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Presentations of Waugh's syndrome:intra-luminal cecal cyst and trans-anal prolapsing intussusception: a case report
Mansoor Ahmed1, Murad Habib2, Huma Memon3
1Department of Paediatric Surgery, The Children's Hospital, Pakistan Institute of Medical Sciences, Islamabad/Shaheed Zulfiqar Ali Bhutto Medical University, Islamabad, 44000, Pakistan. mansoorahmed1993@live.com.
Insights
Waugh's syndrome, a rare condition combining intussusception and intestinal malrotation, is a pediatric surgical emergency. Early surgical exploration is crucial for managing this congenital anomaly.
Area of Science:
- Pediatric Surgery
- Congenital Anomalies
Background:
- Waugh's syndrome is a rare congenital anomaly defined as intussusception with intestinal malrotation.
- It has an incidence of less than 1% with few reported cases.
Observation:
- Two cases of Waugh's syndrome are presented: an 11-month-old male and a 4-month-old female.
- Both presented with abdominal pain and bleeding per rectum, with sonography showing intussusception and a target sign.
Findings:
- Perioperative findings confirmed intestinal malrotation alongside intussusception, establishing the diagnosis of Waugh's syndrome.
- Surgical intervention included right hemicolectomy and Ladd's procedure.
Implications:
- Waugh syndrome, though rare, presents as a pediatric surgical emergency requiring prompt recognition.
- Management involves patient optimization followed by surgical exploration to address the congenital anomaly.
Background:
Intussusception with intestinal malrotation is termed as Waugh's syndrome. The incidence of Waugh's syndrome is less than 1%. There are very few reported cases. Once presented, it is a pediatric surgical emergency.
Case Presentation:
We present here two cases of Waugh's syndrome: an 11-month-old male patient of Punjabi descent and a 4-month-old female patient of Afghan descent who presented to us with abdominal pain and bleeding per rectum. Abdominal sonography revealed an intussusception with a target sign. They were explored and perioperatively had intestinal malrotation alongside intussusception, thus a diagnosis of Waugh's syndrome was made. A right hemicolectomy and Ladd's procedure was performed.
Conclusion:
Waugh syndrome is a rare congenital anomaly but can present with vague abdominal symptoms. Once presented, it is a pediatric surgical emergency. The patient should be optimized followed by surgical exploration.
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