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窦组织细胞增生伴巨大淋巴结病和结区边缘区淋巴瘤的同时发生。

Concomitant occurrence of sinus histiocytosis with massive lymphadenopathy and nodal marginal zone lymphoma.

机构信息

Department of Pathology, Wake Forest University School of Medicine, Winston-Salem, North Carolina 27157-1072, USA.

出版信息

Arch Pathol Lab Med. 2011 Mar;135(3):390-3. doi: 10.5858/2010-0114-CR.1.

Abstract

Sinus histiocytosis with massive lymphadenopathy (SHML), also known as Rosai-Dorfman disease, is a rare self-limiting disorder of histiocytes with unknown etiology. Sinus histiocytosis with massive lymphadenopathy is most common in children and young adults and is characterized by painless lymphadenopathy. Histologically there is a proliferation of sinus histiocytes with lymphophagocytosis or emperipolesis. On rare occasions, SHML has been associated with lymphoma, usually involving different anatomic sites and developing at different times. We report a case of concomitant SHML and nodal marginal zone lymphoma involving the same lymph node without involvement of other nodal or extranodal sites. The presence of concomitant SHML within the lymph node involved by nodal marginal zone lymphoma may represent the responsiveness of SHML histiocytes to B-cell-derived cytokines in lymphoproliferative disorders. To our knowledge, this is the first description of concomitant occurrence of SHML and nodal marginal zone lymphoma.

摘要

窦组织细胞增生伴巨大淋巴结病(SHML),又称 Rosai-Dorfman 病,是一种病因不明的组织细胞良性增生性疾病,具有自限性。SHML 多见于儿童和青年,以无痛性淋巴结病为特征。组织学上表现为窦组织细胞增生,伴有吞噬现象或噬血细胞现象。在极少数情况下,SHML 与淋巴瘤相关,通常涉及不同的解剖部位,并在不同时间发生。我们报告了一例同时发生的窦组织细胞增生伴边缘区淋巴瘤累及同一淋巴结,而无其他淋巴结或结外部位受累。在边缘区淋巴瘤累及的淋巴结中同时存在窦组织细胞增生可能代表了 SHML 组织细胞对淋巴增生性疾病中 B 细胞来源细胞因子的反应性。据我们所知,这是首例同时发生的窦组织细胞增生伴边缘区淋巴瘤的描述。

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