Isolated V-Shaped Sternal Cleft-A Rare Chest Wall Malformation

被引:0
作者
Gebremariam, Dawit Seyoum [1 ,4 ]
Miruts, Asmamaw [2 ]
Desta, Kibrom Gebreselassie [3 ]
机构
[1] Mekelle Univ, Coll Hlth Sci, Dept Pediat & Child Hlth, Mekelle, Tigray, Ethiopia
[2] Mekelle Univ, Coll Hlth Sci, Dept Surg, Pediat Surg Unit, Mekelle, Tigray, Ethiopia
[3] Mekelle Univ, Coll Hlth Sci, Dept Surg, Cardiothorac Unit, Mekelle, Tigray, Ethiopia
[4] Mekelle Univ, Coll Hlth Sci, Dept Pediat & Child Hlth, POB 1871, Mekelle 1871, Tigray, Ethiopia
关键词
sternal cleft; surgery; congenital anomaly; complication;
D O I
10.2147/PHMT.S397462
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Sternal cleft is a rare chest wall anomaly resulting from a failure of the lateral mesodermal folds to migrate to the midline, causing a cleft in the early stage of embryological development. This can be a complete or partial defect. It can also occur as an isolated anomaly or in association with other syndromes. Fetal sonographic diagnosis of this defect is possible, but less practiced. After birth, this defect can be easily diagnosed clinically because of the presence of paradoxical chest wall movement. The flexibility of the thorax is maximal and compression of the underlying structures is minimal during the neonatal and early infancy period, and this period is the preferred time for surgical repair. We report a 39-day-old infant who presented with an isolated V-shaped inferior sternal cleft, its surgical primary closure, and postoperative course.
引用
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页码:81 / 87
页数:7
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