Shyu H L, Huang B S, Cheng C Y, Wu J K, Wang L S, Hsu W H, Tao C W, Li W Y, Huang M H, Chien K Y
Department of Surgery, Veterans General Hospital-Taipei, Taiwan, R.O.C.
Zhonghua Yi Xue Za Zhi (Taipei). 1994 Jun;53(6):363-8.
Carcinosarcoma of the lung is a rare malignant pulmonary neoplasm, and constitutes 0.1% to 0.3% of all lung tumors. Typically, these tumor have both carcinomatous and sarcomatous components with a poor prognosis due to late diagnosis and early metastases.
From July 1980 to December 1993, six patients with pulmonary carcinosarcoma who underwent surgical treatment were studied. None of them had accurate tissue diagnosis before operation except one case with peripheral variant carcinosarcoma who was diagnosed by percutaneous transthoracic fine needle biopsy under sonographic guidance. All of our patients had a huge peripheral lung tumor 3.8 to 10 cm in diameter. Pneumonectomy was done in two patients, and lobectomy in three. The other patient had unresectable tumor.
The histopathological components in carcinoma were epidermoid carcinoma in and adenocarcinoma in 3. Differentiation of sarcomatous lesions included spindle cell sarcoma in 3, fibrosarcoma in 2 and undifferentiated mesenchymal sarcoma in one patient. In the resectable group, 1 was at stage II and 4 were at stage IIIa. None of the patients survived more than 2 years due to distant metastasis and cachexia. The mean survival was 140 days.
The carcinomatous portion tends to metastasize to regional lymph nodes whereas the sarcomatous part gives rise to systemic dissemination. Due to early systemic dissemination and poor prognosis, combination of extensive surgical intervention resection with aggressive postoperative chemotherapy and radiotherapy might be a reasonable consideration to improve survival in primary pulmonary carcinosarcoma.
肺肉瘤样癌是一种罕见的肺部恶性肿瘤,占所有肺部肿瘤的0.1%至0.3%。通常,这些肿瘤同时具有癌性和肉瘤性成分,由于诊断较晚和早期转移,预后较差。
对1980年7月至1993年12月期间接受手术治疗的6例肺肉瘤样癌患者进行研究。除1例周围型变异型肉瘤样癌患者在超声引导下经皮经胸细针穿刺活检确诊外,其余患者术前均未获得准确的组织学诊断。所有患者均有一个直径3.8至10 cm的巨大周围型肺肿瘤。2例行全肺切除术,3例行肺叶切除术。另一例患者肿瘤无法切除。
癌的组织病理学成分中,3例为鳞状细胞癌,3例为腺癌。肉瘤样病变的分化类型包括3例梭形细胞肉瘤、2例纤维肉瘤和1例未分化间叶肉瘤。在可切除组中,1例为Ⅱ期,4例为Ⅲa期。由于远处转移和恶病质,所有患者均未存活超过2年。平均生存期为140天。
癌性部分倾向于转移至区域淋巴结,而肉瘤样部分则引起全身播散。由于早期全身播散和预后较差,广泛的手术切除联合积极的术后化疗和放疗可能是提高原发性肺肉瘤样癌生存率的合理选择。