全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
华西医学  2013 

先天性囊性腺瘤样畸形

DOI: 10.7507/1002-0179.20130157, PP. 489-493

Keywords: 先天性囊性腺瘤样畸形,错构瘤,手术治疗

Full-Text   Cite this paper   Add to My Lib

Abstract:

目的 全面介绍先天性囊性腺瘤样畸形(CCAM)其可能的病因,临床、病理特点及诊断手段,循证探讨针对CCAM的治疗方法及预后。方法 对我院2011年11月收治的1例罕见的CCAM患者的临床资料进行分析,并对相关文献进行复习。结果 患者数次误诊后最终诊断为CCAM,予手术治疗后痊愈,随访1年无复发。结论 CCAM是一种少见的、非遗传性的、错构瘤样的肺发育异常,为一种良性的肺部畸形,其特点是局部肺终末呼吸性细支气管过度生长。CCAM多通过产前影像学检查、活组织检查或术后病检诊断。手术为治愈该病的最根本、最重要措施。

References

[1]  [ 1 ] Ch’In K, Tang M. Congenital adenomatoid malformation of one lobe of a lung with general anasarca[J]. Arch Pathol (Chic), 1949, 48(3): 221-229.
[2]  [ 2 ] Laberge J, Flageole H, Pugash D, et al. Outcome of the prenatally diagnosed congenital cystic adenomatoid lung malformation: a Canadian experience[J]. Fetal Diagn Ther, 2001, 16(3): 178-186.
[3]  [ 3 ] Khan N, Jones M, Greaves M. Congenital cystic adenomatoid malformation of an entire lung in a 33-year-old man: a case report and review of the literature[J]. Br J Radiol, 2008, 81(971): 276-278.
[4]  [ 4 ] Cass DL, Quinn TM, Yang EY, et al. Increased cell proliferation and decreased apoptosis characterize congenital cystic adenomatoid malformation of the lung[J]. J Pediatr Surg, 1998, 33(7): 1043-1047.
[5]  [ 5 ] Berrocal T, Madrid C, Novo S, et al. Congenital Anomalies of the Tracheobronchial Tree, Lung, and Mediastinum: Embryology, Radiology, and Pathology1[J]. Radiographics, 2004, 24(1): 17-17.
[6]  [ 6 ] 刘键平, 常晓燕, 陈杰, 等. 肺先天性囊性腺瘤样畸形 4 例临床病理分析[J]. 诊断病理学杂志, 2006, 13(4): 247-249.
[7]  [ 7 ] Stocker JT, Madewell JE, Drake RM. Congenital cystic adenomatoid malformation of the lung: classification and morphologic spectrum[J]. Hum Pathol, 1977, 8(2): 155-171.
[8]  [ 8 ] Lakhoo K. Management of congenital cystic adenomatous malformations of the lung[J]. Arch Dis Child Fetal Neonatal Ed, 2009, 94(1): 73-76.
[9]  [ 9 ] Patz Jr EF, Müller NL, Swensen SJ, et al. Congenital cystic adenomatoid malformation in adults: CT findings[J]. J Comput Assist Tomogr, 1995, 19(3): 361-364.
[10]   Stanton M, Njere I, Ade-Ajayi N, et al. Systematic review and meta-analysis of the postnatal management of congenital cystic lung lesions[J]. J Pediatr Surg, 2009, 44(5): 1027-1033.
[11]   Nasr A, Bass J. Thoracoscopic vs open resection of congenital lung lesions: a meta-analysis[J]. J Pediatr Surg, 2012, 47(5): 857-861.
[12]   Colon N, Schlegel C, Pietsch J, et al. Congenital lung anomalies: can we postpone resection[J]. J Pediatr Surg, 2012, 47(1): 87-92.
[13]   Nagata K, Masumoto K, Tesiba R, et al. Outcome and treatment in an antenatally diagnosed congenital cystic adenomatoid malformation of the lung[J]. Pediatr Surg Int, 2009, 25(9): 753-757.
[14]   Conforti A, Aloi I, Trucchi A, et al. Asymptomatic congenital cystic adenomatoid malformation of the lung: Is it time to operate[J]. J Thorac Cardiovasc Surg, 2009, 138(4): 826-830.
[15]   Sueyoshi R, Okazaki T, Urushihara N, et al. Managing prenatally diagnosed asymptomatic congenital cystic adenomatoid malformation[J]. Pediatr Surg Int, 2008, 24(10): 1111-1115.
[16]   Wong A, Vieten D, Singh S, et al. Long-term outcome of asymptomatic patients with congenital cystic adenomatoid malformation[J]. Pediatr Surg Int, 2006, 25(6): 479-485.
[17]   Kim YT, Kim JS, Park JD, et al. Treatment of congenital cystic adenomatoid malformation-does resection in the early postnatal period increase surgical risk[J]. Eur Cardiothorac Surg, 2005, 27(4): 658-661.
[18]   Khosa JK, Leong SL, Borzi PA. Congenital cystic adenomatoid malformation of the lung: indications and timing of surgery[J]. Pediatr Surg Int, 2004, 20(7): 505-508.
[19]   Aziz D, Langer JC, Tuuha SE, et al. Perinatally diagnosed asymptomatic congenital cystic adenomatoid malformation: to resect or not[J]. J Pediatr Surg, 2004, 39(3): 329-333.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133