Vimercati Luigi, Cavone Domenica, Delfino Maria Celeste, Bruni Biagio, De Maria Luigi, Caputi Antonio, Sponselli Stefania, Rossi Roberta, Resta Leonardo, Fortarezza Francesco, Pezzuto Federica, Serio Gabriella
Interdisciplinary Department of Medicine, Occupational Medicine-Section Ramazzini, University of Bari Aldo Moro, 70124 Bari, Italy.
Ultrastructure Laboratory, Istituto Superiore di Sanità, 00161 Rome, Italy.
Cancers (Basel). 2021 May 10;13(9):2278. doi: 10.3390/cancers13092278.
Primary ovarian mesothelioma is a rare, aggressive neoplastic disease with a poor prognosis. At onset, the tumor is only rarely limited to the ovaries and usually already widespread in the peritoneum. The rarity of this entity and the difficulties differentiating it from either ovarian carcinoma or peritoneal mesothelioma may lead to frequent misdiagnoses and may raise some concerns about its histogenesis. Thus, reporting such rare cases is fundamental to gain greater awareness of this neoplasm and try to answer unsolved questions. Herein, we described four cases of histological diagnoses of ovarian mesothelioma extrapolated by the regional mesothelioma register of Apulia (southern Italy). In all cases, a detailed medical history was collected according to national mesothelioma register guidelines. A broad panel of antibodies was used for immunohistochemistry to confirm the diagnoses. Moreover, ovarian tissue samples were also examined by transmission and scanning electron microscopy, detecting asbestos fibers and talc crystals in two cases. Because of the few cases described, we reviewed the English literature in the Medline database, focusing on articles about ovarian mesothelioma "misclassification", "misdiagnosis", "diagnostic challenge" or "diagnostic pitfall" and on unsolved questions about its histogenesis and possible risk factors.
原发性卵巢间皮瘤是一种罕见的侵袭性肿瘤性疾病,预后较差。发病时,肿瘤很少仅局限于卵巢,通常已广泛累及腹膜。这种实体瘤的罕见性以及将其与卵巢癌或腹膜间皮瘤区分开来的困难,可能导致频繁误诊,并可能引发对其组织发生的一些疑问。因此,报告此类罕见病例对于提高对这种肿瘤的认识并试图回答未解决的问题至关重要。在此,我们描述了4例通过意大利南部普利亚地区间皮瘤登记处推断出组织学诊断为卵巢间皮瘤的病例。在所有病例中,均根据国家间皮瘤登记指南收集了详细的病史。使用了一系列广泛的抗体进行免疫组织化学检查以确诊。此外,还对卵巢组织样本进行了透射和扫描电子显微镜检查,在2例中检测到了石棉纤维和滑石晶体。由于所描述的病例较少,我们在Medline数据库中查阅了英文文献,重点关注有关卵巢间皮瘤“错误分类”“误诊”“诊断挑战”或“诊断陷阱”的文章,以及有关其组织发生和可能危险因素的未解决问题。