Pseudomyxomaperitonei (PMP) is a rare disease characterized by presence of gelatinous ascites and mucinous implants on the peritoneum and omentum. We report the case of a 58 years old woman with primary tumour of the appendix and secondary involvement of other structures & organs of abdominal cavity. Aim of this case report is to create awareness among the clinicians regarding this uncommon disease presented with ascites and irregular masses in the abdomen. In addition, literature on the clinical presentation, diagnostic procedures, and treatment options has been briefly reviewed. Pulse Vol.10 January-December 2017 p.47-51

中文翻译：

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Pseudomyxomaperitonei：一种罕见的临床实体——病例报告

Pseudomyxomaperitonei (PMP) 是一种罕见的疾病，其特征是在腹膜和网膜上存在凝胶状腹水和粘液植入物。我们报告了一例 58 岁女性，原发性阑尾肿瘤和腹腔其他结构和器官继发性受累。本病例报告的目的是提高临床医生对这种以腹水和腹部不规则肿块为表现的罕见疾病的认识。此外，还简要回顾了有关临床表现、诊断程序和治疗方案的文献。Pulse Vol.10 2017 年 1 月-12 月 p.47-51