肺软骨瘤型错构瘤16例临床分析
|
摘要
<正>肺软骨瘤型错构瘤是胚胎时期异常发育肿瘤,是肺错构瘤中少见的一种类型,区别于肺软骨瘤、Carney三联征、肺纤维平滑肌瘤型错构瘤、结核球、周围型肺癌等,本文回顾性分析2001年1月至2017年10月郑州大学第一附属医院收治的16例肺软骨瘤型错构瘤患者的临床资料,以提高对该病的认识、诊断及治疗。1资料与方法本组16例患者基本临床资料完整,包括性别、年龄、就诊症状、治疗方式及预后。检查方法 :全部
引文
[1]Fan M,Lin Y,Liu L.Multiple pulmonary chondroid hamartoma[J].JThorac Oncol,2014,9(7):1053-1054.
[2]Carlsen CJ,Kiaer W.Chondromatous Hamartoma of the Lung[J].Thorax,1950,5(4):283-292.
[3]Carney JA,Sheps SG,Go VLW,et al.The Triad of Gastric Leiomyosarcoma,Functioning Extra-Adrenal Paraganglioma and Pulmonary Chondroma[J].N Engl J Med,1977,296(26):1517-1518.
[4]Basu S,Nandy S,R ajan MG,et al.Chondro id hamar toma presenting as solitar y pulmonar y nodule:results of dual time point(18)F-fluorodeoxyglucose-PET and comparison with(18)F-fluorothymidine PET and histopathology[J].Hell J Nucl Med,2011,14(2):173.
[5]Gregori-Romero MA,Lopez-Gines C,Cerda-Nicolas M,et al.Recombinations of chromosomal bands 10q24,12q14-q15,and14q24 in two cases of pulmonary chondroid hamartoma studied by fluorescence in situ hybridization[J].Cancer Genet Cytogenet,2003,142:153-157.
[6]Carney JA.Carney triad:a syndrome featuring paraganglionic,adrenocortical,and possibly other endocrine tumors[J].J Clin Endocrinol Metab,2009,94:3656-3662.
[7]Sargent EN,Bar nes R A,Schw inn CP.Mult iple pulmonar y fibroleiomyomatous hamartomas.Report of a case and review of the literature[J].Am J Roentgenol Radium Ther Nucl Med,1970,110(4):694.
[8]Domínguez H,Hariri J,Pless S.Multiple pulmonary chondrohamartomas in trachea,bronchi and lung parenchyma.Review of the literature[J].Respir Med,1996,90(2):111.
[9]Li L,Jiang C,Tian R.A pulmonary chondromatous hamartoma resembling multiple metastases in the(18)F-FDG PET/CT scan.[J].Hell J Nucl Med,2016,19(2):176.
[10]廖焕元.肺软骨瘤样错构瘤的CT影像学特点[J].医学信息,2013(9):581-581.
[11]武汉医学院病理学教研室.外科病理学.上册[M].武汉:湖北人民出版社,1978.
[12]姚秀娟,陈祥义,许建秋,等.肺多发性纤维平滑肌瘤型错构瘤一例[J].中华结核和呼吸杂志,2018,41(4):314-315.
[13]Tomà?B,Marek S,Ji?íK,et al.Videothoracoscopic identification of chondromatous hamartoma of the lung[J].Wideochir Inne Tech Maloinwazyjne,2013,8(2):152-157.
[14]Lee YC,Moon JC,Gang SJ,et al.Pulmonary chondroid hamartoma with nontuberculous mycobacterial infection:two case reports[J].Medicine,2015,94(14):e689.
[2]Carlsen CJ,Kiaer W.Chondromatous Hamartoma of the Lung[J].Thorax,1950,5(4):283-292.
[3]Carney JA,Sheps SG,Go VLW,et al.The Triad of Gastric Leiomyosarcoma,Functioning Extra-Adrenal Paraganglioma and Pulmonary Chondroma[J].N Engl J Med,1977,296(26):1517-1518.
[4]Basu S,Nandy S,R ajan MG,et al.Chondro id hamar toma presenting as solitar y pulmonar y nodule:results of dual time point(18)F-fluorodeoxyglucose-PET and comparison with(18)F-fluorothymidine PET and histopathology[J].Hell J Nucl Med,2011,14(2):173.
[5]Gregori-Romero MA,Lopez-Gines C,Cerda-Nicolas M,et al.Recombinations of chromosomal bands 10q24,12q14-q15,and14q24 in two cases of pulmonary chondroid hamartoma studied by fluorescence in situ hybridization[J].Cancer Genet Cytogenet,2003,142:153-157.
[6]Carney JA.Carney triad:a syndrome featuring paraganglionic,adrenocortical,and possibly other endocrine tumors[J].J Clin Endocrinol Metab,2009,94:3656-3662.
[7]Sargent EN,Bar nes R A,Schw inn CP.Mult iple pulmonar y fibroleiomyomatous hamartomas.Report of a case and review of the literature[J].Am J Roentgenol Radium Ther Nucl Med,1970,110(4):694.
[8]Domínguez H,Hariri J,Pless S.Multiple pulmonary chondrohamartomas in trachea,bronchi and lung parenchyma.Review of the literature[J].Respir Med,1996,90(2):111.
[9]Li L,Jiang C,Tian R.A pulmonary chondromatous hamartoma resembling multiple metastases in the(18)F-FDG PET/CT scan.[J].Hell J Nucl Med,2016,19(2):176.
[10]廖焕元.肺软骨瘤样错构瘤的CT影像学特点[J].医学信息,2013(9):581-581.
[11]武汉医学院病理学教研室.外科病理学.上册[M].武汉:湖北人民出版社,1978.
[12]姚秀娟,陈祥义,许建秋,等.肺多发性纤维平滑肌瘤型错构瘤一例[J].中华结核和呼吸杂志,2018,41(4):314-315.
[13]Tomà?B,Marek S,Ji?íK,et al.Videothoracoscopic identification of chondromatous hamartoma of the lung[J].Wideochir Inne Tech Maloinwazyjne,2013,8(2):152-157.
[14]Lee YC,Moon JC,Gang SJ,et al.Pulmonary chondroid hamartoma with nontuberculous mycobacterial infection:two case reports[J].Medicine,2015,94(14):e689.