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伴有T细胞/组织细胞丰富的B细胞淋巴瘤样区域的结节性淋巴细胞为主型霍奇金淋巴瘤的小肠表现——关于该疾病结外表现的文献综述

Small intestinal presentation of nodular lymphocyte-predominant Hodgkin lymphoma with T cell/histiocyte-rich B cell lymphoma-like areas-with review of literature on extranodal presentation of this disease.

作者信息

Bagwan Izhar N, Knee Graham, Abboudi Zaid, Naresh Kikkeri N

出版信息

J Hematop. 2010 Mar 24;3(1):29-34. doi: 10.1007/s12308-010-0056-6.

Abstract

Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL), accounts for ∼5% of all cases of Hodgkin lymphoma and is characterized by involvement of the peripheral lymph nodes. NLPHL occurs in young adults and is associated with frequent relapses. In 3% to 7% of cases, NLPHL progresses to a diffuse large B cell lymphoma. Furthermore, a proportion of NLPHL also have areas with features of T cell/histiocyte-rich large B cell lymphoma (THRLBCL), either at presentation or on follow-up. Here, we describe a 32-year-old man who presented to the emergency department with small bowel perforation. The resected small bowel showed full-thickness mural ulceration and involvement by a lymphoma with features of NLPHL that also had areas resembling THRLBCL. The patient had axillary lymphadenopathy, biopsy of which showed NLPHL with focal THRLBCL-like areas. Such a lymphoma presenting as small intestinal lesion/perforation has not been reported in the literature before. We take this opportunity to review the literature on extranodal presentations of NLPHL and discuss the natural history of this disease.

摘要

结节性淋巴细胞为主型霍奇金淋巴瘤(NLPHL)占所有霍奇金淋巴瘤病例的约5%,其特征为外周淋巴结受累。NLPHL好发于年轻成年人,且常伴有复发。在3%至7%的病例中,NLPHL会进展为弥漫性大B细胞淋巴瘤。此外,一部分NLPHL在初诊时或随访过程中也会出现具有T细胞/组织细胞丰富的大B细胞淋巴瘤(THRLBCL)特征的区域。在此,我们描述一名32岁男性,因小肠穿孔就诊于急诊科。切除的小肠显示全层壁溃疡,并被具有NLPHL特征且有类似THRLBCL区域的淋巴瘤累及。该患者有腋窝淋巴结肿大,活检显示为NLPHL伴局灶性THRLBCL样区域。此前文献中尚未报道过以小肠病变/穿孔形式出现的此类淋巴瘤。我们借此机会回顾关于NLPHL结外表现的文献,并讨论该疾病的自然史。

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本文引用的文献

1
Biology, clinical course and management of nodular lymphocyte-predominant hodgkin lymphoma.
Hematology Am Soc Hematol Educ Program. 2006:266-72. doi: 10.1182/asheducation-2006.1.266.
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T-cell/histiocyte-rich large B-cell lymphoma: a heterogeneous entity with derivation from germinal center B cells.
Am J Surg Pathol. 2002 Nov;26(11):1458-66. doi: 10.1097/00000478-200211000-00008.
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Primary T-cell-rich B-cell lymphoma masquerading as a meningioma.
Arch Pathol Lab Med. 2000 Nov;124(11):1700-3. doi: 10.5858/2000-124-1700-PTCRBC.
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Primary T-cell-rich B-cell lymphoma of the ethmoid sinus. A case report with 5 years of follow-up.
Arch Pathol Lab Med. 2000 Aug;124(8):1213-6. doi: 10.5858/2000-124-1213-PTCRBC.

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