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Colonic Malakoplakia: A Rare Finding in a Healthy Male
Rawad A Yared1, Hussein A Badran1, Mohammed Hussein Kamareddine2
1Department of Gastroenterology, Saint George Hospital University Medical Center, University of Balamand, Beirut, Lebanon.
Malakoplakia, a rare granulomatous disease, can affect various organs. This case highlights an isolated colonic malakoplakia in the transverse colon, diagnosed via endoscopy and histology.
Area of Science:
- Gastroenterology
- Pathology
- Rare Diseases
Background:
- Malakoplakia is a rare chronic granulomatous disease affecting multiple organs, with the gastrointestinal tract being a common site outside the urinary tract.
- Colonic malakoplakia is infrequently reported and often associated with systemic diseases or colorectal adenocarcinoma.
- Most reported colonic malakoplakia cases involve the rectum, sigmoid, or right colon.
Observation:
- A 65-year-old male presented with abdominal pain and unintentional weight loss.
- Colonoscopy revealed an isolated, large, flat, soft, and pale lesion in the transverse colon.
- Physical examination findings were unremarkable.
Findings:
- Histopathological examination showed lamina propria expansion with inflammatory cells and polygonal cells.
- Von Kossa stain revealed intracytoplasmic granular inclusions.
- Numerous Michaelis-Gutmann bodies were identified, confirming the diagnosis of colonic malakoplakia.
Implications:
- This case represents a rare instance of isolated transverse colonic malakoplakia diagnosed through endoscopic specimens.
- Highlights the importance of considering malakoplakia in the differential diagnosis of colonic lesions, even when isolated.
- Contributes to the understanding of rare gastrointestinal manifestations of malakoplakia.
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