Briselli M, Mark E J, Dickersin G R
Cancer. 1981 Jun 1;47(11):2678-89. doi: 10.1002/1097-0142(19810601)47:11<2678::aid-cncr2820471126>3.0.co;2-9.
Three-hundred-sixty cases of solitary fibrous tumor of the pleura from the literature are analyzed, and eight new cases are described. Of patients reported on prior to 1972, 72% had symptoms due to the tumor at the time of diagnosis, but only 54% of patients reported on since then were symptomatic. This probably reflects earlier diagnosis as a result of increased use of chest radiographs in asymptomatic populations. Cough, chest pain, dyspnea, and/or pulmonary osteoarthropathy are each found in at least one-third of patients who have symptoms. Approximately 80% of solitary fibrous tumors of the pleura originate in the visceral and 20% in the parietal pleura. In the literature and in this experience these tumors are on the whole circumscribed. The range in size from 1-36 cm with a mean of 6 cm. Many are pedunculated on pleural-based pedicles that contain hypertrophic arteries and veins. Histologic examination of the tumor usually discloses cellular areas alternating with hyalinized and/or necrotic areas. Spindle-shaped cells typically have minimal nuclear pleomorphism and rare or absent mitoses. Numerous thin-walled vessels constitute an additional feature of large tumors. Electron microscopical examination reveals features of both fibroblasts and mesothelial cells. Solitary fibrous tumors behave in a benign fashion in 88% of cases after surgical resection. In 12% of the cases the tumor is responsible for the patient's death because of its extensive intrathoracic growth, by virtue of either late diagnosis or unresectable recurrence. No single histologic feature allows a definite prognosis. The best indicator of a good prognosis is the presence of a pedicle supporting the tumor. Also favorable in circumscription of the tumor without invasion of lung, mediastinum, or chest wall. Nuclear pleomorphism and a high mitotic rate are seen in larger tumors but do not necessarily indicate a poor prognosis if the tumor is circumscribed. Solitary fibrous tumors of the pleura are not associated with asbestos.
对文献中360例胸膜孤立性纤维瘤进行了分析,并描述了8例新病例。在1972年之前报告的患者中,72%在诊断时因肿瘤出现症状,但此后报告的患者中只有54%有症状。这可能反映了由于在无症状人群中增加使用胸部X光片而导致的早期诊断。咳嗽、胸痛、呼吸困难和/或肺性骨关节病在至少三分之一有症状的患者中均有发现。大约80%的胸膜孤立性纤维瘤起源于脏层胸膜,20%起源于壁层胸膜。在文献和本研究中,这些肿瘤总体上边界清晰。大小范围为1至36厘米,平均为6厘米。许多肿瘤有蒂,附着于含有肥厚动静脉的胸膜蒂上。肿瘤的组织学检查通常显示细胞区域与透明变性和/或坏死区域交替出现。梭形细胞通常核异形性极小,有丝分裂罕见或无。大量薄壁血管是大肿瘤的另一个特征。电子显微镜检查显示有成纤维细胞和间皮细胞的特征。胸膜孤立性纤维瘤在手术切除后88%的病例中表现为良性。在12%的病例中,肿瘤导致患者死亡,原因是其在胸腔内广泛生长,要么是诊断延迟,要么是复发无法切除。没有单一的组织学特征可以明确预后。良好预后的最佳指标是存在支持肿瘤的蒂。肿瘤边界清晰且未侵犯肺、纵隔或胸壁也较为有利。在较大的肿瘤中可见核异形性和高有丝分裂率,但如果肿瘤边界清晰,不一定表明预后不良。胸膜孤立性纤维瘤与石棉无关。