Enteric duplication cysts in paediatric population along with literature review

Sana Ahuja1, Rashi Maheshwari1, Saba Naaz1

  • 1Department of Pathology, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.

Insights

Enteric duplication cysts present with varied symptoms, often mimicking intestinal obstruction. Early surgical excision is crucial for a good prognosis in pediatric cases.

Area of Science:

  • Pediatric Surgery
  • Gastroenterology
  • Developmental Biology

Background:

  • Enteric duplication cysts are rare congenital anomalies, presenting a diagnostic challenge due to varied clinical manifestations.
  • Symptoms range from nausea and vomiting to severe complications like intestinal obstruction and perforation, depending on cyst location.

Observation:

  • A retrospective review identified four pediatric cases of enteric duplication cysts between 2019 and 2023.
  • Presentations included intestinal obstruction (abdominal distension, pain) in three patients and an antenatally detected mass in one.
  • The cases involved ileal (3) and cecal (1) duplication cysts, with histological findings of ileal/cecal mucosa and one instance of ectopic gastric mucosa.

Findings:

  • Surgical excision is the definitive treatment for enteric duplication cysts.
  • Radiological imaging aids in provisional diagnosis, but histopathological examination confirms the final diagnosis.
  • Early diagnosis and treatment are essential to prevent complications and ensure favorable patient outcomes.

Implications:

  • This case series highlights the importance of considering enteric duplication cysts in the differential diagnosis of pediatric abdominal masses and obstruction.
  • Understanding the varied presentations and confirming diagnosis via histopathology are key for timely surgical intervention.
  • Prompt management of these congenital anomalies leads to improved patient prognosis and reduces long-term morbidity.