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骨髓纤维化相关淋巴增殖性疾病:16例回顾性研究及文献复习

Myelofibrosis-associated lymphoproliferative disease: retrospective study of 16 cases and literature review.

作者信息

Etienne A, Gruson B, Chatelain D, Garidi R, Royer B, Sevestre H, Marolleau J P, Damaj G

机构信息

Department of Clinical Hematology, Centre Hospitalier Universitaire, University Hospital of Amiens, 1 Place Victor Pauchet, 80000 Amiens, France.

出版信息

Adv Hematol. 2009;2009:179847. doi: 10.1155/2009/179847. Epub 2009 Nov 25.

Abstract

Background. To better describe the clinical, biological, and the outcome of non-Hodgkin's lymphoma (NHL) with, at the initial presentation, bone marrow fibrosis (MF). Patients and Methods. From January 2001 to January 2007, 16 eligible patients with NHL and MF were retrieved from the Pathology Department of the University hospital of Amiens. Median age of patients was 62 years (range 16-74) with a sex ratio male/female of 3. Results. MF is associated with all types of lymphoma predominantly with B-cell phenotype and it seems to be more associated with low-grade NHL. B-symptoms are more frequent at diagnosis and more patients presented with an elevated LDH level. JAK-2 was negative in the 10 patients analysed. Two patients presented with features of primary MF with no evidence of lymphoma. Overall response rate was 94% after the first line of therapy with regression or improvement of MF. Relapse occurred in 8 patients (47%) with recurrence of MF in all of them. After a median follow-up of 42 months, 12 patients were alive with an overall survival rate for the entire group of 75%. Conclusions. MF-associated NHL is a rare manifestation which may be associated with all types of NHL and its presence does not seem to confer a poor prognosis. A search for lymphoproliferation should be considered when the cause of MF is not apparent.

摘要

背景。为了更好地描述初诊时伴有骨髓纤维化(MF)的非霍奇金淋巴瘤(NHL)的临床、生物学特征及预后。患者与方法。2001年1月至2007年1月,从亚眠大学医院病理科检索出16例符合条件的NHL合并MF患者。患者中位年龄为62岁(范围16 - 74岁),男女比例为3。结果。MF与所有类型的淋巴瘤相关,主要为B细胞表型,似乎与低度NHL的相关性更强。B症状在诊断时更常见,更多患者乳酸脱氢酶(LDH)水平升高。在分析的10例患者中JAK - 2为阴性。2例患者表现为原发性MF特征,无淋巴瘤证据。一线治疗后总体缓解率为94%,MF消退或改善。8例患者(47%)复发,均出现MF复发。中位随访42个月后,12例患者存活,全组总生存率为75%。结论。MF相关的NHL是一种罕见表现,可能与所有类型的NHL相关,其存在似乎并不预示预后不良。当MF病因不明时,应考虑排查淋巴增殖性疾病。

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