[肠系膜Castleman病合并胃炎性肌瘤息肉1例报告及文献复习]。

Chirurgia italiana Pub Date : 2009-03-01
Mauro Andreano, Vito D'Ambrosio, Massimo Antropoli, Raffaele Fioretto, Luciano Vicenzo, Marco Clemente
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引用次数: 0

摘要

Castleman氏病是一种非常罕见的疾病,在诊断和治疗上都存在许多问题。它通常与其他疾病有关,可以在身体的任何部位发展。Castleman病可根据临床和放射学表现分为单中心型和多中心型,根据组织学特征分为透明血管型和浆细胞型,根据患者的HIV感染状况分为HIV相关型和非HIV相关型。炎性肌瘤息肉是一种非常罕见的良性病变,可以在胃肠道的任何地方发展。这种息肉最常见于胃窦,通常发生在50至60岁的人群中。作者报告了一名41岁女性的肠系膜Castleman病和胃炎性肌瘤息肉的不寻常发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Mesenteric Castleman's disease and inflammatory fibroid polyp of the stomach: a case report and review of the literature].

Castleman's disease is a very rare disease that causes many problems both in diagnosis and therapy. It is often associated with other diseases and can develop in any part of the body. Castleman's disease can be classified as uni-centric or multicentric based on clinical and radiological findings, as hyaline-vascular or plasma-cell based on the histological aspect, and as HIV-related or non-HIV-related, based on the HIV status of the patient. An inflammatory fibroid polyp is a very rare benign lesion that can develop anywhere in the gastrointestinal tract. Such polyps are most commonly found in the gastric antrum and usually occur in 50- to 60-year-old people. The authors report the unusual finding of mesenteric Castleman's disease and an inflammatory fibroid polyp of the stomach in a 41-year-old woman.

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