Literature DB >> 16532086

Pseudomyxoma peritonei.

Abdul-Wahed N Meshikhes1, Hussain A Al-Abkari, Sami A Al-Momen, Feryal E Saad.   

Abstract

Pseudomyxoma peritonei is very rare, and its exact pathogenesis is unknown. It is characterized by intra-abdominal extracellular gelatinous fluid collections. We report a case of pseudomyxoma peritonei in a 38-year-old Saudi male who presented with right iliac fossa mass and weight loss. He was treated initially as an appendicular mass and computed tomography was helpful in making the diagnosis. He was treated by laparotomy, right hemicolectomy and omentectomy, but no perioperative intraperitoneal chemotherapy was instilled. He received postoperative chemotherapy and remained alive with no recurrence at 18-month follow-up.

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Mesh:

Year:  2006        PMID: 16532086

Source DB:  PubMed          Journal:  Saudi Med J        ISSN: 0379-5284            Impact factor:   1.484


  2 in total

1.  Psuedomyxoma peritonei secondary to adenocarcinoma of the cecum.

Authors:  Hussah Al-Buainain; Yasser Al-Jehani; Khaled Moghazy; Abdulaziz Al-Quorain
Journal:  J Family Community Med       Date:  2010-05

2.  Pseudomyxoma peritonei: a clinical case of this poorly understood condition.

Authors:  Ana Maria de Oliveira; Catarina Graça Rodrigues; Alexys Borges; Alexandra Martins; Sofia Loureiro Dos Santos; Francisco Rocha Pires; João Mascarenhas Araújo; João Ramos de Deus
Journal:  Int J Gen Med       Date:  2014-03-03
  2 in total

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