Yamada S, Ogawa J, Inoue H, Syohtsu H
1st Department of Surgery, School of Medicine, Tokai University, Kanagawa, Japan.
Kyobu Geka. 1994 May;47(5):383-6.
Six so-called rare pulmonary tumors, resected at the hospital are reported. Histologically there were pulmonary blastoma, pulmonary adenocarcinoma of fetal lung type, alveolar soft part sarcoma, oncocytic carcinoid tumor, hemangioendothelioma, and leiomyoma in each one case. The represented about 1.5% of all resected lung tumors. The age of these patients ranged from 28 to 67 years old, and all were females. Two patients experienced hemosuputum, but the others have no clinical symptoms. All the patients showed relatively well circumscribed mass shadows on chest X-ray films, but none could have accurate diagnosis by preoperative examinations. One patient with alveolar soft part sarcoma died of brain metastasis 18 months after the resection, however, the other 5 patients remained well from 2 year 7 months to 11 years after the surgery.
本文报告了在该医院切除的6例所谓的罕见肺部肿瘤。组织学检查结果显示，分别为1例肺母细胞瘤、1例胎儿型肺腺癌、1例肺泡软组织肉瘤、1例嗜酸性细胞瘤样肿瘤、1例血管内皮瘤和平滑肌瘤。这些病例约占所有切除的肺部肿瘤的1.5%。这些患者的年龄在28岁至67岁之间，均为女性。2例患者出现咯血痰，其他患者无临床症状。所有患者在胸部X光片上均显示出边界相对清晰的肿块阴影，但术前检查均无法做出准确诊断。1例肺泡软组织肉瘤患者在切除术后18个月死于脑转移，然而，其他5例患者在手术后2年7个月至11年期间情况良好。
