양측성 부신 신경아세포종

허영수,이희섭,Huh, Young-Soo,Lee, Hee-Sub 대한소아외과학회 1995 소아외과 Vol.1 No.1

Neuroblastoma is the most common solid malignancy in childhood. However, a neuroblastoma presenting as bilateral and multifocal is very rare. A male newborn weighing 2.7 kg was born by normal vaginal delivery at 39 weeks' gestation to a 27-year-old mother who had a normal pregnancy. He was in good condition at birth but presented palpable masses in the both upper abdomen and both side of the neck. Ultrasound examination showed the lesions to be $3{\times}3cm$ sized calcified mass in right suprarenal area and $5{\times}3cm$ sized homogenous mass in left suprarenal area. The abdominal mass was also examined by computed tomography with similar findings. With the impression of bilateral neuroblastoma or metastatic spread, the laparotomy was performed on the 13th day of life. Frozen section of biopsy of the left neck mass was obtained, which showed neuroblastoma. Intraoperative findings revealed bilateral adrenal masses which were distinct and anatomically separate. Bilateral adrenalectomy was accomplished and the initial postoperative course was uneventful. The patient was discharged for hopeless and expired at age 45 days. We present bilateral adrenal neuroblastoma considered to be simultaneous occurrence rather than metastases from one site to another.

영아 비후성 유문 협착증의 임상적 분석

허영수,임명국,김규락,Huh, Young-Soo,Lim, Myeung-Kook,Kim, Kyu-Rak 대한소아외과학회 1998 소아외과 Vol.4 No.1

1990년 1월부터 1997년 7월까지 최근 만 7년 7개월간 영남대학교 의과대학 외과에서 영아 비후성 유문협착증으로 수술받은 환아 64명을 대상으로 임상 분석하여 다음과 같은 결론을 얻었다. 성별 발생 빈도는 남아 56례, 여아 8례로 남아에서 7배 호발하였으며, 내원시 연령은 생후 2주에서 8주 사이가 81%가 가장 많았다. 입원시 체중 백분위수은 전례에서 50백분위수 미만이었고, 총 64례 중 미숙아 3례(4.7 %), 저체중아 2례(7.8 %) 이었으며, 형제 중 발생순위는초산아가 37례(57.8 %)로 가장 많았으며 모유를 수유한 경우가 31례(48.4%), 우유를 수유한 경우가 18례(28.1 %)로 모유를 수유한 경우에서 많은 발생빈도를 보였다. 증상발현시기는 생후 2주에서 4주 사이가 23례(35.9 %)로 가장 많았다. 임상증상으로는 무담즙성 분출성구토가 가장 중요한 증상으로 64례 전 예에서 나타났고 이학적 소견상 초진시 19례(29.7 %)에서 우상복부 종괴가 촉지되었고 16례(25.0 %)에서 가시성 위 유동파가 있었으며 5례(7.8 %)에서 황달을 볼 수 있었으며 혈중전해질의 변화는 저 염소혈증 26례(40.6%), 저칼륨혈증 14례(21.9 %)에서 관찰되었다. 타 병원에서 상부위장관조영술 시행후 전원되었던 4례를 제외한 나머지 60례에서 시행한 복부초음파상 종괴크거의 평균치는 유문근두께 6.3 mm, 유문직경 12.3 mm, 유문관길이 17.8 mm로 측정되었으며, IHPS의 가장 중요한 초음파상 진단적 척도의 기준인 유문근두께가 4mm이상인 경우는 47례(78.3 %), 5 mm 이상인 경우는 41례(68.3 %)로 관찰되었다. 동반기형은 총64례 중 12례(18.8 %)에서 13개의 기형이 관찰되었다. 전례에서 Fredet-Ramstedt씨 유문근절개술을 시행하였고 술후 합병증으로 창상감염이 3례에서 나타났으며, 총 64례 중 13례 (20.3 %)에서 간헐적인 구토증을 호소하였으나 경구투여의 조절로 대부분이 1주이내에 자연 소실되었다. Infantile hypertrophic pyloric stensosis(IHPS) occurs in three of 1000 live births, and is a major cause of nonbilious vomiting of early infancy. It's etiology and pathogenesis however are still obscure. The operation of pyloromyotomy described by Ramstedt in 1912 remains the standard treatment. From January 1990 to July 1997, 64 infants with IHPS were treated at the Department of Pediatric Sursery, Yeungnam University Hospital. The ratio of male to female was 7:1, and the most prevalent age ranged from 2 weeks to 8 weeks(81.2 %) of age. Fifty-seven infants were first born (57.8 percent). The body weight of all patients at admission was below the 50 percentile. Age of onset of symptoms was between 2 and 4weeks of age in 23 cases(35.9 %). All infants had a history of nonbilious vomting, generally projectile in nature. Hypokalemia was noted in 14 cases(21.9 %) and hypochloremia in 26 cases(40.6 %). In the preoperative ultrasonography, the average muscle thickness, diameter, and length of the pylorus were 6.3 mm, 12.3 mm, and 17.8 mm. A total of 13 associated anomalies were noted in 12 patients. All cases were treated with Fredet-Ramstedt pyloromyotomy. Postoperative wound infection occured in 3 cases. Thirteen cases(20.3 %) presented intermittent nonprojectile vomiting after operation. With control of oral intake vomiting subsided within one week in 63 patients, and in thirteen days in another.

진성 비장 낭종 3예

허영수,강수환,윤성수,Huh, Young-Soo,Kang, Su-Hwan,Yun, Sung-Su 대한소아외과학회 1999 소아외과 Vol.5 No.2

Splenic cysts are uncommon and classified as either primary(true) or secondary(pseudo-) depending on the presence or absence of a true epithelial lining. True cysts (epidermoid cyst) of the spleen are very rare. Three cases of splenic cysts in childhood were treated at the Yeungnam University Hospital in the last eleven years(1989-1999). Two of patients were girls. The ages at diagnosis were 7, 12 and 15 years. Abdominal ultrasonography and computerized tomography were utilized for the diagnosis. Radionuclide scanning was performed in one patient. Surgical resection(one partial splenectomy and two total splenectomies) was performed. The sizes of cysts were 4, 6.5 and gem in maximum demension.

췌모세포종 2예

허영수,하정옥,장선모,이정훈,Huh, Young-Soo,Hah, Jeong-Ok,Jang, Seon-Mo,Lee, Jung-Hoon 대한소아외과학회 2000 소아외과 Vol.6 No.2

Pancreatoblastoma is uncommon in children and is exceedingly rare in adults. Prognosis is good if the tumor is removed prior to metastasis. Complete tumor resection is the most important factor for long survival. We report two cases of pancreatoblastoma in 4 and 7 years old girls. Palpable abdominal mass was accidentally found by their parents. Abdominal CT scan showed a huge retroperitoneal mass of unknown origin in one case and a mass involving the pancreas in the other case. At laparotomy, well encapsulated tumor mass($10{\times}10$ cm in maximum dimension) was noted in the body of pancreas in one case, and in the tail of pancreas in the other case( $8{\times}7$ cm). We resected the tumor and preserved the spleen in both cases. Histological examination revealed that the tumors were pancreatoblastoma. Patients received postoperative chemotherapy with 6 cycles of cisplatinum, adriamycin, ifosfamide and etoposide and are alive in good condition 19 months and 17 months after operation.

출혈성 메켈게실의 진단 및 치료

허영수,김범별,윤정훈,곽동민,Huh, Young-Soo,Kim, Bum-Ryul,Yun, Jung-Hoon,Kwack, Dong-Min 대한소아외과학회 2001 소아외과 Vol.7 No.1

The major complications of Meckel's diverticulum (MD) are bleeding, intestinal obstruction, infection, umbilical fistula and perforation. Although the relative incidences vary between authors, bleeding is the most common complication in children. The aim of our study is to show the symptomatic guideline for the diagnosis of the bleeding MD. Eight cases with bleeding MD which were operated upon at the department of Pediatric Surgery, Yeungnam University Hospital from April 1985 to April 2001 were reviewed. Half of the patients were under 2 years of age and all patient s we re male. All patients were preoperatively diagnosed by previous history of intestinal bleeding (melena, hematochezia) and 99mTc pertechnetate MD scan. Segmental resection and end-to-end anastomosis was performed in 6 patients and diverticulectomy in 2 patients. Heterotropic gastric mucosa was found in 6 patients. Postoperative complication was not observed in any cases. In conclusion, in any male children with obscure intestinal bleeding, especially less than 2 years of age, bleeding MD must be suspected. It seems to us that 99mTc pertechnetate MD scan is a useful tool to diagnose bleeding MD.

영아에서 발생한 췌도모세포증의 외과적 치료 1예

허영수,채상철,나목찬,김미진,Huh, Young-Soo,Chai, Sang-Chul,Nah, Mok-Chan,Kim, Mi-Jin 대한소아외과학회 1995 소아외과 Vol.1 No.2

Nesidioblastosis in one of the causes of hyperinsulinemic hypoglysemia in infancy. The most important goal of treatment for persistent hypoglycemia is the prevention of permanent brain damage. The early surgical management is satisfactory to this goal in nesidioblastosis and maintains normal blood sugar level without administration of drugs or supplement of sugar postoperatively in many cases. We experienced a female infant of 3 months old who has suffered from persistent hypoglysemia due to hyperinsulinism and was suspected nesidioblastosis for its cause clinically. She underwent 95% distal pancreatectomy. The histologic findings of nesidioblastosis was confirmed postoperatively. No postoperative complication was occured and her blood sugar levels were maintained within normal range without medical treatment.

신생아에서 게실간막대에 의한 장폐쇄증 1예

허영수(Young Soo Huh),전용성(Yong Sung Jeon),최경찬(Kyung Chan Choi) 대한외과학회 1996 Annals of Surgical Treatment and Research Vol.50 No.6

장폐쇄를 동반한 혈관내피종 1예

허영수(Young Soo Huh),김창식(Chang Sig Kim),최경찬(Kyung Chan Choi),최원희(Won Hee Choi) 대한외과학회 1996 Annals of Surgical Treatment and Research Vol.50 No.6

소아에서 발생한 후복막 지방모세포종 1예

허영수(Young Soo Huh),송기환(Ki Whan Song),김영철(Young Chul Kim),박성규(Sung Kyu Park) 대한외과학회 1999 Annals of Surgical Treatment and Research Vol.56 No.2

회장 중복에 의한 장 출혈 1예

허영수(Young Soo Huh),권오수(Oh Soo Kwun),강수환(Soo Hwan Kang) 대한외과학회 1999 Annals of Surgical Treatment and Research Vol.56 No.3