Bochdalek疝和部分膈肌发育不全:带蒂肋间肌瓣和补片修复一例年轻镰状细胞病患者。

Pub Date : 2021-12-23 eCollection Date: 2021-10-01 DOI:10.1055/s-0041-1740628
Klein Dantis, Devendra Kumar Rathore, Nilesh Gupta, Subrata Kumar Singha
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引用次数: 0

摘要

先天性Bochdalek疝(BH)在成人是罕见的,有一个不寻常的表现。它们局限于儿科年龄组,活产发生率为1:3 000。它很少持续无症状直到成年。胸、腹或胸腹入路手术修复是相关膈发育不全的膈重建的首选治疗方法。迄今为止,仅有10例BH伴部分膈肌发育不全的报道,我们讨论了在文献中未报道的年轻成人镰状细胞病中BH的罕见性、不寻常的表现和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Bochdalek Hernia and Partial Diaphragmatic Agenesis: Pedicled Intercostal Muscle Flap and Mesh Repair in a Young Adult with Sickle Cell Disease.

Bochdalek Hernia and Partial Diaphragmatic Agenesis: Pedicled Intercostal Muscle Flap and Mesh Repair in a Young Adult with Sickle Cell Disease.

Bochdalek Hernia and Partial Diaphragmatic Agenesis: Pedicled Intercostal Muscle Flap and Mesh Repair in a Young Adult with Sickle Cell Disease.

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Bochdalek Hernia and Partial Diaphragmatic Agenesis: Pedicled Intercostal Muscle Flap and Mesh Repair in a Young Adult with Sickle Cell Disease.
Congenital Bochdalek hernia (BH) in an adult is rare and has an unusual presentation. They are confined to the pediatric age group with an incidence of 1:3,000 live births. It rarely persists asymptomatic until adulthood. Surgical repair by thoracic, abdominal, or thoraco-abdominal approach is the treatment of choice with diaphragmatic reconstruction in associated diaphragmatic agenesis. With only 10 cases of BH with partial diaphragmatic agenesis reported to date, we discuss the rarity, unusual presentation, and management of BH in a young adult with sickle cell disease that has not been reported in the literature.
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