间变大细胞淋巴瘤(ALK 阴性)(ALCL,ALK-)是一种成熟 T 淋巴细胞的侵袭性淋巴增生性疾病,其特征为具有 hallmark 细胞、CD30 阳性和缺乏 ALK 蛋白表达。ALCL,ALK-需要与外周 T 细胞淋巴瘤-未另作说明和经典霍奇金淋巴瘤相鉴别。在有 ALCL,ALK-病史并出现新的白血病的患者中应考虑 ALK-间变大细胞白血病。我们报告了一例罕见的复发性 ALCL,ALK-在自体干细胞移植后出现白血病的病例,患者为 57 岁男性。白血病无论是作为首发表现还是继发转化,在 ALCL,ALK-中预后较差,迄今为止报道的病例很少。应进行紧急复苏,行白细胞分离术,并治疗肿瘤溶解综合征,同时进行支持性治疗,然后进行联合化疗。Brentuximab vedotin 和干细胞移植是治疗复发性/难治性疾病的基础。

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