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박진영,장수일,Park, Jin-Young,Chang, Soo-Il 대한소아외과학회 1997 소아외과 Vol.3 No.1
A clinical review was done of 31 children with blunt liver injury who were admitted to the Department of Surgery, Kyungpook National University Hospital between 1981 and 1990. Seventeen of the 31 children required laparotomy(11 primary repairs, 4 lobectomies, 2 segmentectomies). There were two deaths after laparotomy, one due to associated severe head injury and another due to multiorgan failure. The remaining 14 children, who were hemodynamically stable after initial resuscitation and who did not have signs of other associated intraabdominal injuries, were managed by nonoperative treatment. Patients were observed in a pediatric intensive care unit for at least 48 hours with repeated abdominal clinical evaluations, laboratory studies, and monitoring of vital signs. The hospital courses in all cases were uneventful and there were no late complication. A follow-up computed tomography of 7 patients showed resolution of the injury in all. The authors believe that, for children with blunt liver injuries, nonoperative management is safe and appropriate if carried out under careful continuous surgical observation in a pediatric intensive care unit.
박동원,장수일,Park, Dong-Weon,Chang, Soo-Il 대한소아외과학회 1997 소아외과 Vol.3 No.2
Appendiceal perforation is uncommon in the neonate. Diess reported the first case in 1908. Approximately 111 additional cases have been reported since that time. However, with exclusion of neonatal appendicitis associated with inguinal or umbilical hernias, necrotizing enterocolitis, meconium plug, and Hirschsprung's disease, there are only 36 cases of primary neonatal appendicitis. We treated a 12 days old boy with perforation of the appendix. The infant was 3000 g at birth and had a normal spontaneous vaginal delivary at 35 weeks of gestation. The mother was 31-year-old and had premature rupture of membrane. After normal feeding for the first 5 days of life, the infant had emesis of undigested milk, decreased activity and jaundice. The baby was admitted to the Pediatrics. Progressive abdominal distension, fever, decreased activity, and vomitting developed over the next six days. Erect abdominal radiography showed pneumoperitoneum. At exploratory laparotomy, a $0.8{\times}0.6$ cm sized perforation was noted at antime-senteric border of midportion of the appendix. Trasmural inflammation and the presence of ganglion cells were noticed on histology.
십이지장 무공증을 동반한 복부 내장 전위증 - 1예 보고-
박진영,최병호,장수일,Park, Jin-Young,Choe, Byung-Ho,Chang, Soo-Il 대한소아외과학회 2009 소아외과 Vol.15 No.1
Situs inversus abdominis is a rare congenital condition commonly associated with serious cardiac and splenic malformations. The importance of recognizing the presence of situs inversus abdominis preoperatively is emphasized by the fact that the surgical incision is placed on the incorrect side of the abdomen. A 6 day-old girl was referred to our hospital because of bile stained vomiting. A plain radiography of abdomen and chest showed the heart to be normal position and a reversed "double-bubble" picture with no other gas shadow in the rest of the abdomen. Abdominal computed tomography scan revealed situs inversus with the stomach and polysplenia on the right side and the liver on the left side. A laparotomy confirmed the diagnosis of situs inversus with duodenal atresia. The obstruction was bypassed by constructing a side-to-side duodenoduodenostomy. The postoperative course was uneventful.
이상규,박동원,장수일,Lee, Sang-Kyu,Park, Dong-Weon,Chang, Soo-Il 대한소아외과학회 1998 소아외과 Vol.4 No.1
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. Although diaphragmatic eventration in newborn infants is generally regarded as a rare condition, the need for accurate diagnosis and appropriate intervention according to the etiological factors is well known. Recently the authors experienced five consecutive cases of diaphragmatic eventration below the age of two months(one to 55 days) requiring surgery. All were in males, and were left sided. Respiratory symptoms were present in 4 patients, and one patient showed inability to gain weight. Diaphragms were elevated to the level of the third to fifth intercostal spaces. Diaphragmatic plication through the abdomen gave excellent results. There was no postoperative mortality.