Salemis Nikolaos S, Tsiambas Evangelos, Gourgiotis Stavros, Mela Ageliki, Karameris Andreas, Tsohataridis Efstathios
2nd Department of Surgery, 417 Army Veterans General Hospital NIMTS, Athens, Greece.
J Dig Dis. 2007 Nov;8(4):216-21. doi: 10.1111/j.1751-2980.2007.00309.x.
Peritoneal mesothelioma is a rare disease associated with poor prognosis. Acute abdomen as the first presentation is an extremely rare occurrence. We report an exceptional case of a patient who was found to have a jejunal perforation due to infiltration of peritoneal mesothelioma.
A 62-year-old man was admitted with clinical signs of peritonitis. Computerized tomographic scans showed a mass distal to the ligament of Treitz, thickening of the mesentery and a small amount of ascites.
Emergency laparotomy revealed a perforated tumor 15 cm distal to the ligament of Treitz and diffuse peritoneal disease. Segmental small bowel resection and suboptimal cytoreduction were performed. Histopathology and immunohistochemistry showed infiltration of malignant mesothelioma. During the postoperative period pleural mesothelioma was also diagnosed. Despite adjuvant chemotherapy, the patient died of disseminated progressive disease 7 months after surgery.
Peritoneal mesothelioma is a rare malignancy with grim prognosis. Small bowel involvement is a poor prognostic indicator. Our case of a small bowel perforation due to direct infiltration by peritoneal mesothelioma appears to be the first reported in the English literature.
腹膜间皮瘤是一种罕见疾病,预后较差。以急腹症为首发表现极为罕见。我们报告一例特殊病例,该患者因腹膜间皮瘤浸润导致空肠穿孔。
一名62岁男性因腹膜炎临床症状入院。计算机断层扫描显示在Treitz韧带远端有一肿块、肠系膜增厚及少量腹水。
急诊剖腹探查发现Treitz韧带远端15 cm处有一穿孔性肿瘤及弥漫性腹膜病变。行节段性小肠切除术及减瘤不彻底手术。组织病理学和免疫组化显示为恶性间皮瘤浸润。术后期间还诊断出胸膜间皮瘤。尽管进行了辅助化疗,患者术后7个月死于播散性进展性疾病。
腹膜间皮瘤是一种罕见的恶性肿瘤,预后严峻。小肠受累是预后不良的指标。我们报道的这例因腹膜间皮瘤直接浸润导致小肠穿孔的病例似乎是英文文献中首例报道。