肺纤毛黏结乳头状瘤的手术治疗(附11例报告)

Z. Wan, Wei Huang, G. Jiang, L. Hou
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摘要

目的探讨肺纤毛结节状乳头状瘤的临床特点。方法回顾性分析2017年4月至2018年4月我科11例最终病理诊断为CMPT的病例。男性8例,女性3例,平均年龄(63.7±5.6)岁。对临床资料、组织病理特征、治疗及预后进行综述。所有患者术前均行CT扫描。结果CMPT的影像学表现为:位于周围,多位于右下叶;大多数CMPT病变呈GGO状,部分中心有气隙,少数实性灶。所有患者均成功行胸腔镜手术(VATS),无严重围手术期并发症。平均手术时间(78.0±28.2)min,平均失血量(37.3±14.9)ml,平均住院时间(3.45±0.93)d。所有患者均行CMPT病理检查。随访6 ~ 18个月,无复发。结论CMPT是一种罕见的肿瘤,无特异性临床表现,易误诊为原位腺癌或微创腺癌。VATS治疗CMPT可行、安全,预后良好。关键词:肺部肿瘤纤毛结节状乳头状肿瘤胸腔镜手术预后
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Surgical treatment of ciliated muconodular papillary tumor of the lung: a report of 11 cases
Objective To investigate the clinical features of ciliated muconodular papillary tumor(CMPT) of the lung. Methods We retrospectively reviewed 11 cases with final pathology being diagnosed as CMPT in our department from April 2017 to April 2018. There were 8 males and 3 females with a mean age of(63.7±5.6) years. The clinical data, histopathological features, treatment, and prognosis were reviewed. All patients received CT scan before operation. Results The radiological features of CMPT include: located peripherally and most in right lower lobe; most CMPT lesions are GGO, some with air spaces in center and few being solid. All patients underwent video-assisted thoracic surgery(VATS) successfully, and there were no severe perioperative complications. The mean operating time was(78.0±28.2) min. The mean blood loss was(37.3±14.9) ml. The mean postoperative hospital stays were(3.45±0.93) days. Pathology examination of all patients were CMPT. Follow-up time ranged from 6 to 18 months and no recurrence was found. Conclusion CMPT is rare tumor, without specific clinical manifestation, but sometimes misdiagnosed as adenocarcinoma in situ or minimally invasive adenocarcinoma. VATS is feasible and safe for CMPT, and the prognosis is good. Key words: Pulmonary neoplasms Ciliated muconodular papillary tumor Video-assisted thoracic surgery Prognosis
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