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"Intestinal obstruction"

Case Report

[English]
Transmesenteric internal hernia through a mesenteric defect presenting as small bowel obstruction in a 15-year-old boy: a case report and literature review
Jinyoung Park
Received June 30, 2026  Accepted July 29, 2026  Published online October 16, 2026  
DOI: https://doi.org/10.13029/aps.2026.00122    [Epub ahead of print]
Internal hernia is an uncommon cause of small bowel obstruction, especially in children and adolescents with no history of abdominal surgery. Among its subtypes, transmesenteric hernia through a mesenteric defect is rare but clinically important because it can lead to closed-loop obstruction, bowel ischemia, and intestinal strangulation. Early diagnosis and timely surgical treatment are therefore essential. A previously healthy 15-year-old boy was transferred to our emergency department with left upper quadrant abdominal pain and vomiting that had persisted for 2 days. His vital signs were stable on arrival, and physical examination showed only mild left upper quadrant tenderness, with no abdominal distension. Abdominal computed tomography revealed two transition points in the mid-abdomen and dilatation of the left-sided small bowel loops, findings suggestive of closed-loop obstruction. Emergency laparoscopic exploration showed two segments of small bowel herniated through a defect in the jejunal mesentery. Although laparoscopic reduction was attempted first, marked bowel dilatation and the small size of the mesenteric defect prevented safe reduction. The procedure was therefore converted to open surgery through a periumbilical incision. The incarcerated bowel loops were carefully reduced, and the mesenteric defect was closed with interrupted sutures. The patient developed mild postoperative ileus, which resolved with conservative treatment. At the 1-year follow-up, he remained well, with no recurrence or postoperative sequelae. Transmesenteric internal hernia caused by a mesenteric defect should be considered in adolescents with small bowel obstruction, even when they have no history of abdominal surgery. Prompt surgical exploration and closure of the mesenteric defect may prevent bowel ischemia and strangulation and support favorable outcomes.
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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.

Citations

Citations to this article as recorded by  
  • Laparoscopic Appendectomy in Children with Perforated Appendicitis
    So-Hyun Nam, Dae-Yeon Kim, Seong-Chul Kim, In-Koo Kim
    Journal of the Korean Surgical Society.2009; 76(1): 47.     CrossRef
  • 1,023 View
  • 6 Download
  • 1 Crossref

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.

Citations

Citations to this article as recorded by  
  • A Transmesenteric Hernia in a Child: Gangrene of a Long Segment of Small Bowel through a Large Mesenteric Defect
    Chan Yong Park, Jung Chul Kim, Soo Jin Na Choi, Shin Kon Kim
    The Korean Journal of Gastroenterology.2009; 53(5): 320.     CrossRef
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  • 3 Download
  • 1 Crossref

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.

Citations

Citations to this article as recorded by  
  • Primary anastomosis in jejunoileal atresia: A qualitative synthesis of outcomes, surgical techniques, and decision-making factors
    Amani N. Alansari, Fatima Mansour Elfeituri, Mousa Mohamed, Mohammed A. Mahmoud, Hanan Youssif, Marwa Messaoud, Ayman Albaghdady
    Asian Journal of Surgery.2026; 49(6): 3231.     CrossRef
  • Fetal MRI: abdominal cystic lesions
    David García Castellanos, Manuel Recio Rodríguez, Lucía Sanabria Greciano, Alejandra Aguado del Hoyo, Alejandro Díaz Moreno, Julia López Alcolea, Carolina Sampietro, Vicente Martínez de Vega
    Insights into Imaging.2026;[Epub]     CrossRef
  • Design and validation of a low-cost modular simulator for training in neonatal laparotomy and jejunoileal atresia repair
    Ryan Yeung, Daniel S. Kwon, Abdullah Mashat, Ajay Banga, Rachel Livergant, Roger Tam, Shahrzad Joharifard
    Journal of Pediatric Surgery.2026; 61(1): 162521.     CrossRef
  • Fetal Hydrops, Meconium Peritonitis, and Distal Ileal Atresia in a Neonate with a Homozygous Fanconi Anemia FANCG Splice Variant: A Case Report
    Kanithi Ravishankar, Kambham Rishika
    Newborn.2026; 5(2): 109.     CrossRef
  • Atresia of the Transverse Colon (Grosfeld Type IIIa) Diagnosed at Seven Days of Life: A Case Report
    Urias J Hernandez Lopez, Pastor A Thomas Olivares, Adriana P Redondo Rada, Vanessa P Quiñones Cantillo, Vicky G Gomez Montes
    Cureus.2026;[Epub]     CrossRef
  • A rare combination of gastroschisis, jejunal atresia, colonic atresia, and midgut malrotation in a newborn: a case report and literature review
    Layth J.M. Saada, Malak Ismael Marei, Tareq Fiqyat, Yaman Abu Sarrees, Amir Atawneh, Jamil Saada
    International Journal of Surgery Case Reports.2026;[Epub]     CrossRef
  • Frequency of Types of Jejunoileal Atresia among Neonates Presenting With Intestinal Obstruction
    Fatima Majid, Sana Aslam, Muhammad Anwar, Misbah Abdul Ghaffar, Yasir Ahmed, Fareeha Nazar
    Pakistan Journal of Health Sciences.2025; : 102.     CrossRef
  • Minimally invasive single-port video-assisted surgery for the treatment of neonatal intestinal atresia: tertiary care centre experience
    Paulina Vargova, Carolina Corona-Bellostas, Ricardo Escartin-Villacampa, Yurema Gonzalez-Ruiz, Rafael Fernandez-Atuan, Andrea Santinno-Tenorio, Paolo Bragagnini-Rodriguez
    Journal of Pediatric Endoscopic Surgery.2025; 7(1): 7.     CrossRef
  • 13,451 View
  • 253 Download
  • 8 Crossref

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.

Citations

Citations to this article as recorded by  
  • Cecal Duplication Cyst Presenting With Hematochezia
    Serina Beydoun, James W. Davis, Namir Al-Ansari
    ACG Case Reports Journal.2025; 12(3): e01640.     CrossRef
  • 983 View
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  • 1 Crossref
[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.

Citations

Citations to this article as recorded by  
  • Gallstone Obstruction in Roux-en-Y Hepaticojejunostomy: An Unusual Challenge After Liver Transplant for Biliary Atresia
    Sydney R. Donohue, Apoorva K. Chandar, Kai Zhao, Anthony B. Post
    ACG Case Reports Journal.2025;[Epub]     CrossRef
  • 954 View
  • 5 Download
  • 1 Crossref