Z. Amzal, M. Kadiri, M. Borahma, F. Chabib, N. Lagdali, C. Berhili, I. Benelbarhdadi, F. Ajana
{"title":"Appendicular Mucocele Complicated by Peritoneal Pseudomyxoma","authors":"Z. Amzal, M. Kadiri, M. Borahma, F. Chabib, N. Lagdali, C. Berhili, I. Benelbarhdadi, F. Ajana","doi":"10.36348/sjpm.2024.v09i01.004","DOIUrl":null,"url":null,"abstract":"Appendiceal mucocele (AM) or Appendiceal mucinous neoplasms is a rare but potentially dangerous condition. In the latter, a spontaneous or iatrogenic rupture of the mucocele can lead to mucinous intraperitoneal ascites, a syndrome known as pseudomyxoma peritonei. We present the case of a 76-year-old female patient who reported right iliac fossa pain with RIF tenderness on clinical examination, and underwent an abdominal CT scan showing an appendiceal mucocele associated with a small peritoneal effusion suspecting a ruptured mucocele, related to peritoneal pseudomyxoma. The patient underwent appendectomy with peritoneal lavage and aspiration of all mucin found. Anatomopathological analysis confirmed the diagnosis of appendiceal mucocele (a low-grade appendiceal mucinous neoplasm).","PeriodicalId":471257,"journal":{"name":"Saudi journal of pathology and microbiology","volume":"38 9","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Saudi journal of pathology and microbiology","FirstCategoryId":"0","ListUrlMain":"https://doi.org/10.36348/sjpm.2024.v09i01.004","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Appendiceal mucocele (AM) or Appendiceal mucinous neoplasms is a rare but potentially dangerous condition. In the latter, a spontaneous or iatrogenic rupture of the mucocele can lead to mucinous intraperitoneal ascites, a syndrome known as pseudomyxoma peritonei. We present the case of a 76-year-old female patient who reported right iliac fossa pain with RIF tenderness on clinical examination, and underwent an abdominal CT scan showing an appendiceal mucocele associated with a small peritoneal effusion suspecting a ruptured mucocele, related to peritoneal pseudomyxoma. The patient underwent appendectomy with peritoneal lavage and aspiration of all mucin found. Anatomopathological analysis confirmed the diagnosis of appendiceal mucocele (a low-grade appendiceal mucinous neoplasm).