Literature DB >> 17723965

Pseudomyxoma peritonei syndrome of appendiceal origin: an overview.

Carol Brueggen1, Gayle Baird, Allison Meisheid.   

Abstract

Pseudomyxoma peritonei (PMP) syndrome is an uncommon, slowly progressive condition that usually arises from perforation of an adenoma in the appendix. PMP syndrome is characterized by mucin accumulation in the peritoneal cavity. Mucinous implants are found on all peritoneal surfaces and the omentum. PMP syndrome rarely metastasizes outside the abdominal cavity but remains a fatal illness as the space in the abdomen and pelvis required for normal function of the gastrointestinal tract becomes filled with copious amounts of the mucinous tumor. Treatment options include observation, aggressive debulking surgery, intraperitoneal chemotherapy, radiotherapy, and mucolytic agents.

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Year:  2007        PMID: 17723965     DOI: 10.1188/07.CJON.525-532

Source DB:  PubMed          Journal:  Clin J Oncol Nurs        ISSN: 1092-1095            Impact factor:   1.027


  3 in total

1.  Application of advanced multimodality care to pseudomyxoma peritonei patient: report of first patient treated at a tertiary center.

Authors:  Arshad Bashir Khan; Youssuf Al Suhaibani; Khaled Al Mohaimed; David L Morris
Journal:  Indian J Surg Oncol       Date:  2010-12-23

2.  Enteral nutrition provides favorable postoperative outcomes for patients with pseudomyxoma peritonei: a retrospective study.

Authors:  Xuechun Kuang; Guie She; Yanhui Shi; Zhiyou Yang; Jun Li; Zhipeng Zhang
Journal:  Gland Surg       Date:  2022-05

3.  Different medical expenses incurred by appendiceal cystadenoma in China: Report of three cases.

Authors:  Guo-Sheng Wang; Liu Yang; Hai-Fen Ma; Yuan Gao
Journal:  Oncol Lett       Date:  2013-02-04       Impact factor: 2.967

  3 in total

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