间变性心脏大细胞淋巴瘤:捷克淋巴瘤研究组(CLSG)数据库中新诊断的非霍奇金淋巴瘤累及心脏的病例报告和分析

C. Lobello, A. Janíková, L. Křen, M. Hermanová, A. Šprláková‐Puková, J. Krejci, Š. Pospíšilová, R. Pytlík, M. Hamouzová, D. Belada, V. Procházka, J. Ďuraš, H. Mociková, M. Trněný
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引用次数: 1

摘要

我们报告一例罕见的间变性大细胞ALK+淋巴瘤(ALCL),最初无症状累及心脏。一位59岁男性右心室壁浸润患者接受了标准的联合化疗(CHOP)并获得缓解,无明显的心脏损害。此外,我们报告了新诊断的非霍奇金淋巴瘤(nhl)中心脏淋巴瘤的实际发病率。在捷克淋巴瘤研究组的数据库中,共发现16例心脏淋巴瘤患者(0.1% nhl)。DLBCL是最常见的组织学亚型(50%),ALCL在12.5%的病例中被确定。初次诊断时,中位年龄为55.5岁(21-74岁),59%为男性。16例累及心脏的患者均无孤立性心脏淋巴瘤。在14/16可评估的患者中,一线治疗的应答率为79%。中位无进展生存期和总生存期几乎相同,约为3.5年(范围;0.05 ~ 16.7岁),中位随访时间为4年。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An anaplastic cardiac large cell lymphoma: A case report and analysis of cardiac involvement in newly diagnosed non-Hodgkin’s lymphoma from the Czech Lymphoma Study Group (CLSG) database
We report a rare case of anaplastic large cell ALK+ lymphoma (ALCL) with initial asymptomatic cardiac involvement. A 59-year-old male with infiltration of the right ventricular wall underwent standard combined chemotherapy (CHOP) and achieved remission without significant cardiac impairment. Additionally, we report the actual incidence of cardiac lymphoma in newly diagnosed non-Hodgkin Lymphomas (NHLs). In total, 16 patients with cardiac lymphoma were found (0.1% NHLs) in the Czech Lymphoma Study Group database. DLBCL was the most frequent histology subtype (50%), and ALCL was identified in 12.5% of cases. At initial diagnosis, the median age was 55.5 (range 21-74) years and 59% were men. None of the 16 patients with cardiac involvement had isolated heart lymphoma. The response to first-line therapy was 79% in 14/16 evaluable patients. The median progression-free survival and overall survival were nearly the same -approximately 3.5 years (range; 0.05-16.7ys), while the median follow up was 4 years.
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