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Malakoplakia: A rare cause of hematochezia in pediatric patients
Ariel Porto1, Jonathan Lebowitz1, Robert Byrd2
1Division of Gastroenterology, Hepatology, & Nutrition, Ann & Robert H. Lurie Children's Hospital of Chicago Northwestern University Feinberg School of Medicine Chicago Illinois USA.
Abstract:
Malakoplakia is a rare inflammatory condition characterized by impaired macrophages unable to completely digest and kill phagocytized bacteria, resulting in partially digested bacterial components accumulating within the phagolysosome. Malakoplakia typically presents in immunocompromised individuals due to underlying disease or to medication effects and is rarely diagnosed in the pediatric population. The urinary tract is the most commonly involved site, followed by the gastrointestinal (GI) tract, mainly affecting the descending colon, sigmoid colon, and rectum. Treatment focuses on the use of antibiotics that concentrate in macrophages such as quinolones and trimethoprim-sulfamethoxazole as well as cholinergic agents such as bethanechol, which raise intracellular levels of cyclic guanosine monophosphate in macrophages to improve bactericidal activity. We report a rare case of GI tract malakoplakia in a pediatric patient undergoing treatment for leukemia.
Insights
Malakoplakia, a rare inflammatory condition, involves impaired macrophages. This case highlights gastrointestinal malakoplakia in a pediatric leukemia patient, emphasizing its rarity in children.
Area of Science:
- Medical Pathology
- Immunology
- Pediatric Gastroenterology
Background:
- Malakoplakia is a rare inflammatory disorder characterized by defective macrophage phagolysosomal activity.
- It typically affects immunocompromised individuals and is uncommon in pediatric populations.
- The urinary tract is the most frequent site, followed by the gastrointestinal tract.
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