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Double H-type tracheoesophageal fistula
被引:0
作者:
Tanny, Sharman P. Tan
[1
,2
,3
]
King, Sebastian K.
[1
,2
,3
]
Omari, Taher I.
[4
]
Teague, Warwick J.
[1
,2
,3
]
机构:
[1] Royal Childrens Hosp, Dept Paediat Surg, 50 Flemington Rd, Parkville, Vic 3052, Australia
[2] Murdoch Childrens Res Inst, F Douglas Stephens Surg Res Grp, 50 Flemington Rd, Parkville, Vic 3052, Australia
[3] Univ Melbourne, Dept Paediat, Parkville, Vic 3052, Australia
[4] Flinders Univ S Australia, Dept Human Physiol, Sturt Rd, Bedford Pk, SA 5042, Australia
基金:
英国医学研究理事会;
关键词:
Tracheoesophageal fistula;
Congenital;
Case report;
OUTCOMES;
ATRESIA;
D O I:
10.1016/j.epsc.2020.101662
中图分类号:
R72 [儿科学];
学科分类号:
100202 ;
摘要:
Congenital 'isolated' tracheoesophageal fistula (TEF) is a rare variant of esophageal atresia, also termed H-type TEF. Even rarer is a double H-type TEF. Here, we report a two-week-old female, with double H-type TEF - one identified pre-operatively, the other during surgery. Pre-operative laryngotracheobronchoscopy (LTB) with guidewire cannulation is considered key to definitive TEF repair, to aid in both pre- and intra-operative identification of the fistula(e). In our experience, only one H-type TEF was identified at the planned pre-operative LTB, with the second H-type fistula identified at the time of cervical dissection. Both fistulae were repaired during the same operation, via cervical approach. This represents the first reported case of a double H-type TEF, repaired primarily via a single cervical incision.
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