# Enterocolitis-Associated Pseudo-Obstruction in a Sickle Cell Patient: A Rare Abdominal Catastrophe

**Authors:** Munir Ahmad, Mohammed Alblooshi, Abdalla Aboelkheir, Masih Abdul Kader

PMC · DOI: 10.7759/cureus.81886 · 2025-04-08

## TL;DR

A 14-year-old sickle cell patient experienced severe abdominal issues due to a rare condition involving colonic pseudo-obstruction and enterocolitis, successfully managed without surgery.

## Contribution

Highlights a rare case of enterocolitis-associated pseudo-obstruction in a sickle cell patient, emphasizing multidisciplinary management and infection screening.

## Key findings

- Acute colonic pseudo-obstruction was confirmed in a sickle cell patient with enterocolitis.
- Nonoperative management with decompression, antibiotics, and prokinetics led to improvement.
- Multidisciplinary evaluation avoided unnecessary surgery and improved outcomes.

## Abstract

Acute colonic pseudo-obstruction, also known as Ogilvie’s syndrome, is a rare but critical cause of abdominal pain and distension, potentially mimicking mechanical obstruction or toxic megacolon. Patients with sickle cell disease (SCD) have additional risk factors such as vaso-occlusive crises, chronic hemolysis, and susceptibility to infections, which further complicate diagnosis. We report the case of a 14-year-old male patient with SCD who presented with severe generalized abdominal pain, vomiting, and progressive distension with no fever. Imaging revealed significant colonic dilation and pneumatosis, suggesting pseudo-obstruction or ischemic bowel. Infectious evaluations ultimately identified enteropathogenic Escherichia coli. Despite initial concern for toxic megacolon, a multidisciplinary evaluation by hematology, gastroenterology, infectious disease, and surgery confirmed acute colonic pseudo-obstruction associated with enterocolitis. The patient’s condition was managed nonoperatively with nasogastric decompression, intravenous antibiotics, total parenteral nutrition, and prokinetic agents. Serial imaging demonstrated gradual improvement in colonic distension, facilitating a safe return to oral feeding and subsequent discharge. This case underscores the importance of early recognition of enterocolitis-associated colonic pseudo-obstruction in patients with SCD, highlighting the value of comprehensive infection screening and a careful, multidisciplinary management approach to avoid unnecessary surgery and improve outcomes.

## Linked entities

- **Diseases:** sickle cell disease (MONDO:0011382), Ogilvie’s syndrome (MONDO:0002801), enterocolitis (MONDO:0009172)

## Full-text entities

- **Diseases:** Ogilvie's syndrome (MESH:D003112), fever (MESH:D005334), SCD (MESH:D000755), colonic dilation (MESH:D003108), abdominal pain (MESH:D015746), pneumatosis (MESH:D011006), infection (MESH:D007239), Infectious (MESH:D003141), ischemic bowel (MESH:D012778), Abdominal Catastrophe (MESH:D000007), toxic megacolon (MESH:D008532), vomiting (MESH:D014839), Enterocolitis (MESH:D004760), chronic hemolysis (MESH:D006461), vaso-occlusive crises (MESH:D013224)
- **Chemicals:** prokinetic agents (-)
- **Species:** Escherichia coli (E. coli, species) [taxon 562], Homo sapiens (human, species) [taxon 9606]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11977519/full.md

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Source: https://tomesphere.com/paper/PMC11977519