中华肿瘤杂志
中華腫瘤雜誌
중화종류잡지
CHINESE JOURNAL OF ONCOLOGY
2014年
4期
282-286
,共5页
任剑飞%周建娅%丁伟%钟百书%周建英
任劍飛%週建婭%丁偉%鐘百書%週建英
임검비%주건아%정위%종백서%주건영
肺肿瘤%腺癌%临床病理学%体层摄影术,X线计算机%微乳头结构
肺腫瘤%腺癌%臨床病理學%體層攝影術,X線計算機%微乳頭結構
폐종류%선암%림상병이학%체층섭영술,X선계산궤%미유두결구
Lung neoplasm%Adenocarcinoma%Pathology,clinical%Tomography,X-ray computed%Micropapillary pattern
目的 探讨伴微乳头结构(MPP)肺腺癌的临床病理特征和影像学特点.方法 回顾性分析2011年7月至2012年12月手术切除的80例伴MPP肺腺癌患者的临床资料,分析其临床病理特征和影像学特点.结果 80例伴MPP的肺腺癌患者中,Ⅰ期38例(47.5%),Ⅱ期12例(15.0%),Ⅲ期25例(31.3%),Ⅳ期5例(6.2%).中分化14例(17.5%),中低分化66例(82.5%).有胸膜侵犯、脉管侵犯、支气管壁累及、大血管累及、神经侵犯和淋巴结转移其中之一者63例(78.8%).免疫组化结果显示,甲状腺转录因子1(TTT-1)和细胞角蛋白7(CK7)阳性率均为100%,表面活性剂载脂蛋白A(SPA)阳性率为84.0%.影像学检查结果显示,肺门或纵膈淋巴结肿大占18.8%,但病理确诊肺门或纵隔淋巴结转移者占45.0%.肺部影像以周围型为主,中央型较少,实性病灶多见,大部分伴分叶征、毛刺、胸膜凹陷征和血管集束征,磨玻璃影(GGO)和空泡征极少.结论 伴MPP的肺腺癌早期就出现胸膜、血管、淋巴管和淋巴结浸润.影像学表现为周围型和实性病灶为主,多伴分叶征、毛刺征、胸膜凹陷征和血管集束征等,GGO和空泡征较少.TTF-1、CK7、SPA高表达和癌胚抗原升高与临床分期有关.
目的 探討伴微乳頭結構(MPP)肺腺癌的臨床病理特徵和影像學特點.方法 迴顧性分析2011年7月至2012年12月手術切除的80例伴MPP肺腺癌患者的臨床資料,分析其臨床病理特徵和影像學特點.結果 80例伴MPP的肺腺癌患者中,Ⅰ期38例(47.5%),Ⅱ期12例(15.0%),Ⅲ期25例(31.3%),Ⅳ期5例(6.2%).中分化14例(17.5%),中低分化66例(82.5%).有胸膜侵犯、脈管侵犯、支氣管壁纍及、大血管纍及、神經侵犯和淋巴結轉移其中之一者63例(78.8%).免疫組化結果顯示,甲狀腺轉錄因子1(TTT-1)和細胞角蛋白7(CK7)暘性率均為100%,錶麵活性劑載脂蛋白A(SPA)暘性率為84.0%.影像學檢查結果顯示,肺門或縱膈淋巴結腫大佔18.8%,但病理確診肺門或縱隔淋巴結轉移者佔45.0%.肺部影像以週圍型為主,中央型較少,實性病竈多見,大部分伴分葉徵、毛刺、胸膜凹陷徵和血管集束徵,磨玻璃影(GGO)和空泡徵極少.結論 伴MPP的肺腺癌早期就齣現胸膜、血管、淋巴管和淋巴結浸潤.影像學錶現為週圍型和實性病竈為主,多伴分葉徵、毛刺徵、胸膜凹陷徵和血管集束徵等,GGO和空泡徵較少.TTF-1、CK7、SPA高錶達和癌胚抗原升高與臨床分期有關.
목적 탐토반미유두결구(MPP)폐선암적림상병리특정화영상학특점.방법 회고성분석2011년7월지2012년12월수술절제적80례반MPP폐선암환자적림상자료,분석기림상병리특정화영상학특점.결과 80례반MPP적폐선암환자중,Ⅰ기38례(47.5%),Ⅱ기12례(15.0%),Ⅲ기25례(31.3%),Ⅳ기5례(6.2%).중분화14례(17.5%),중저분화66례(82.5%).유흉막침범、맥관침범、지기관벽루급、대혈관루급、신경침범화림파결전이기중지일자63례(78.8%).면역조화결과현시,갑상선전록인자1(TTT-1)화세포각단백7(CK7)양성솔균위100%,표면활성제재지단백A(SPA)양성솔위84.0%.영상학검사결과현시,폐문혹종격림파결종대점18.8%,단병리학진폐문혹종격림파결전이자점45.0%.폐부영상이주위형위주,중앙형교소,실성병조다견,대부분반분협정、모자、흉막요함정화혈관집속정,마파리영(GGO)화공포정겁소.결론 반MPP적폐선암조기취출현흉막、혈관、림파관화림파결침윤.영상학표현위주위형화실성병조위주,다반분협정、모자정、흉막요함정화혈관집속정등,GGO화공포정교소.TTF-1、CK7、SPA고표체화암배항원승고여림상분기유관.
Objective To explore the clinicopathological characteristics and imaging features of lung adenocarcinoma with a micropapillary pattern (MPP).Methods Eighty cases of pulmonary adenocarcinoma with a micropapillary pattern treated in our hospital from July 2011 to December 2012 were selected to retrospectively analyze their clinicopathological characteristics and imaging features.Results Among the 80 cases of lung adenocarcinoma with MPP,there were 38 cases of stage Ⅰ (47.5%),12 cases of stage Ⅱ (15.0%),25 cases of stage Ⅲ (31.3%) and 5 cases of stage Ⅳ (6.2%).There were 14 cases of moderately differentiated (17.5%) and moderately/poorly differentiated (82.5%) tumors.Sixty-three cases had pleural involvement,vascular invasion,involving the bronchial wall,invasion of large vessels,nerve invasion,and lymph node metastasis (at least one of them) (78.8%).Immunohistochemical staining revealed that both positive rates of TTF-1 and CK7 were 100%,and that of pulmonary surfactant apolipoprotein-A (SPA) was 84.0%.Imaging examination revealed hilar or mediastinal lymph node enlargement in 15 cases (18.8%).but the pathology confirmed hilar or mediastinal lymph node metastasis in 36 cases (45.0%).Lung CT imaging showed that the majority of the cases were peripheral type,and only a few of central type,and most cases were solid lesions,with lobulation,spiculation,pleural indentation,and vascular convergence sign,while there were few ground-glass opacity sign and vacuole sign.Conclusions Lung adenocarcinoma with MPP component often presents with early invasions of pleura,blood vessels,lymphatic vessels,and lymph nodes.Imaging manifestation of this cancer mainly shows as peripheral and solid lesions,often with lobulation,spiculation,pleural indentation,vascular convergence sign,but GGO and vacuole signs are unusual.Overexpression of TTF-1,CK7 and SPA,and elevated CEA level are associated with clinical staging of the disease.