Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Colonic volvulus (CV) is a rare but potentially life-threatening condition with unclear etiopathogenesis. To date, less than 80 pediatric cases have been described. Hirschsprung's disease (HD) is associated with CV in 17% of cases, representing a significant risk factor. Non-HD CV is an even more complex entity. The aim of this study is to describe a series of patients with CV to accentuate some peculiar aspects of this disease. We performed a retrospective study (period: 2012-2021) collecting information of patients with CV. Data analyzed included: demographics, medical history, presenting symptoms and radiological and surgical details. Eleven patients (12.5 ± 2.8 years; 7F/4M) had CV (eight sigmoid, two transverse colon, one total colon). Five patients had associated anomalies and three had HD. A two-step approach with volvulus endoscopic/radiological detorsion followed by intestinal resection was attempted in eight cases (one endoscopic approach failed). Three patients required surgery at admission. At follow-up, two patients developed recurrent intestinal obstruction, one of whom also had anastomotic stenosis. Colonic volvulus is a challenging condition that requires prompt patient care. A missed diagnosis could lead to severe complications. The evaluation of the patient should include a careful histological examination (searching for HD and alpha-actin deficiency), immunologic and metabolic screening, neurological tests and detection of chronic intestinal pseudo-obstruction (CIPO). Lifelong follow-up is mandatory for the early recognition and treatment of progressive diseases involving the proximal gastrointestinal tract.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8625683PMC
http://dx.doi.org/10.3390/children8110982DOI Listing

Publication Analysis

Top Keywords

colonic volvulus
12
challenging condition
8
patients
6
volvulus children
4
children surgical
4
surgical management
4
management challenging
4
condition colonic
4
volvulus rare
4
rare life-threatening
4

Similar Publications

Sigmoid volvulus and uterine torsion are both rare and challenging conditions in pregnancy, and the coexistence of these conditions is particularly difficult to diagnose. Herein, we report a case of a 38-year-old pregnant woman at 30 weeks of gestation, with a history of two prior cesarean sections, who presented with severe abdominal pain, vomiting, and constipation, and was eventually diagnosed with both sigmoid volvulus and uterine torsion during surgery. Clinicians should consider the possibility of bowel obstruction when a pregnant woman presents with severe abdominal pain, vomiting, and constipation, as early diagnosis is crucial.

View Article and Find Full Text PDF

William Ladd's procedure for malrotation and volvulus: convincing the world.

J Pediatr Surg

September 2025

Mercer University School of Medicine, Columbus Campus, Columbus GA 31901. Electronic address:

For one considered "the father of pediatric surgery," William Ladd (1880-1967) has few eponymous procedures and terms that bear his name. The Ladd procedure is a series of procedures to address malrotation of the intestine and midgut volvulus. Also bearing his name are Ladd's bands, obstructing adhesions that cross the duodenum as they bind the nonrotated cecum high in the right upper quadrant to the retroperitoneum.

View Article and Find Full Text PDF

Introduction: Situs inversus totalis is an uncommon congenital disease characterized by the full transposition of thoracic and abdominal organs. Sigmoid volvulus, an unusual but potentially catastrophic cause of major bowel obstruction, is rarely associated with Situs inversus.

Case Presentation: A 76-year-old male presented with abdominal pain and obstipation for 5 days.

View Article and Find Full Text PDF

One of the extremely uncommon manifestations of malrotation is nonrotation, a condition that arises due to the complete failure of the midgut to rotate 270 degrees. The true prevalence in adults remains obscure due to the scarcity of the condition. A standard surgical approach to management is therefore lacking, and an increasing number of case reports is required to establish evidence-based recommendations.

View Article and Find Full Text PDF