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伴有皮肤受累的结外多中心性Castleman病。

Extranodal multicentric Castleman's disease with cutaneous involvement.

作者信息

Skelton H G, Smith K J

机构信息

Laboratory Corporation of America, Herndon, Virginia, USA.

出版信息

Mod Pathol. 1998 Jan;11(1):93-8.

PMID:9556429
Abstract

Castleman's disease (CAD) is an unusual lymphoid hyperplasia that might be induced by an immunologic reaction to a virus or another infectious organism or drug. CAD commonly occurs in the mediastinal lymph nodes and less frequently in the neck lymph nodes, but other lymph nodes might be involved. Extranodal CAD is rare. We present a 72-year-old woman with diffuse 2- to 5-cm cutaneous nodules that had appeared a few months earlier. The patient underwent a biopsy, and the lesions resolved within 4 months. The patient was asymptomatic except for mild joint pains. Histopathologic findings showed a circumscribed nodule composed of lymphoid follicles with contracted germinal centers and expanded mantle zones. The lymphoid follicles were separated by perivascular bands of sclerotic collagen. Aggregates of epithelioid and dendritic histiocytes were present between follicles, with a prominent lymphoplasmacytic infiltrate and vascular proliferation. Although extranodal CAD has been reported in the skin, we think that this is the first reported case of multicentric cutaneous CAD without evidence of lymph node involvement.

摘要

卡斯特曼病(CAD)是一种罕见的淋巴组织增生,可能由对病毒、其他感染性生物体或药物的免疫反应引起。CAD通常发生在纵隔淋巴结,较少发生在颈部淋巴结,但其他淋巴结也可能受累。结外CAD很少见。我们报告一名72岁女性,几个月前出现了弥漫性2至5厘米的皮肤结节。患者接受了活检,病变在4个月内消退。除了轻度关节疼痛外,患者没有症状。组织病理学检查结果显示,有一个边界清楚的结节,由生发中心收缩和外套层扩大的淋巴滤泡组成。淋巴滤泡被硬化胶原的血管周围带分隔。滤泡之间存在上皮样和树突状组织细胞聚集,伴有明显的淋巴浆细胞浸润和血管增生。虽然皮肤结外CAD已有报道,但我们认为这是首例无淋巴结受累证据的多中心皮肤CAD病例。

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