# Annular Pancreas Presenting with Intermittent Duodenal Obstruction in Early Childhood: A Diagnostic Masquerade

**Authors:** Maria Rogalidou, Georgios Papagiannis, Paraskevi Galina, Evangelia Lykopoulou, Konstantina Dimakou, Alexandra Papadopoulou

PMC · DOI: 10.3390/reports9010026 · Reports - Clinical Practice and Surgical Cases · 2026-01-15

## TL;DR

A rare case of annular pancreas in a young child presented with intermittent vomiting and was diagnosed using imaging and endoscopy, leading to successful surgical treatment.

## Contribution

Highlights the diagnostic challenges of annular pancreas in older children with atypical symptoms and emphasizes the role of multimodal imaging.

## Key findings

- Annular pancreas can present with intermittent vomiting without typical signs like bilious vomiting or failure to thrive.
- Contrast-enhanced CT and endoscopy confirmed annular pancreas in a 2-year and 10-month-old child.
- Surgical bypass provided complete symptom resolution and excellent long-term outcomes.

## Abstract

Background and Clinical Significance: Annular pancreas is a rare congenital anomaly in which pancreatic tissue partially or completely encircles the duodenum, potentially causing duodenal obstruction. Clinical presentation varies from asymptomatic cases to persistent vomiting, feeding intolerance, and failure to thrive, often leading to delayed diagnosis. Case Presentation: We report a 2-year and 10-month-old girl with a long-standing history of intermittent, recurrent vomiting since the neonatal period, without growth impairment or other alarming symptoms. Initial imaging suggested proximal duodenal dilation, with suspicion for superior mesenteric artery (SMA) syndrome. Endoscopy revealed mechanical obstruction at the second portion of the duodenum. Contrast-enhanced CT confirmed annular pancreas partially encircling the duodenum. The patient underwent duodeno-duodenostomy with an uneventful postoperative course and complete resolution of symptoms. This case illustrates the diagnostic challenges of annular pancreas in older children with atypical presentations. Multimodal imaging is crucial for accurate diagnosis. Surgical bypass remains the definitive treatment, offering excellent long-term outcomes. Conclusions: Persistent or recurrent vomiting in children, even without classic signs such as bilious vomiting or failure to thrive, should prompt consideration of annular pancreas. Early recognition and timely surgical intervention can prevent prolonged morbidity and ensure normal growth and development.

## Linked entities

- **Diseases:** annular pancreas (MONDO:0008183), superior mesenteric artery syndrome (MONDO:0002687)

## Full-text entities

- **Diseases:** superior mesenteric artery (SMA) syndrome (MESH:D013478), growth impairment (MESH:D006130), bilious vomiting (MESH:D014839), duodenal dilation (MESH:D004382), failure to thrive (MESH:D005183), congenital anomaly (MESH:D000013), Annular Pancreas (MESH:C536376), Duodenal Obstruction (MESH:D004380)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12821695/full.md

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Source: https://tomesphere.com/paper/PMC12821695