撒哈拉以南非洲国家(贝宁)心外异位的外科修复。

IF 0.3 Q4 SURGERY
Thoracic and Cardiovascular Surgeon Reports Pub Date : 2025-09-18 eCollection Date: 2025-01-01 DOI:10.1055/a-2698-3658
Abdel Kémal Bori Bata, Désiré Nékoua, Ahmad Ibrahim, Boris Gogan, Eugène Zoumenou
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引用次数: 0

摘要

背景:心异位(EC)是一种非常罕见的先天性异常,预后较差,特别是在资源有限的地区。病例描述:我们报告了一个新生儿患有完全胸椎EC,在出生第5天接受了手术矫正。尽管实现了心脏复位和软组织覆盖,但婴儿在术后72小时死于感染性休克,这反映了在这种情况下面临的重大挑战。结论:该病例强调迫切需要改善产前保健和技术资源,以提高撒哈拉以南非洲复杂先天性异常的结局。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Surgical Repair of Ectopia Cordis in a Sub-Saharan African Country (Benin).

Surgical Repair of Ectopia Cordis in a Sub-Saharan African Country (Benin).

Surgical Repair of Ectopia Cordis in a Sub-Saharan African Country (Benin).

Surgical Repair of Ectopia Cordis in a Sub-Saharan African Country (Benin).

Background: Ectopia cordis (EC) is an exceptionally rare congenital anomaly with a poor prognosis, particularly in resource-limited settings.

Case description: We present a newborn with complete thoracic EC who underwent surgical correction on day 5 of life. Although cardiac repositioning and soft tissue coverage were achieved, the infant died 72 hours postoperatively from septic shock, reflecting the significant challenges faced in such contexts.

Conclusion: This case underscores the urgent need for improved antenatal care and technical resources to enhance outcomes for complex congenital anomalies in sub-Saharan Africa.

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