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"Intestinal obstruction"

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"Intestinal obstruction"

Original Articles

[English]
Early Experience of Laparoscopic Adhesiolysis in Children with Postoperative Intestinal Obstruction
Jeongwoo Lee, Eunyoung Jung, Woo-Hyun Park, Soon-Ok Choi
J Korean Assoc Pediatr Surg 2013;19(1):32-38.   Published online June 28, 2013
DOI: https://doi.org/10.13029/jkaps.2013.19.1.32

The purpose of this study is to analyze the early experience of the laparoscopic adhesiolysis for the intestinal obstruction due to postoperative adhesion. Seven patients were included in this study. The median age of those patients was 13, and there were 3 males and 4 females. Previous diagnosis and surgical procedure were various in seven cases, including small bowel resection with tapering enteroplasty, Boix-Ochoa fundopl ication, Ladd's procedure with appendectomy, mesenteric tumor resection with small bowel anastomosis, ileocecal resection and anastomosis, primary gastric repair, and both high ligation. A successful laparoscopic adhesiolysis was performed in one who had high ligation for inguinal hernia and had a single band adhesion. Six out of 7 (86%) cases needed to convert open surgery due to multiple and dense type of adhesion. In conclusion, laparoscopic approach with postoperative small bowel adhesion seems safe. However, it might be prudently considered because of high rates of conversion in children.

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[English]
Mechanical Intestinal Obstruction after Appendectomy for Perforated Appendicitis in Children
Ki Myung Moon, Dae Yeon Kim, Seong Chul Kim, In Koo Kim
J Korean Assoc Pediatr Surg 2004;10(2):123-126.   Published online December 31, 2004
DOI: https://doi.org/10.13029/jkaps.2004.10.2.123

Intestinal obstruction secondary to intraabdominal adhesion is a well-known postoperative complication occurring after appendectomy. The aim of this study was to measure the incidence and clinical manifestations of mechanical intestinal obstruction after appendectomy for perforated appendicitis. We reviewed all of the children (age <16 years) who had been treated for appendicitis at Asan Medical Center between January 1996 and December 2001. Inclusion criterion included either gross or microscopic evidence of appendiceal perforation. Exclusion criteria were interval appendectomy, and patients immune compromised by chemotherapy. Associations of intestinal obstruction with age, sex, operation time, and use of peritoneal drains were analyzed. Four hundred and sixty two open appendectomies for appendicitis were performed at our department. One hundred and seventeen children were treated for perforated appendicitis (78 boys, 39 girls). The mean age was 8.9 years (range 1.5 to 14.8 years). There were no deaths. Eight patients were readmitted due to intestinal obstruction, but there was no readmission due to intestinal obstruction in patients with non-perforated appendicitis. The interval between appendectomy and intestinal obstruction varied from 12 days to 2 year 7 months. Four patients needed laparotomies. In three of four, only adhesiolysis was performed. One child needed small bowel resection combined with adhesiolysis. There was no significant association between age or sex and the development of intestinal obstruction. This was no association with operative time or use of peritoneal drain. Patients who required appendectomy for perforated appendicitis have a higher incidence of postoperative intestinal obstruction than those with nonperforated appendicitis. For the patients with perforated appendicitis, careful operative procedures as well as pre and postoperative managements are required to reduce adhesions and subsequent bowel obstruction.

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Case Reports

[English]
Segmental Dilatation of Ileum Combined with Colonic Duplication: A Case Report
Seok Joo Han, Seung Min Kim, Soegu Son, Hogeun Kim, Jai Eok Kim, Eui Ho Hwang
J Korean Assoc Pediatr Surg 1998;4(2):166-171.   Published online December 31, 1998
DOI: https://doi.org/10.13029/jkaps.1998.4.2.166

Segmental dilatation of small intestine is a rare form of the congenital intestinal anomaly. Many other congenital anomalies have been reported in these patients, but to our knowledge, the association with colonic duplication has not been reported in literatures. We report a case of segmental dilatation of distal ileum associated with colonic duplication. The main clinical and pathogenic aspects are discussed, and the literatures were reviewed.

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[English]
Transmesenteric Hernia
Seong-Chul Kim, In-Koo Kim
J Korean Assoc Pediatr Surg 1996;2(2):148-150.   Published online December 31, 1996
DOI: https://doi.org/10.13029/jkaps.1996.2.2.148

Transmesenteric hernia, a type of internal hernias, is a rare cause of intestinal obstruction. This intraperitoneal hernia has no sac and is formed by protrusion of a loop of bowel through an aperture in the mesentery. Incarceration leads to intestinal obstruction and subsequently, strangulation and gangrene of varing lengths of intestine. This is a case report of 4-year-old girl with transmesenteric herniation of the terminal ileum through a defect in its own mesentery. Strangulation of the affected bowel necessitates resection and primary anastomosis with repair of mesenteric defect. The postoperative course was uneventful. Acute intestinal obstruction in the absence of an external hernia and with no history of a previous surgical procedure suggests the possibility of an internal hernia, especially if the patient has a history of chronic intermittent abdominal distress.

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Review Article

[English]
Jejunoileal atresia (JIA) is a rare congenital disorder in newborns leading to intestinal obstruction, necessitating urgent surgery. A delay in diagnosis can result in severe complications like sepsis, bowel perforation, and even death. Over the years, improvements in neonatal care, surgical techniques, and nutrition have led to a marked decrease in mortality rates for JIA patients. While the exact cause remains uncertain, it is thought to result from an ischemic insult during later in utero. JIA is categorized into 4 types, detailing the structure and implications of each type. Clinically, mothers may exhibit polyhydramnios, and infants usually present with symptoms like bilious vomiting and abdominal distension. A significant percentage of affected infants do not pass meconium within the first day of life. Diagnosis is commonly through abdominal radiographs, with some cases requiring contrast enemas. Once diagnosed, immediate surgery is advised, with the primary goal to restore intestinal function and length. Nowadays, the survival rate for JIA patients exceeds 90%. This improvement is attributed to a better understanding of the condition, advancements in surgical techniques, and the introduction of total parenteral nutrition. The prognosis varies, with short bowel syndrome being a significant factor determining the outcome. Short bowel syndrome’s prognosis depends on the remaining small bowel length, the ileocecal valve’s presence, and dependence on long-term nutrition. In conclusion, the treatment and prognosis for JIA have seen substantial improvements due to advances in medical care. Early diagnosis and intervention are crucial. While many patients lead a normal life, those with complications like short bowel syndrome may require long-term care. Future efforts should emphasize refining surgical techniques, gaining a deeper understanding of JIA, and enhancing postoperative care. There's also a need for more research into JIA’s genetics and etiology.
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Case Reports

[English]
Caecal Duplication Cyst in an Infant: A Rare Presentation
Reddy, Manasa , Solanki, Shailesh , Menon, Prema , Samujh, Ram
Adv Pediatr Surg 2023;29(1):45-48.
DOI: https://doi.org/10.13029/aps.2023.29.1.45
Caecal duplication cysts (DCs) are rare anomalies and presentation varies according to size, site, the mucosal lining of the cyst, and age of the patient. The rarity of the condition and varied clinical presentation makes it difficult to diagnose preoperatively. A high index of suspicion and intraoperative examination of the whole bowel is essential to localize intraluminal DC. We herein describe a case of an intraluminal caecal DC in an infant along with its presentation, management, and review of pertinent literature.
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[English]
Surgically Treated Gallstone Ileus 22 Years After Kasai Portoenterostomy: A Case Report
Gang, Sujin , Youn, Joong Kee , Kim, Hyun-Young
Adv Pediatr Surg 2022;28(1):21-25.
DOI: https://doi.org/10.13029/aps.2022.28.1.21
Gallstone ileus occurs when there is a fistula between the gallbladder and the small intestine, by which the gallstone reaches the small bowel and thereby inducing bowel obstruction. This condition is very rare in the overall population, accounting for only 0.1–5%. It is also very rare in the pediatric population and in the patients who undergo Kasai operation as well. Worldwide, only two cases have been reported. Gallstone production may be facilitated under certain circumstances, and migrated stone induces ileus. Diagnosis is usually done by imaging studies such as abdominal ultrasonography and computed tomogram (CT). Surgical removal of stone is decisive treatment. The 22-year-old female patient with a history of Kasai operation at age of 1 month visited emergency department for abdominal pain. The most reasonable impression was the acute exacerbation of the chronic cholangitis, but it was improved soon after intravenous antibiotics treatment. At the same time, mechanical ileus was diagnosed and exacerbated during admission. CT was done to find out the cause. Small bowel obstruction by a round material was observed. By considering its clinical course and the imaging, the material was suspected to be gallstone. The patient underwent enterolithotomy under general anesthesia. She was fully recovered from gallstone ileus after stone removal. There has been no recurrence of ileus nor cholangitis. When a patient with a history of Kasai portoenterostomy complains mechanical ileus, the clinician need to allow for gallstone ileus referring patient’s history and medical condition which promotes to induce stone formation.
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