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[腹膜假黏液瘤合并阑尾黏液性囊腺瘤。1例报告并文献复习]

[Pseudomyxoma peritonei associated with appendiceal mucinous cystadenoma. Report of a case and review of the literature].

作者信息

Hernandez C A, Ruiz M E, Urdaneta M T

出版信息

G E N. 1994 Jul-Sep;48(3):157-62.

PMID:7768420
Abstract

Mucinous cystadenoma of the appendix is a rare entity. Its incidence is low, between 0.1 and 0.3%. Constitutes are found incidentally al surgery and is generally asymptomatic. We present a case of a 60 years old woman which was complicated by a pseudomyxoma peritonei, idiopathic ulcerative rectocolitis and infiltration of the muscular layer of the colon sigmoid wall with poorly differentiated adenocarcinoma. We reviewed the literature, emphasize modern concepts about its terminology and its possible pathogenesis.

摘要

阑尾黏液性囊腺瘤是一种罕见的疾病。其发病率较低,在0.1%至0.3%之间。通常在手术中偶然发现,一般无症状。我们报告一例60岁女性病例,该病例并发腹膜假黏液瘤、特发性溃疡性直肠结肠炎以及乙状结肠壁肌层被低分化腺癌浸润。我们回顾了文献,强调了关于其术语和可能发病机制的现代概念。

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