Hartmann C A, Schütze H
Institute for Pathology, Klinikum Steglitz, Berlin, Germany.
J Cancer Res Clin Oncol. 1994;120(6):331-47. doi: 10.1007/BF01247458.
The 72 mesothelioma-like tumors of the pleura (MLTP) found among 33 500 autopsy cases collected over more than 30 years are reviewed. MLTP have a worse prognosis than the 106 cases of pleural mesothelioma autopsied in our institutes with regard to survival time and metastatic spread. In MLTP, adenocarcinomas predominate with a wide range of histological and cytological variation and prominent development of connective tissue having its origin in the periphery of the lung. These intrapulmonary primary tumors often fulfill the criteria of pulmonary scar cancer. Etiologically, there is no correlation between the origin of this tumor and smoking or exposure to asbestos. The absence of mucus formation and glandular differentiation, together with the presence of spindle-shaped carcinoma components and strong mesothelial or stroma proliferation, can make the differential diagnosis between this tumor type and mesothelioma difficult. Immunohistological investigations were performed on 11 cases with antibodies against intermediate filament proteins, vascular endothelium, collagen IV, macrophage antigens, carcinoembryonic antigen (CEA), LeuM1, and the antibody BerEP4. Our investigation shows that a battery of several tumor markers, such as antibodies against LeuM1, CEA, and the antibody BerEP4, as well as staining with periodic acid/Schiff/diastase discriminate primary from secondary pleural neoplasms, whilst intermediate filament proteins alone are of little diagnostic value.
回顾了在30多年间收集的33500例尸检病例中发现的72例胸膜间皮瘤样肿瘤(MLTP)。就生存时间和转移扩散而言,MLTP的预后比我们机构尸检的106例胸膜间皮瘤更差。在MLTP中,腺癌占主导,具有广泛的组织学和细胞学变异,并且起源于肺周边的结缔组织显著发育。这些肺内原发性肿瘤常符合肺瘢痕癌的标准。从病因学上看,该肿瘤的起源与吸烟或接触石棉无关。缺乏黏液形成和腺分化,以及存在梭形癌成分和强烈的间皮或基质增殖,会使这种肿瘤类型与间皮瘤的鉴别诊断变得困难。对11例病例进行了免疫组织学研究,使用了针对中间丝蛋白、血管内皮、IV型胶原、巨噬细胞抗原、癌胚抗原(CEA)、LeuM1以及抗体BerEP4的抗体。我们的研究表明,一系列多种肿瘤标志物,如针对LeuM1、CEA的抗体以及抗体BerEP4,以及过碘酸/希夫/淀粉酶染色可区分原发性和继发性胸膜肿瘤,而仅中间丝蛋白的诊断价值不大。