우측 횡격막 탈장증
Right Congenital Posterolateral Diaphragmatic Hernia
차선욱, 정재희, 송영택,
소속 상세정보
차선욱 ( Cha Seon-Wook )
가톨릭대학교 의과대학 외과학교실
정재희 ( Chung Jae-Hee )
가톨릭대학교 의과대학 외과학교실
송영택 ( Song Young-Tack )
가톨릭대학교 의과대학 외과학교실
KMID : 0371320020630040350
Abstract
Congenital right posterolateral diaphragmatic hernia is rare. Moreover, cases of delayed presentation are extremely rare. We experienced two cases of right posterolateral diaphragmatic hernia. One case was a 1 day old male neonate with cyanosis. He
was
diagnosed as a congenital right posterolateral diaphragmatic hernia by chest X-ray and repaired primarily through trans-abdominal approach. There was a 54 ㎝ defective area at the right posterolateral diaphragm. The right lobe of the liver, gall
bladder, small intestine and right colon were herniated though the defect into the thoracic cavity. The patient was supported by mechanical ventilation for 1 month and was discharged without complication on the 41st day. The other case was an
11-month
male infant with dyspnea, cough and seizure. He was diagnosed with delayed presentation of congenital right posterolateral diaphragmatic hernia by chest X-ray and repaired primarily through transabdominal approach. Almost all of the small intestine
and
right colon were herniated through a 54 ㎝ sized posterolateral defect in the right diaphragm. He didn’t need postoperative ventilatory support and was discharged without complications on the ninth day.
키워드
우측 횡격막 탈장; Right congenital posterolateral diaphragmatic hernia;
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