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

IF 1.7 Q2 PEDIATRICS Pediatric health, medicine and therapeutics Pub Date : 2023-01-01 DOI:10.2147/PHMT.S397462
Dawit Seyoum Gebremariam, Asmamaw Miruts, Kibrom Gebreselassie Desta
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Abstract

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.

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孤立的v型胸骨裂-一种罕见的胸壁畸形。
胸骨裂是一种罕见的胸壁异常,由外侧中胚层褶皱未能迁移到中线引起,在胚胎发育早期引起胸壁裂。这可能是一个完全或部分缺陷。它也可以作为一个孤立的异常或与其他综合征相关联。胎儿超声诊断这种缺陷是可能的,但实践较少。出生后,这种缺陷很容易在临床上诊断,因为存在矛盾的胸壁运动。在新生儿和婴儿早期,胸腔的灵活性是最大的,对底层结构的压迫是最小的,这一时期是手术修复的首选时间。我们报告一个39天大的婴儿谁提出孤立的v形胸骨下裂,其手术初步关闭,和术后病程。
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