原发性肺黏液性囊腺癌：一例报告

Efstathiou Andreas, Asteriou Christos, Barbetakis Nikolaos, Miliaras Dimosthenis, Kleontas Athanassios, Karvelas Christos, Lalountas Miltiadis

Cardiothoracic Surgery Department, Theagenio Cancer Hospital, Al. Symeonidi 2, 54007 Thessaloniki, Greece.

Case Rep Med. 2011;2011:562026. doi: 10.1155/2011/562026. Epub 2011 Mar 29.

Primary pulmonary mucinous cystadenocarcinoma (PMCAC) is an extremely rare cystic neoplasm. A case of a 56-year-old male with a cystic lesion of the right lower lobe is described. Preoperative fine needle aspiration cytology and bronchoscopy were inconclusive. The patient underwent a formal right lower lobectomy and mediastinal lymph node dissection. Diagnosis was established intraoperatively. The biological behavior of primary PMCAC is unknown. Therefore, careful long-term follow-up is considered necessary because of lack of experience globally.

原发性肺黏液性囊腺癌（PMCAC）是一种极为罕见的囊性肿瘤。本文描述了一例56岁男性右下叶囊性病变的病例。术前细针穿刺细胞学检查和支气管镜检查结果不明确。患者接受了正规的右下叶切除术和纵隔淋巴结清扫术。术中确诊。原发性PMCAC的生物学行为尚不清楚。因此，鉴于全球范围内缺乏经验，谨慎的长期随访被认为是必要的。