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淋巴结浆细胞瘤。复发性淋巴结病最终发展为伴有多发性神经病和内分泌紊乱的浆细胞发育异常。

Plasmacytoma of lymph node. Recurrent lymphadenopathy terminating in plasma cell dyscrasia with polyneuropathy and endocrine disturbances.

作者信息

Sakuma H, Mori N, Kojima M, Saito T, Tachibana F, Naito M

出版信息

Acta Pathol Jpn. 1984 Sep;34(5):1157-66. doi: 10.1111/j.1440-1827.1984.tb07643.x.

Abstract

A case with lymphadenopathy of the left side of the neck in a 38-year-old male is described. He had a history of several relapses of about 10 years duration. Swollen lymph nodes were histologically similar to those of the hyaline-vascular type of Castleman's disease, but contained clear-cut lymph sinus and a sheet-like proliferation of plasma cells. Lymph follicles showed proliferation and atrophic germinal centers, in which cellular hypertrophy in the wall of ramifying small blood vessels, called angiosclerosis, was frequently encountered. During its progress, the patient developed plasmacytoma of the lymph nodes with varied clinical manifestations such as polyneuropathy, disturbance of gait, unusual perspiration, hirsutism, gynecomastia, bilateral papilledema, and albumino-cytologic dissociation in cerebrospinal fluid.

摘要

本文描述了一名38岁男性左侧颈部淋巴结病的病例。他有大约10年的多次复发史。肿大的淋巴结在组织学上与透明血管型Castleman病相似,但含有清晰的淋巴窦和浆细胞的片状增生。淋巴滤泡显示增生和萎缩的生发中心,其中在分支小血管壁上经常出现细胞肥大,称为血管硬化。在病程中,患者出现了淋巴结浆细胞瘤,伴有多种临床表现,如多发性神经病、步态障碍、异常出汗、多毛症、男性乳房发育、双侧视乳头水肿以及脑脊液中的蛋白细胞分离。

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