Corsale I, Agozzino L, Nappo C, Corsale C
Istituto di Anatomia ed Istologia Patologica, II Università degli Studi, Napoli.
Minerva Chir. 1999 Jul-Aug;54(7-8):513-7.
Multicystic peritoneal mesothelioma is an extremely rare benign neoplastic disease with high tendency to recur locally, but no tendency to malignancy. Correct diagnosis can be made with histopathologic examination and always with immunohistochemical and ultrastructural evaluation. A case in a twenty-eight-year-old woman is reported and the anatomo-clinical characteristics of multicystic peritoneal mesothelioma from sixty-nine cases described in the literature are specified, discussing the management of this disease and emphasizing the importance of a nondemolitive approach.
多囊性腹膜间皮瘤是一种极其罕见的良性肿瘤性疾病,具有较高的局部复发倾向,但无恶变倾向。通过组织病理学检查,并结合免疫组织化学和超微结构评估可做出正确诊断。本文报告了一例28岁女性病例,并详细说明了文献中描述的69例多囊性腹膜间皮瘤的解剖学和临床特征,讨论了该疾病的治疗方法,并强调了非破坏性治疗方法的重要性。