• Journal of Chest Surgery
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• 제25권7호
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• pp.702-706
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• 1992

Abnormalities of ventral foregut budding have been classified as "Bronchopulmonary Foregut Malformation[BPFM]". Two cases of this unusual malformation are presented. The first case was that of a 48-year-old male with a history of hemoptysis and fever. He had intralobar sequestration, located in the right lower lobe and the posterior segment of the right upper lobe, communicated with the lower esophageal fistula. The sequestrated lobe received its blood supply from anormalous feeding artery from the descending thoracic aorta. The second case was that of a 42-year-old woman with intralobar sequestration that communicated with the lower esophagus. The intralobar sequestration was located in the superior segment of the right lower lobe, and in this case, the abnormal feeding artery could not be found. In both cases, there were no other combined congenital anomalies. They were managed with surgical resection successfully and followed up without any significant complications.lications.

• Archives of Plastic Surgery
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• 제49권1호
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• pp.55-58
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• 2022

In Van der Woude syndrome (VWS), a rare congenital disease, lower lip pits (LLPs) can cause an aesthetically significant deformity. Surgical treatment of LLPs is necessary if they cause recurrent inflammation or aesthetic problems. Intraoperatively, surgeons should keep in mind the possibility of deep extension of the sinus tract and the relative deficiency of the midline in VWS, which increases the risk of lip disfigurement. Herein, we emphasize the importance of using a tissue-preserving technique to improve aesthetic results in VWS patients with a sinus tract.

• 대한수의학회지
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• 제21권2호
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• pp.151-159
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• 1981

An investigation on various causes of milking disturbances resulting from injuries and abnormalities of mammary system were made in 2,179 Holstein cows. To perform this investigation, 69 dairy farms of the suburban area of Seoul city, Gyeonggi-do and Chungnam provinces were andomly selected and subjected. Diagnosis was made by means of inspection and palpation of teat, insertion of teat canula, checking milk machines, anamneses and farm records. This investigation was, actively done from March 1977 to February 1979, The results obtained were summerized as follows; 1. It was found that 446 cows, accounting for 20.48% of 2,179 cows inspected, had supernumerary teats. Among them 53.59% had one, 43.72% had two, 2.47% had three, and 0.22% had four supernumerary teats, respectively. 2. Dry off quarters were found in 158 quarters which turned out to be 1.8% of 8,716 quarters inspected. Among dry off quarters, 62.02% seemed to be caused by mastitis, 30.37% by acquired teat obstructions, and 7.59% by congenital blind teats and glands respectively. 3. Teat sphincter stenosis was found in 154 teats of 50 cows, which represents 1.76% of 8,716 teats and 2.29% of 2,179 cows inspected, respectively. Among 154 teats with teat sphincter stenosis, 138 teats (85.7%) of 33 cows were found to be congenital and revealed highest incidence. 4. Loose sphincter was found in 78 teats of 36 cows, which figure 0.89% of 8,7l6 teats and 1.69% of 2,179 cows inspected, respectively. Among 78 teats with loose sphincter, 52 teats (66.66%) of 13 cows were found to be congenital and revealed highest incidence. 5. Injured teat tip caused by over milking of milk machine, was found in 229 teats of 156 cows, which figure 2.63% of 8,716 teats and 7.15% of 2,179 cows observed, respectively. 6. Other miscellaneous injuries and congenital abnormalities of teats and udders were diagnosed as follows: The teat laceration was found in 34 teats (0.39% of 8,716 teats), fissure of teat skin in 24 teats (0.28% of 8,716 teats), stricture of teat cistern in 21 teats (0.24% of 8,716 teats), teat fistula in 12 teats (0.14% of 8,716 teats), papillomas on testes in 8 teats (0.09% of 8,716 teats). Knothole orifice in 7 teats (0.08% of 8,716 teats), subcutaneous abscess of udder in 5 quarters (0.05% of 8,716 teats), membraneous obstruction of teat cistern in 4 teats (0.05% of 8,716 teats), and congenital short teat in 8 teats (0.09% of 8,716 teats), respectively.

• Journal of Chest Surgery
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• 제34권10호
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• pp.787-791
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• 2001

관상동맥류는 매우 드문 질환으로, 통상적으로 주위 정상 분절보다 내경이 1.5배 이상 초과하여 비정상적으로 확장되어 있는 경우로 정의된다. 유병률은 백인종에서는 2.6%, 동양인에서는 0.25%로, 전자는 약 반수이상이 죽상경화성 관상동맥질환과 관련되어 있으나, 후자는 70% 정도가 비폐쇄성 동맥류와 관련되어 있는 것으로 보고 된 바 있다. 관상동맥루 또한 매우 드문 질환으로, 10년간 실시한 심혈관조영촬영술에서 단지 0.2% 만이 발견되었다고 보고된 바 있다. 증상은 없을 수도 있고, 무증상적 심잡음, 운동시 호흡 곤란, 피로감, 울혈성 심부전 등으로 나타날 수 있다. 주침범 관상동맥은 우관상동맥(56%), 좌관상동맥(36%) 순이고, 원위부 연결 부위는 우심실(39%), 우심방(33%), 폐동맥(20%)으로 보고된 바 있다. 저자들의 경우 단순흉부사진과 흉부전산화단층촬영상 종격동 종양이 의심되어 좌측전측방 개흉술로 종양제거를 시도했다. 그러나 종양은 좌실실에서 기원하고, 수술 중 실시한 거대종괴(6$\times$6$\times$6cm)내 바늘흡입검사 상 박동성의 동맥혈이 분출하여서, 심장 박동 중에 제거하는 것이 매우 위험하다고 판단되어 수술을 계속 진행하지 않았다. 개흉술 4일 후 실시한 심혈관조영술 상 첫사선관상동맥(1st diagonal artery)에서 혈류를 받는 심장종양이 의심되었고, 상행대동맥에서 총폐동맥간으로 연결되는 관상동맥루가 우연히 발견되었다. 정중흉골절개술 후, 체외순환 하에서 종양 제거술과 관상동맥루 결찰술을 성공적으로 실시하였다. 수술후 병리 조직소견상 심장종양이 아닌 관상 동맥류로 판명되었으며 수술 후 합병증 없이 경쾌 퇴원하였다.

• Advances in pediatric surgery
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• 제1권2호
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• pp.149-161
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• 1995

국내에서 처음으로 기관식도기형에 관하여 대한소아외과 학회 회원을 대상으로 조사하였다. 본 연구는 두 부분으로 구성되어 있었는데 하나는 최근 3년간 출생한 기관식도기형의 등록된 자료를 분석하여 국내의 기관식도기형의 현황 즉 발병율 처치 및 치료 결과등에 관한 총체적인 경향을 외국과 비교 분석하여 우리 자료와 구미 보고와의 차별성 및 유사성을 분석하고저 했으며, 다른 하나는 질문서(questionnaires) 분석을 토대로 11차 대한소아외과학회 학술대회에서 토의된 내용을 기초로 회원들의 식도기형의 진단 치료, 술후 관리, 합병증 등에 대한 경험과 의견을 종합하여 고안을 작성하였다.

• Journal of Chest Surgery
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• 제16권2호
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• pp.231-242
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• 1983

A clinical study was performed on 75 cases of the esophageal cancer and benign esophageal diseases experienced at Department of thoracic & cardiovascular surgery, School of Medicine, Keimyung University during 3 year period from 1978 to 1982. Of 75 cases of the surgical esophageal diseases, there were 35 patients of the esophageal cancer. 17 patients of benign esophageal stenosis, 10 patients of esophageal perforation, 4 patients of diverticulum. 3 patients of achalasia, 2 patients of congenital T-E fistula, one of upper esophageal web, one of esophageal foreign body, one of leiomyoma and patient of hemangioma. First, esophageal carcinoma was more frequent in men than in women by a ratio of five to one, and the peak incidence occurred in the 5th to 6th decade. Dysphagia was the most common symptom in 88.6 percent of our cases. The tumor was located mostly in the middle & the lower one third [91.4%]. The histological diagnosis was made in 35 cases. The squamous cell carcinoma was the most common [82.9%] and the rest was the adenocarcinoma in the lower one third [17.1%]. Thirty-five cases were operated and resection was feasible in the twenty-five patients [71.4%] with 2 cases of hospital mortality [5.7%]. All but two of the esophageal stenosis were caused by corrosive esophagitis and ages ranged from 7 to 70 years with average age of 32 years. Corrective operations were performed on 17 patients of esophageal stenosis of whom 12 patients had esophagocologastrostomy, 3 patients esophagogastrostomy and in non-corrosive esophageal stenosis one case and esophagoplasty and another case had release of external compression. There was one complication of stenosis of the esophageal perforation were traumatic in five cases, empyema in three cases, caustics in one case and postemetic in one case. 10 patients of the esophageal perforation underwent operation: primary closure in 5 cases, two staged colon interposition in 2, esophagogastrostomy in 1 and closed thoracotomy in 2 cases There were 2 complications of leakage of anastomosis sites in postoperative period. 4 patients of traction type of diverticulum underwent diverticulectomy & 3 patients of achalasia underwent modified Heller`s operation. 2 patients of congenital esophageal atresia had distal tracheoesophageal fistula & underwent one staged operation with the results of one death caused by pneumonia. Upper esophageal web had divulsion through the esophagoscope and foreign body in upper esophagus was removed through cervical esophagotomy. One case of leiomyoma in esophagus had esophagectomy and reconstruction with right colon. And one case of hemangioma in esophagus had esophagectomy & esophagogastrostomy.

• 대한소아치과학회지
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• 제27권3호
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• pp.388-393
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• 2000

순 구개열(cleft lip and palate)은 구강악안면 영역에서 가장 빈번하게 발생하는 선천성 기형 중 하나로 유전적, 환경적 요인에 의해 발생된다. 순 구개열 환자는 입술, 코 등의 기형을 보이며 치과적 문제점으로, 이환측 측절치는 결손되어 있거나 과잉치가 존재하고 형태적 이상을 보이는 경우가 많고, 맹출하지 못하거나 이소맹출을 하게된다. 이른 시기에 수행된 수술의 반흔조직(scar tissue)으로 인하여 상악골 성장의 장애가 발생되어 흔히 골격성 III급 부정교합이 야기되기 쉬우며, 섭식장애와 발음장애를 보이기도 한다. 이러한 복잡한 문제로 인하여 여러 분야의 전문가들로부터 다양한 관리가 필요하다. 순/구개열(cleft lip and alveolus only)은 악안면 영역에 제한적으로 영향을 미친다. 비이환측은 전방으로 회전되어 수평피개가 증가되고, 이환측은 내측으로 회전되어 견치부에서 end to end 관계, 혹은 반대교합을 보인다. 순/구개열 수술은 이와 같은 문제점 등을 개선시키기 위한 것이며, 상악골의 전후방적 성장에는 큰 영향을 미치지 않는 것으로 보고되고 있다. 본 증례는 좌측에 순/구개열을 가진 5세 3개월의 여아로 생후 3개월 및 3세에 두 번의 구순열 봉합 수술을 받았으며, 상악 좌측 유측절치와 영구측절치가 결손되어 있었고, 다발성 우식증 및 비구누공(oroantral fistula)이 존재하였으며, 골격성 3급 부정교합을 보였다. 그러나 본 증례가 지니고 있는 골격성 III급 부정교합은 구순열 수술후의 반흔조직에 의한 것은 아닌 것으로 판단되었으며, 환자의 기능과 심미성을 회복하기 위하여 혼합치열기 동안 공간관리(space supervision) 및 악기능 장치 (functional regulator)를 이용한 골격성 부정교합을 치료하였으며, 영구치열기 동안 고정성 교정치료를 시행한 후 보철 치료를 시행하여 비구누공을 key and keyway attachment와 Konus crown을 이용한 가철성 obturator로 폐쇄하여 양호한 결과를 보였다.

• Archives of Plastic Surgery
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• 제40권6호
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• pp.766-772
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• 2013

Background Hypospadias is the most common congenital malformation of the male urinary tract, wherein the urethral opening is located proximal to the normal site. Tubularized incised-plate urethroplasty reconstruction, and its efficacy, remains controversial due to the high recurrence rate. This study aimed to evaluate the results of dartos fascia-reinforced flap surgery in hypospadias patients with previous operative complications. Methods Nine patients (mean age, 12 years) who had previous one- or two-stage repair with TIP urethroplasty and suffered from urethrocutaneous fistulas or fissures as complications, underwent dartos fascia-reinforced flap surgery in our clinic between January 2010 and December 2012. The mean postoperative follow-up period was 6 months. Results Among the 9 patients, 7 had complete correction. In all the patients, the maximum uroflow angle was > $45^{\circ}$. No patient complained of an unnatural urinating position. The patients and parents gave very high satisfaction scores (4.7 points) with regard to the appearance of the outer genitalia. Conclusion The dartos fascia-reinforced flap could be a useful and reliable option for complications of hypospadias repair or fissure with the prepuce preserved, given that histological aspects vary and that the possibility of recurrence in the glanular region is high.

• Advances in pediatric surgery
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• 제13권1호
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• pp.37-44
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• 2007

A vitelline duct (VD) anomaly is a relatively common congenital abnormality of the umbilical area. The anomalies include patent vitelline duct (PVD), cyst, fistula or sinus. The incidence is approximately 2% of the populations, but development of symptoms is rare. Recently, we experienced two cases; PVD accompanied by a small omphalocele and intestinal volvulus due to mesenteric band between Meckel's diverticulum and the mesentery. Thereafter,we evaluated the data of vitelline duct anomalies for 27 years. From 1980 to 2006, 18 cases of VD anomalies were reviewed based on the hospital records retrospectively. There were 15 boys and 3 girls and age ranged from 2 days to 15 years. Among the 18 cases, 15 cases were symptomatic and consisted of Meckel's diverticulum (10 cases), PVD (4 cases) and umbilical polyp (1 case). Three asymptomatic cases of Meckel's diverticulum were found incidentally were and were observed without resection. Ten cases of Meckel's diverticulum were presented with intestinal bleedings (4 cases), intestinal obstructions (5 cases) and perforation (1 case). Wedge resections and segmental resections of ileum were performed in 8 patients and 2 patients, respectively. Postoperative complications were adhesive ileus (1 case) and wound seroma (1 case). Small omphaloceles were accompanied in two of 4 PVD patients. There was 1 small omphalocele case which was accompanied by a prolapse of ileum. In summary, VD anomalies were more common in male and more than half of them were found in patients less than 1 year of age. PVD was diagnosed most frequently in neonates. Meckel's diverticulum presented with intestinal obstruction more frequently than bleeding.

• Advances in pediatric surgery
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• 제10권2호
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• pp.87-91
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• 2004

As prenatal ultrasonography becomes popular, the number of prenatal diagnosis of congenital surgical diseases is also increasing. To evaluate the impact of antenatal ultrasonography on outcome the mortality rate in neonatal surgical emergencies was studied. The authors retrospectively reviewed 281 patients (congenital diaphragmatic hernia: 44, tracheoesophageal fistula: 78, intestinal atresia: 98, omphalocele: 28 and gastroschisis: 33 who had been managed at Seoul National University Childrens Hospital, from January 1991 to December 2000. The patients were divided into two groups; group A (1991 to 1995; 139 patients) and group B (1996 to 2000; 142 patients). These two groups were subdivided into prenatally diagnosed subgroup and postnatally diagnosed subgroup. We analyzed the changes of prenatal diagnosis rate, total mortality rate, and mortality rate of subgroups. Prenatal diagnosis rate was increased significantly in group B (Group A: 24.5 % and Group B: 45.1 %). Total mortality rate of group A was 21.6 %, and that of group B was 10.6 %, showing a significant decrease in group B. However, in both group A and B, when compared antenatally diagnosed subgroup with postnatally diagnosed subgroup, the mortality rate was lower in postnatally diagnosed subgroups but statistically not significant. The authors conclude that although prenatal diagnosis rate has been increased, prenatal diagnosis itself has not resulted in significant improvement in outcome.