• 대한방사선기술학회지:방사선기술과학
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• 제27권4호
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• pp.17-21
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• 2004

최근 의학 영상 기술의 발전과 함께 동적 골반 MRI(Pelvic magnetic resonance imaging)가 소개되었고 이러한 기술을 이용하여 동적 MR 배변조영술이 소개되어 환자의 진단에 도움을 주기 위해 사용되고 있다. 처음에 도입 당시에는 탈장(Enterocele)과 방광탈출증(Cystocele) 등을 진단하기 위하여 사용되었지만, 이후 장기의 탈출증(Prolapse), 또는 다른 골반 장기의 이상에 점점 그 유용성이 증명되어 현재는 기능성변비 등 다른 질환에서도 많은 보고가 있다. 본 논고에서는 골반 MRI 및 동적 MR 배변조영술에 대해서 소개하고 앞으로의 임상적 응용에 대한 전망을 살펴보도록 한다. 최근까지도 Pelvic MRI의 결과들은 앙와위(Supine position)에서 골반의 움직임을 관찰하는데 Yang 등은 26명의 골반 기관의 탈출증(Pelvic organ prolapse)을 가진 환자들을 관찰하고 Pubococcygeal line을 해부학적인 지표로 이용하여 좋은 결과를 얻었다고 보고했다. 이들은 Fast gradient recalled acquisition(fast GRASS)을 이용하여, Cystocoele, Prolapse, Enterocoele 그리고 Rectocoele 등을 증상이 없는 대조군과 비교하여 보고하였다. Kruyt 등은 Posterior compartment를 주로 관찰하여 MRI가 Fluoroscopy에 비하여 더 도움이 된다고 보고하였다. Healy 등은 Fast GRASS sequence를 이용하여 변비를 가진 환자와 변실금을 가진 환자, 그리고 증상이 없는 대조군을 대상으로 하여 동적 MRI 검사를 실시하였다. 이들은 변비나 변실금 증상과 관련되어 환자들의 Posterior compartment에 여러 곳에서 Prolapse을 관찰할 수 있었다. 이후 MRI 기술은 Lienemann 등에 의해서 더욱 발전했는데 그는 Fast T2 weighted turbo spin echo 기술을 이용하여 영상을 좀더 세밀하게 얻을 수 있게 되었다. 지금까지의 앙와위에서의 검사로 진단에 한계가 있었던 Intussusception 등의 질환을 Open MR 등의 방법으로 극복할 수 있다면 장래에는 방사선학적 배변조영술을 대체할 수 있는 검사법으로 발전할 수 있을 것으로 생각된다.

• Advances in pediatric surgery
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• 제13권2호
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• pp.127-134
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• 2007

소아 멕켈씨 게실의 가장 흔한 합병증은 장출혈이었고, 장중첩, 장폐쇄, 장천공 등도 있었다. 멕켈씨 게실의 조직검사상 이소성위조직이 가장 많았고, 이소성 췌장조직도 있었다. 소아 급성 복증의 원인으로 멕켈씨 게실에 의한 합병증을 염두에 두어야겠으며, 진단이 불명확한 경우, 복강경을 통한 진단이 도움이 될 수 있을 것이다. 또한 멕켈씨 게실의 경우 복강경하 절제술로 복강경 수술의 장점을 충분히 살릴 수 있을 것으로 사료된다.

• Advances in pediatric surgery
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• 제4권2호
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• pp.110-116
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• 1998

This is a clinical review of 2,191 pediatric surgical patients under the age of 15 years, operated upon at the Division of Pediatric Surgery, Department of Surgery, Chonnam University Hospital from January 1988 to December 1997. The total number of operations in the pediatric age for all specialties were 13,144(13.2 %). The total operations including those performed on adults were 99,555. The most common age group operated upon was under 5 year of age(44.4 %). The number of operations in Division of General Pediatric Surgery were 2,191(16.7 %) out of total 13,144 operations in all pediatric specialties. The patients under 1 year of age in general pediatric surgery was 42.9 %(941/2,191). The most common diseases in neonates were anorectal malformation(20.6 %) and hypertrophic pyloric stenosis(20.3 %). Infants older than neonates most commonly were operated upon for inguinal hernia(32.4 %) and intussusception(19.6 %). The total mortality rate in the neonatal intensive care unit was 31.3 %. Gastroschisis had the highest mortality.

• Pediatric Gastroenterology, Hepatology & Nutrition
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• 제12권1호
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• pp.70-74
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• 2009

저자들은 급성 복통을 주소로 내원한 10세 남아에서 복부 초음파와 복부 전산화단층촬영을 통하여 대망 경색을 진단하였으며 항생제 및 진통제 등의 보존적인 치료로 증상의 완화를 경험하였기에 문헌고찰과 함께 보고하는 바이다.

• Clinical and Experimental Pediatrics
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• 제45권3호
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• pp.406-412
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• 2002

저자들은 Henoch-$Sch{\ddot{o}}nlein$ 자반증에 의한 심한 복통으로 내원한 5년 9개월 남아에서 corticosteroid 투여 도중에 합병된 소장 천공 1례를 경험하였기에 문헌 고찰과 함께 보고하는 바이다.

• Advances in pediatric surgery
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• 제1권1호
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• pp.59-62
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• 1995

Meconium peritonitis is defined as an aseptic, chemical or foreign-body peritonitis caused by spill of meconium in the abdominal cavity related to the prenatal perforation of the intestine. Perforation is usually caused by obstruction from meconium ileus, intestinal atresia, stenosis, volvulus, internal hernia, congenital peritoneal bands, intussusception, or gastroschisis. Less commonly, no evidence of distal obstruction exists. Here, we present two cases of generalized meconium peritonitis of antenatal diagnosis. The first case, detected at 8 months of gestational age, had a perforation of the proximal blind pouch of jejunal atresia, associated with respiratory distress due to severe abdominal distension. This case was successfully treated with resection and anastomosis and brief period of postoperative ventilatory support. The second case had a distal ileal perforation with thick meconium in the terminal ileum. In this case, there was no dilatation of ileum proximal to the perforation site. Resection and anastomosis was performed and postoperative course was uneventful.

• Clinical and Experimental Pediatrics
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• 제54권8호
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• pp.322-328
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• 2011

Nephrotic syndrome (NS) is one of the most common glomerular diseases that affect children. Renal histology reveals the presence of minimal change nephrotic syndrome (MCNS) in more than 80% of these patients. Most patients with MCNS have favorable outcomes without complications. However, a few of these children have lesions of focal segmental glomerulosclerosis, suffer from severe and prolonged proteinuria, and are at high risk for complications. Complications of NS are divided into two categories: disease-associated and drug-related complications. Disease-associated complications include infections (e.g., peritonitis, sepsis, cellulitis, and chicken pox), thromboembolism (e.g., venous thromboembolism and pulmonary embolism), hypovolemic crisis (e.g., abdominal pain, tachycardia, and hypotension), cardiovascular problems (e.g., hyperlipidemia), acute renal failure, anemia, and others (e.g., hypothyroidism, hypocalcemia, bone disease, and intussusception). The main pathomechanism of disease-associated complications originates from the large loss of plasma proteins in the urine of nephrotic children. The majority of children with MCNS who respond to treatment with corticosteroids or cytotoxic agents have smaller and milder complications than those with steroid-resistant NS. Corticosteroids, alkylating agents, cyclosporin A, and mycophenolate mofetil have often been used to treat NS, and these drugs have treatment-related complications. Early detection and appropriate treatment of these complications will improve outcomes for patients with NS.

• Journal of Chest Surgery
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• 제28권2호
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• pp.170-176
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• 1995

Fourty nine patients out of 127 esophageal cancer were managed surgically from January 1986 to December 1991, at the Department of Thoracic and Cardiovascular Surgery, Jeonbuk National University Hospital. Most frequent preoperative symptom was dysphagia and its mean duration was 3.1 months. In histopathologic examination, squamous cell carcinomas were 44 cases [89.8% , and adenocarcinomas 5 [10.2% . The tumor location were the upper esophagus in 6.1%, middle esophagus in 57.2%, lower and cardiac portion of stomach in 36.7%. Involved and metastatic organs, which were detected perioperatively, were celiac lymph nodes in 6 cases, aorta 2, stomach 2, pericardium 2, cervical lymph node 1. The esophagus was resected radically, and the procedures for esophageal replacement were performed with esophagogastrostomy in 45 cases, esophagocologastrostomy 3, and esophagojejunostomy 1. Postoperative complications occurred in 16 cases [hospital morbidity = 32.6% ,anastomotic leak 3, anastomotic stricture 2, respiratory insufficiency 2, hemoperitoneum 1, chylothorax 1, intussusception 1, empyema 1, non-A,non-B hepatitis 1, and mediastinitis 1. Hospital deaths were experienced 3 cases [ hospital mortality = 6.1% . The 6 month, one, two, and five year actuarial survival rates were 85.7%, 71.4%, 57.1%, and 27.9%, respectively. One year survival rates of stages were 100% in stage I, 90.9% in stage IIa, 63.6% in stage IIb, 25.0% in stage III, and 7.2% in stage IV.

• Pediatric Gastroenterology, Hepatology & Nutrition
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• 제22권3호
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• pp.291-297
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• 2019

Bowel ischemia is a life-threatening surgical emergency. We report a case of rapidly progressive bowel necrosis in a previously healthy child without proven mechanical small bowel obstruction. The definite diagnosis was established at the time of an exploratory operation. Of note, imaging studies and even a laparotomy did not reveal any evidence of acute appendicitis or mechanical obstruction such as intussusception or Meckel's diverticulum. During hospitalization, since we could not rule out surgical abdomen after inconclusive image findings, we closely followed the patient and repeated physical examinations carefully. Eventually surgical exploration was performed based on changes in clinical condition, which proved to be the right decision for the patient. We propose that in children with suspected strangulation of small bowel obstruction, especially when imaging findings do not provide a conclusive diagnosis, the timely exploratory surgical approach ought to be chosen based on carefully observed clinical findings and other evaluations.

• Childhood Kidney Diseases
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• 제23권2호
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• pp.128-133
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• 2019

Henoch-$Sch{\ddot{o}}nlein$ purpura (HSP) is a systemic vasculitis characterized by purpura, arthritis, abdominal pain, and nephritis. Gastrointestinal involvement can manifest as pain, intussusception, intestinal bleeding, and intestinal perforation. We report a case of fulminant HSP at an age of eight in 1994, with multiple complications of intra-thoracic bleeding, massive intestinal perforation, nephritis, and various skin rashes. The brisk bleeding findings of intestinal on Technetium-99m-labeled red blood cell scan ($^{99m}Tc$ RBC scan) were well matched to those of the emergency laparotomy and the resected intestine. The patient's abdominal conditions improved gradually but nodular skin eruptions developed newly apart from improving preexisting lower limb rashes and the urine findings continued abnormal, so skin and kidney biopsy were done for the diagnosis. After cyclosporine therapy, skin eruptions and urine findings returned to normal gradually. On a follow-up after 25 years in 2019, the patient is 33-year-old, healthy without any abnormality on blood chemistries and urine examination.