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[孤立性腹膜后Castleman病]

[Isolated retroperitoneal Castleman's disease].

作者信息

Roşca Maria-Gabriela, Mariciuc D, Ferariu D, Scripcariu V

机构信息

Facultatea de Medicină, Clinica a III-a Chirurgie, Universitatea de Medicină si Farmacie "Gr.T. Popa" Iaşi.

出版信息

Rev Med Chir Soc Med Nat Iasi. 2008 Jul-Sep;112(3):698-702.

Abstract

Castleman's disease is a rare disorder characterized by proliferation of the lymphoid tissue. Castleman's disease affects both males and females, and may occur at any age. Little is known about how often Castleman's disease actually occurs, other than it is rare, or what causes the disease. The most frequent location of the disease is the mediastinum. The location of the disease in the retroperitoneum is rare and it is usually associated with the generalized form of the disease. We report a case of a 34-year old man with isolated retroperitoneum Castleman's disease of the hyaline-vascular type, which presented as a palpable abdominal mass. The final diagnosis was reached after exploratory laparotomy and resection of the tumor.

摘要

卡斯特leman病是一种罕见的疾病,其特征为淋巴组织增生。卡斯特leman病可发生于男性和女性,且可在任何年龄出现。除了它很罕见之外,对于卡斯特leman病实际的发病频率以及病因知之甚少。该疾病最常见的部位是纵隔。疾病位于腹膜后的情况罕见,且通常与疾病的全身型相关。我们报告一例34岁男性患有孤立性腹膜后透明血管型卡斯特leman病,表现为可触及的腹部肿块。经剖腹探查及肿瘤切除后得出最终诊断。

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