Enterocolitis-Associated Pseudo-Obstruction in a Sickle Cell Patient: A Rare Abdominal Catastrophe
Munir Ahmad, Mohammed Alblooshi, Abdalla Aboelkheir, Masih Abdul Kader

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.
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…
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Taxonomy
TopicsHemoglobinopathies and Related Disorders · Iron Metabolism and Disorders · Prenatal Screening and Diagnostics
