• Journal of Chest Surgery
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• 제17권1호
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• pp.144-149
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• 1984

Diaphragmatic eventration is a rare condition in primary diaphragmatic diseases and is found rarely in clinical experience. Diaphragmatic eventration means abnormally high position of diaphragm, which is caused acquired, paralytic or congenital, nonparalytic etiologic origins. This report is presented a symptomatic diaphragmatic eventration of 50 years old woman, who had complained coughing and left chest pain since I year ago prior to admission in Kosin Medical College, Gospel Hospital. A patient who had established accurate diagnosis at pre-operative period. There had been post-operative course uneventfully.

• Journal of Chest Surgery
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• 제20권4호
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• pp.855-858
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• 1987

Eventration of the diaphragm is a rare anomaly, the cause of which still is not understand completely. Recently we were experienced two cases of diaphragmatic eventration which were successfully treated with surgical diaphragmatic plication at the department of thoracic and cardiovascular surgery, college of medicine, chosun university. Specific complication were not noticed after surgical repair of diaphragmatic eventration with good results.

• Journal of Chest Surgery
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• 제20권3호
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• pp.630-634
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• 1987

Anomalies of the diaphragm, particularly eventration, are not encountered frequently in clinical practices. Diaphragmatic eventration is generally accepted as an anomaly high position of part or all of the diaphragm, usually associated with a marked decrease in muscle fibers and a membranous appearance of the abnormal area. We experienced 3 cases of the congenital diaphragmatic eventration at the department of the thoracic and cardiovascular surgery, Maryknoll Hospital, which were treated successfully.

• Journal of Chest Surgery
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• 제26권9호
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• pp.730-734
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• 1993

Three neonates with congenital diaphragmatic eventration underwent intrathoracic operation had marked improvements in symptoms postoperatively. Two were one day of ages, one was 1 month of age, and they were all female and had other congenital abnormalities of lung hypoplasia, cleft palate, nasal polyps and neonatal hepatitis. The right diaphragm was more affected than left as 2:1. The repair for diaphragmatic eventration was performed successfully by plication of remnant diaphragm, and there were no complications postoperatively.

• Journal of Chest Surgery
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• 제32권2호
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• pp.201-205
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• 1999

횡격막성 내장전위는 드문 질환이며 선천적인 원인에 의한다. 저자들은 기존에 좌측 횡격막성 내장전위가 있던 상태에서 교통사고로 인한 우측 횡격막 마비가 동반되어 호흡부전에 빠진 환자에 대한 수술을 시행하였다. 본 례는 국내외 문헌에 아직 보고된 례가 없는 매우 희귀한 경우로서 횡격막 주름성형술을 시행하여 좋은 결과를 얻었기에 보고하는 바이다.

• Journal of Veterinary Science
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• 제25권2호
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• pp.19.1-19.6
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• 2024

A 2-year-old spayed female British Shorthair cat presented with an increased frequency and duration of cough since infant period. Based on radiographic, ultrasonographic, and computed tomography findings, peritoneopericardial diaphragmatic hernia was considered so that repair surgery was planned. During celiotomy, lax diaphragm was identified instead of defect. Transabdominal diaphragmatic plication was performed to resolve lax diaphragm and to prevent recurrence by overlapping relatively normal part of diaphragm. Diagnosed with diaphragmatic eventration postoperatively, the cat showed improvement in clinical signs and imaging results. Transabdominal diaphragmatic plication is a suitable treatment; the patient maintained normally during a 14-month follow-up period.

• Pediatric Gastroenterology, Hepatology & Nutrition
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• 제9권1호
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• pp.92-97
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• 2006

선천성 횡격막 내장탈출은 드문 질환으로 산전 초음파로 횡격막 헤르니아와 감별하는 것은 쉽지 않다. 선천성 횡격막 내장탈출과 횡격막 헤르니아의 예후가 다르고 수술적 접근 방식이 다를 수 있어 정확한 감별 진단이 필요하다. 저자들은 산전 초음파 검사에서 선천성 횡격막 헤르니아로 진단되었으나 수술 시에 선천성 횡격막 내장탈출로 진단된 두 증례의 후향적 분석을 통하여 비록 출생 직후의 단순 흉부 사진으로는 두 질환의 감별 진단이 어려웠으나 연속적인 단순흉부사진에서 뚜렷하게 드러나는 병변 측 횡격막을 확인하는 경험을 하였다. 따라서 산전 초음파 검사에서 횡격막 헤르니아로 진단되었다 하더라도 출생 이후에 촬영한 연속적인 단순흉부사진의 주의 깊은 판독을 통한 재평가를 강조하고자 한다.

• Advances in pediatric surgery
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• 제6권1호
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• pp.60-63
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• 2000

Spontaneous rupture of the eventrated diaphragm is not common. The authors report a case of spontaneous rupture of the congenital diaphragmatic eventration. An 8 year-old girl with right congenital diaphragmatic eventration and nephrotic syndrome was seen in emergency room because of severe abdominal pain and vomiting. She had intermittent abdominal pain for 1 year. Plain chest X-ray and ultrasonography showed entrapped bowels in the right thoracic area. Exploratory laparotomy revealed a ruptured right eventration. THE displaced abdominal viscera were repositioned into the abdominal cavity and the ruptured diaphragm was trimmed and plicated. The postoperative course was uneventful. Only one case of spontaneous rupture of eventrated diaphragmatic has been reported in the English literature.

• Journal of Chest Surgery
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• 제15권3호
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• pp.290-294
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• 1982

Diaphragmatic eventration is a rare disease, congenital or acquired, high or elevated position of one leaf of the diaphragm muscle, as a result of paralysis, aplasia or atrophy of varying degree of the muscle fibers of the affected side but with no break in the continuity of the muscle. We experienced 3 cases of the diaphragmetic eventration at the department of thoracic surgery, C.A.F.G.H., from 1980 to 1982, which were treated successfully. Among three cases, one case combinded with hamartoma of the ipsilateral lung. Specific complications were not noticed after surgical repair of diaphramatic eventration with good result.

• Advances in pediatric surgery
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• 제4권1호
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• pp.67-73
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• 1998

신생아 및 영아에서의 횡격막 이완증은 일반적으로 드문 질환으로 인식되어 있지만 이에 대한 정확한 진단과 적절한 원인별 처치의 필요성은 널리 알려진 사실이다. 최근 저자 등은 5 례의 선천성 횡격막 이완증을 경험할 수 있었고, 전 례 모두 수술이 적응되었다. 전 례 모두 생후 2개월 미만의 영아였고 모두 남아였다. 이완 부위는 전 예에서 좌측 횡격막이었다. 증상은 3례에서 호흡기 증상이 있었고 소화기계 증상은 없었으며 나머지 1례에서는 체중 증가불능 이 외는 무증상이었다. 전 예에서 방사선학적 변화가 저명하였고, 횡격막의 절정은 제 3에서 제 5늑간에 달하였다. 수술 술기로 저자 등은 경복부 접근 방법에 의한 횡격막 습벽 봉합술을 선호하였으며 수술 결과는 임상적으로나 방사선학적으로 우수하였다.