论文部分内容阅读
胸膜间皮瘤(Pleural Mesotheliama)是胸膜原发性肿瘤。来自胸膜下间皮组织和间质组织。其侵犯部位不同,临床表现各异。我院自1965～1990年间共收治17例胸膜间皮瘤病人。剖胸探查7例;胸膜活检8例;开颅探查1例(胸膜间皮瘤颅内转移);腹水细胞学检查1例。临床资料一、一般资料:男9例、女8例。年龄14～72岁,平均42.8岁。以青壮年多。发病至入院,最短半个月,最长36个月,平均7.6个月。二、临床症状(表1)、胸部X 线表现(表2)、病理类型(表3)。
Pleural Mesotheliama is a pleural primary tumor. From the subpleural mesothelial tissue and interstitial tissue. The invading parts are different and their clinical manifestations are different. In our hospital, 17 patients with pleural mesothelioma were treated from 1965 to 1990. Seven patients underwent exploratory thoracotomy; 8 underwent pleural biopsy; 1 underwent craniotomy (intracranial metastasis of pleural mesothelioma); and 1 patient underwent cytology of ascites. Clinical data 1. General information: 9 males and 8 females. Age 14 to 72 years old, average 42.8 years old. More young people. Onset to admission, the shortest half month, the longest 36 months, an average of 7.6 months. Second, clinical symptoms (Table 1), chest X-ray findings (Table 2), pathological types (Table 3).