Neonate with congenital pulmonary airway malformation concurrent with enteric duplication cyst: a case report of a rare anomaly

被引:0
|
作者
Krishnan, Amit [1 ]
Schmoke, Nicholas [2 ]
Nemeh, Christopher [2 ]
Wu, Yeu Sanz [2 ]
Duron, Vincent [2 ,3 ]
机构
[1] New York Med Coll, Westchester Med Ctr, Valhalla, NY 10595 USA
[2] Columbia Univ, New York Presbyterian Morgan Stanley Childrens Hos, Div Pediat Surg, Dept Surg,Vagelos Coll Phys & Surg, New York, NY 10032 USA
[3] Morgan Stanly Childrens Hosp, Div Pediat Surg, 3959 Broadway,CHN 215, New York, NY 10032 USA
来源
JOURNAL OF SURGICAL CASE REPORTS | 2023年 / 2023卷 / 09期
关键词
neonate; duplication cyst; congenital pulmonary airway malformation; laparoscopic; thoracoscopic; pediatric surgery; INFANTS;
D O I
10.1093/jscr/rjad502
中图分类号
R61 [外科手术学];
学科分类号
摘要
A congenital pulmonary airway malformation (CPAM) occurring concurrently with an enteric duplication cyst is a rare anomaly. Definitive management for both abnormalities is usually surgical resection. We present the uncommon case of a neonate with a CPAM and ileal duplication cyst, including pre-natal and post-natal workup. The patient was brought to the operating room for laparoscopic duplication cyst excision at 3 months of age. The patient returned to the operating room for a thoracoscopic right lower lobectomy at five months of age. This case presents a rare congenital anomaly with the concurrent presentation of a CPAM and enteric duplication cyst, with both being successfully excised minimally invasively.
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页数:3
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