[1]张艳霞① 孔赤寰 马立霜*.胃镜联合腹腔镜诊治先天性幽门闭锁1例报告[J].中国微创外科杂志,2024,01(5):398-400.
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胃镜联合腹腔镜诊治先天性幽门闭锁1例报告()
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《中国微创外科杂志》[ISSN:1009-6604/CN:11-4526/R]

卷:
01
期数:
2024年5期
页码:
398-400
栏目:
个案报告
出版日期:
2024-05-25

文章信息/Info

作者:
张艳霞① 孔赤寰 马立霜*
（首都儿科研究所附属儿童医院普通(新生儿)外科，北京100020）
文献标志码:
D

参考文献/References:

[1]Mboyo A, Clermidi P, Podevin G, et al. Neonatal gastric outlet obstruction by isolated pyloric atresia, an often forgotten diagnosis. Acta Chir Belg,2016,116(2):89-95.
[2]Kansra M, Raman VS, Kishore K, et al. Congenital pyloric atresianine new cases: Singlecenter experience of the longterm followup and the lessons learnt over a decade. J Pediatr Surg,2018,53(11):2112-2116.
[3]Prasad GR, Rao JVS, Fatima F, et al. Congenital pyloric atresia: Experience with a series of 11 cases and collective review. J Indian Assoc Pediatr Surg,2021,26(6):416-420.
[4]Merrow AC, Frischer JS, Lucky AW. Pyloric atresia with epidermolysis bullosa: fetal MRI diagnosis with postnatal correlation. Pediatr Radiol,2013,43(12):1656-1661.
[5]Khan YA, Zamir N. Missed congenital pyloric atresia with gastric perforation in a neonate. J Neonatal Surg,2012,1(2):32.
[6]Kajal P, Rattan KN, Bhutani N, et al. Congenital pyloric atresia: Early and delayed presentationsA single centre experience of a rare anomaly. Indian J Gastroenterol,2016,35(3):232-235.
[7]孔赤寰,李龙,李颀,等.内镜下治疗先天性幽门前瓣膜三例.中华消化内镜杂志,2016,33(6):399-400.
[8]AlSalem AH, Abdulla MR, Kothari MR, et al. Congenital pyloric atresia, presentation, management, and outcome: a report of 20 cases. J Pediatr Surg,2014,49(7):1078-1082.
[9]Huerta CT, Sundin A, Gilna GP, et al. Laparoscopicassisted open pyloroduodenostomy repair of pyloric atresia in an infant: A rare congenital anomaly. Surg Laparosc Endosc Percutan Tech,2021,32(1):150-152.
[10]Luo C,Yang L,Huang Z,et al.Case report:A case of epidermolysis bullosa complicated with pyloric atresia and a literature review.Front Pediatr,2023,11:1098273.

备注/Memo

备注/Memo:
*通讯作者，Email：malishuang2006@sina.com ①（北京协和医学院研究生院，北京100005）
更新日期/Last Update: 2024-08-06