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Cecal Duplication Cyst Presenting With Hematochezia

Serina Beydoun1,2, James W Davis2,3, Namir Al-Ansari1,2

  • 1Department of Pediatric Gastroenterology, Children's Hospital of Michigan, Detroit, MI.

ACG Case Reports Journal
|March 6, 2025
PubMed

Insights

Enteric duplication cysts are rare congenital anomalies. This case highlights a cecal duplication cyst presenting as hematochezia in an infant, emphasizing the need for timely diagnosis and surgical intervention to prevent serious complications.

Area of Science:

  • Pediatric Surgery
  • Gastroenterology
  • Congenital Anomalies

Background:

  • Enteric duplication cysts are uncommon congenital malformations.
  • They can manifest with vague symptoms, complicating early diagnosis.
  • Prompt identification is crucial for preventing severe outcomes.

Observation:

  • A 13-month-old female presented with hematochezia, initially misdiagnosed as viral gastroenteritis.
  • Imaging studies revealed a cecal duplication cyst.
  • The patient underwent surgical resection via ileocecectomy.

Findings:

  • Pathological examination confirmed the diagnosis of a cecal duplication cyst.
  • The surgical intervention successfully addressed the anomaly.
  • This case underscores the diagnostic challenges associated with enteric duplication cysts.

Implications:

  • Early diagnosis and a multidisciplinary approach are vital for managing enteric duplication cysts.
  • Surgical management is essential to avoid complications like bowel obstruction and perforation.
  • Optimal patient outcomes depend on prompt and accurate diagnosis and treatment.

Keywords:
duplication cysthematocheziapediatric

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