Thoracoscopic repair for late‐presenting congenital diaphragmatic hernia with thoracic kidney in a child

Author:

Fukuhara Masahiro12ORCID,Kaisyakuji Yushi2,Sato Tomoe2,Izaki Tomoko2

Affiliation:

1. Department of Pediatric Surgery, Faculty of Medical Sciences Kyushu University Fukuoka Japan

2. Department of Pediatric Surgery Oita Prefectural Hospital Oita City Japan

Abstract

AbstractCongenital diaphragmatic hernia (CDH) with a hernia sac and thoracic kidney is a very rare congenital anomaly. Recently, the usefulness of endoscopic surgery for CDH has been reported. We herein report a patient who underwent thoracoscopic repair of CDH with a hernia sac and thoracic kidney. A 7‐year‐old boy was referred to our hospital due to a diagnosis of CDH without clinical symptoms. Computed tomography showed herniation of the intestine into the left thorax and left‐sided thoracic kidney. The key points of operation are resection of the hernia sac and identification of the suturable diaphragm under the presence of the thoracic kidney. In the present case, after repositioning the kidney to the subdiaphragmatic area completely, the border of the diaphragmatic rim was clearly visualized. Good visibility allowed resection of the hernia sac without damaging the phrenic nerve and closure of the diaphragmatic defect.

Publisher

Wiley

Subject

General Medicine

Reference9 articles.

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