Kobashi Yoshihiro, Matsushima Toshiharu, Irei Tsutomu
Division of Respiratory Diseases, Department of Medicine, Kawasaki Medical School, Kurashiki, Japan.
Respirology. 2005 Nov;10(5):660-5. doi: 10.1111/j.1440-1843.2005.00765.x.
The aim of this study was to evaluate the clinicopathological features of lung cancer resembling malignant pleural mesothelioma.
The seven patients studied had tumours showing an extensive pleural growth pattern, and were chosen from 1516 lung cancer patients diagnosed at two affiliated hospitals over a 17-year period.
Histologically, five of these lung cancers were adenocarcinomas, one was a small cell carcinoma, and one a large cell carcinoma. Tumour markers such as carcinoembryonic antigen (CEA) were elevated in six patients at admission. However, a clinical diagnosis was difficult and these cancers could only be distinguished from malignant pleural mesothelioma by thoracentesis in two cases, pleural biopsy in two, thoracotomy in two, and in case 7 at autopsy. Treatment consisted of chemotherapy or radiation therapy in four patients, but with little clinical effect. The mean survival time was 6.7 months, which is much less than for true malignant pleural mesothelioma.
Lung cancer resembling malignant pleural mesothelioma is most frequently observed in patients with adenocarcinoma, which is suspected to occur peripherally. To distinguish pseudomesotheliomatous carcinoma from malignant pleural mesothelioma in patients with diffuse pleural thickening and effusion, requires adequate tissue sampling by thoracotomy or video-assisted thoracoscopic surgery and a panel of immunohistochemical stains.
本研究旨在评估类似恶性胸膜间皮瘤的肺癌的临床病理特征。
所研究的7例患者的肿瘤呈现广泛的胸膜生长模式,这些患者是从17年间在两家附属医院确诊的1516例肺癌患者中挑选出来的。
组织学上,这些肺癌中5例为腺癌,1例为小细胞癌,1例为大细胞癌。6例患者入院时癌胚抗原(CEA)等肿瘤标志物升高。然而,临床诊断困难,这些癌症仅在2例中通过胸腔穿刺、2例通过胸膜活检、2例通过开胸手术以及第7例在尸检时才与恶性胸膜间皮瘤区分开来。4例患者接受了化疗或放疗,但临床效果甚微。平均生存时间为6.7个月,远低于真正的恶性胸膜间皮瘤。
类似恶性胸膜间皮瘤的肺癌最常见于腺癌患者,推测其发生于外周。对于弥漫性胸膜增厚和胸腔积液患者,要将假间皮瘤样癌与恶性胸膜间皮瘤区分开来,需要通过开胸手术或电视辅助胸腔镜手术获取足够的组织样本,并进行一组免疫组织化学染色。