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呈现白血病期的弥漫性大B细胞淋巴瘤。

Diffuse large B-cell lymphoma presenting in the leukemic phase.

作者信息

Pires Patricia Puccetti, Kanegae Marcia Yoshie, Rays Jairo, Catania Marcos, Lima Fabiana Roberto, Noronha Thiago Rodrigo, Abdo Andre Neder Ramires, Pereira Juliana

机构信息

Internal Medicine Department - Faculty of Medicine - Universidade de São Paulo, São Paulo/SP - Brazil .

Internal Medicine Division - Hospital Universitário - Universidade de São Paulo, São Paulo/SP - Brazil .

出版信息

Autops Case Rep. 2016 Mar 30;6(1):41-5. doi: 10.4322/acr.2016.027. eCollection 2016 Jan-Mar.

DOI:10.4322/acr.2016.027
PMID:27284540
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4880433/
Abstract

Diffuse large B-cell lymphoma (DLBCL) is the most common non-Hodgkin lymphoma comprising a heterogeneous group of disorders with variable histological and clinical behavior. Although other lymphomas may present in the leukemic phase more frequently, this appearance is unusually observed among DLBCL cases. Diagnosing lymphoma is not always easy, and the patient's clinical status quite often may hamper invasive procedures for diagnosis pushing the clinician to look for alternatives to reach the nearest possible accurate diagnosis. The authors report the case of a middle-aged man who presented the history of malaise, weight loss, and low-grade fever. The peripheral blood count showed leukocytosis with the presence of blasts and thrombocytopenia. The cytological morphology and immunophenotyping of the peripheral blood and bone marrow aspirate, as well as the bone marrow biopsy accompanied by a thorough immunohistochemical analysis, rendered the diagnosis of DLBCL in the leukemic phase. The patient was prescribed R-CHOP with a favorable outcome. Intra-abdominal lymph node biopsy was avoided because of the patient's critical medical condition. The authors highlight this rare form of presentation of DLBCL as well as the combination of peripheral blood, bone marrow aspirate, and bone marrow biopsy for reaching the diagnosis in cases were a lymph node sample is unavailable for the diagnostic work-up.

摘要

弥漫性大B细胞淋巴瘤(DLBCL)是最常见的非霍奇金淋巴瘤,由一组组织学和临床行为各异的异质性疾病组成。尽管其他淋巴瘤可能更频繁地出现在白血病期,但这种表现在DLBCL病例中并不常见。诊断淋巴瘤并不总是容易的,患者的临床状况常常会妨碍进行侵入性诊断程序,促使临床医生寻找替代方法以尽可能准确地进行诊断。作者报告了一例中年男性病例,该患者有全身不适、体重减轻和低热病史。外周血细胞计数显示白细胞增多伴原始细胞出现及血小板减少。外周血和骨髓穿刺液的细胞形态学及免疫表型分析,以及骨髓活检并进行全面的免疫组化分析,确诊为白血病期DLBCL。该患者接受了R-CHOP方案治疗,效果良好。由于患者病情危急,避免了进行腹腔淋巴结活检。作者强调了DLBCL这种罕见的表现形式,以及在无法获取淋巴结样本进行诊断检查的情况下,外周血、骨髓穿刺液和骨髓活检相结合用于诊断的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9642/4880433/5e1770568399/autopsy-06-01041-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9642/4880433/2506acaa2c28/autopsy-06-01041-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9642/4880433/740cccf6b045/autopsy-06-01041-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9642/4880433/5e1770568399/autopsy-06-01041-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9642/4880433/2506acaa2c28/autopsy-06-01041-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9642/4880433/740cccf6b045/autopsy-06-01041-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9642/4880433/5e1770568399/autopsy-06-01041-g03.jpg

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