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VACTERL综合征中的支气管异常。

Bronchial anomalies in VACTERL association.

作者信息

Kanu Adaobi, Tegay David, Scriven Richard

机构信息

Department of Pediatrics, Texas Tech University, HSC, Lubbock, Texas, USA.

出版信息

Pediatr Pulmonol. 2008 Sep;43(9):930-2. doi: 10.1002/ppul.20827.

DOI:10.1002/ppul.20827
PMID:18671276
Abstract

VACTERL association is an acronym made of associated defects including vertebral anomalies, anal atresia, cardiac, tracheal-esophageal fistula, and renal/radial limb anomalies. Tracheal bronchus is a condition characterized by ectopic location of the right upper lobe bronchus at the mid to distal trachea. This condition is associated with congenital anomalies and has been reported in one previous case of VACTERL. We report another infant with VACTERL presenting with respiratory complications due to presence of tracheal bronchus. She also had a narrowed segment of her right main stem bronchus.

摘要

VACTERL综合征是一个首字母缩略词,代表一系列相关缺陷,包括脊柱异常、肛门闭锁、心脏、气管食管瘘以及肾脏/桡骨肢体异常。气管支气管是一种以上叶右支气管异位至气管中下段为特征的病症。该病症与先天性异常相关,此前曾在1例VACTERL综合征病例中被报道。我们报告了另一例患有VACTERL综合征的婴儿,因气管支气管的存在而出现呼吸并发症。她的右主支气管也有一段狭窄。

相似文献

1
Bronchial anomalies in VACTERL association.VACTERL综合征中的支气管异常。
Pediatr Pulmonol. 2008 Sep;43(9):930-2. doi: 10.1002/ppul.20827.
2
VACTERL (vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, cardiac defects, renal and limb anomalies) association: disease spectrum in 25 patients ascertained for their upper limb involvement.VACTERL(椎体缺陷、肛门闭锁、气管食管瘘伴食管闭锁、心脏缺陷、肾脏和肢体异常)联合症:25 例上肢受累患者的疾病谱。
J Pediatr. 2014 Mar;164(3):458-62.e1-2. doi: 10.1016/j.jpeds.2013.09.033. Epub 2013 Nov 7.
3
[Vater or Vacterl syndrome (author's transl)].法特或VACTERL综合征(作者译)
Klin Padiatr. 1976 Jul;188(4):328-37.
4
Report of a girl with vacterl syndrome and right pulmonary agenesis.一名患有VACTERL综合征及右肺发育不全女孩的病例报告。
Genet Couns. 2009;20(4):379-83.
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Prenatal diagnosis of VACTERL association: a case report.VACTERL 综合征的产前诊断:一例报告
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VACTERL associations in children undergoing surgery for esophageal atresia and anorectal malformations: Implications for pediatric surgeons.接受食管闭锁和肛门直肠畸形手术的儿童中的VACTERL综合征:对小儿外科医生的启示
J Pediatr Surg. 2015 Aug;50(8):1245-50. doi: 10.1016/j.jpedsurg.2015.02.049. Epub 2015 Mar 10.
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VACTERL association: a new case with biotinidase deficiency and annular pancreas.VACTERL 协会:一例伴生物素酶缺乏和环状胰腺的新病例。
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Computed tomography and upper gastrointestinal series findings of esophageal bronchi in infants.婴儿食管支气管的计算机断层扫描和上消化道造影检查结果
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Tracheal agenesis and associated malformations: a comparison with tracheoesophageal fistula and the VACTERL association.气管发育不全及相关畸形:与气管食管瘘和VACTERL综合征的比较
Am J Med Genet. 1985 May;21(1):21-38. doi: 10.1002/ajmg.1320210104.
10
Non-VACTERL-type anomalies are frequent in patients with esophageal atresia/tracheo-esophageal fistula and full or partial VACTERL association.非VACTERL型异常在食管闭锁/气管食管瘘及完全或部分VACTERL综合征患者中很常见。
Birth Defects Res A Clin Mol Teratol. 2008 Feb;82(2):92-7. doi: 10.1002/bdra.20437.

引用本文的文献

1
Case Report: Esophageal Bronchus in a Neonate, With Image, Histological, and Molecular Analysis.病例报告:新生儿食管支气管,附影像学、组织学及分子分析
Front Pediatr. 2021 Jul 9;9:707822. doi: 10.3389/fped.2021.707822. eCollection 2021.
2
VACTERL association complicated with multiple airway abnormalities: A case report.
Medicine (Baltimore). 2019 Oct;98(42):e17413. doi: 10.1097/MD.0000000000017413.
3
Esophageal lung with rare associated vascular and anorectal malformations.伴有罕见相关血管和肛肠畸形的食管肺。
Radiol Case Rep. 2018 Feb 28;13(2):444-448. doi: 10.1016/j.radcr.2018.01.029. eCollection 2018 Apr.
4
Congenital trifurcation of the trachea.先天性气管三叉。
European J Pediatr Surg Rep. 2014 Jun;2(1):35-7. doi: 10.1055/s-0033-1353367. Epub 2013 Sep 9.
5
A case of bilateral tracheal bronchus: report of a rare association in multidetector computed tomography bronchoscopy.一例双侧气管支气管:多排螺旋计算机断层扫描支气管镜检查中罕见关联的报告。
Surg Radiol Anat. 2015 Aug;37(6):693-6. doi: 10.1007/s00276-014-1383-6. Epub 2014 Nov 6.
6
Tracheal trifurcation associated with esophageal atresia.气管三叉与食管闭锁相关。
APSP J Case Rep. 2010 Jul;1(2):14. Epub 2010 Dec 1.
7
VACTERL/VATER Association.VACTERL/VATER 联合征。
Orphanet J Rare Dis. 2011 Aug 16;6:56. doi: 10.1186/1750-1172-6-56.