Alkhalil Nayef, Al Omary Abdullah
Gastroenterology Department, Lebanese University - Faculty of Medical Sciences, Beirut, LBN.
Gastroenterology Department, Rafik Hariri University Hospital (RHUH), Beirut, LBN.
Cureus. 2024 Apr 8;16(4):e57857. doi: 10.7759/cureus.57857. eCollection 2024 Apr.
Pseudomyxoma peritonei (PMP) is a rare intra-abdominal malignancy characterized by diffuse dissemination of mucinous tumor cells, leading to mucinous ascites. Accurate diagnosis is crucial for appropriate management. This report presents a case of a 55-year-old Lebanese male farmer initially misdiagnosed with liver cirrhosis who presented with progressive abdominal distension refractory to diuretics and dietary modifications. Paracentesis revealed a mucinous exudate, with subsequent clinical and histopathological examination confirming PMP. The patient was referred for further evaluation at a specialized center equipped for cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC). This case highlights the diagnostic challenges of PMP due to its non-specific presentation, emphasizing the importance of prompt and accurate diagnosis to facilitate optimal therapeutic intervention.
腹膜假黏液瘤(PMP)是一种罕见的腹腔内恶性肿瘤,其特征是黏液性肿瘤细胞弥漫性播散,导致黏液性腹水。准确诊断对于恰当的治疗管理至关重要。本报告介绍了一例55岁的黎巴嫩男性农民病例,该患者最初被误诊为肝硬化,表现为进行性腹胀,对利尿剂和饮食调整无效。腹腔穿刺抽出黏液性渗出液,随后的临床和组织病理学检查确诊为PMP。该患者被转诊至一家配备了细胞减灭术(CRS)和腹腔内热灌注化疗(HIPEC)的专业中心进行进一步评估。该病例凸显了PMP因其非特异性表现而带来的诊断挑战,强调了及时准确诊断对于促进最佳治疗干预的重要性。