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Brown Bowel Syndrome: A Multi-institutional Case Series
Christina A Arnold1, Allen P Burke2, Edward Calomeni3
1Department of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO.
Brown bowel syndrome (BBS) is a rare condition characterized by vitamin E deficiency and lipofuscin deposition. Diagnosis involves identifying lipofuscin pigment in smooth muscle cells, crucial for distinguishing it from malignancy.
Area of Science:
- Gastroenterology
- Pathology
- Nutritional Science
Background:
- Brown bowel syndrome (BBS) is a rare condition.
- It is characterized by lipofuscin deposition in the muscularis propria.
- BBS is associated with vitamin E deficiency and malnutrition.
Purpose of the Study:
- To describe the clinical, imaging, and histopathologic features of Brown Bowel Syndrome.
- To highlight the diagnostic criteria and clinical significance of BBS.
- To differentiate BBS from other gastrointestinal conditions, including malignancy.
Main Methods:
- Retrospective review of eight unique cases of BBS.
- Analysis of clinical presentation, comorbidities, imaging studies, and surgical/autopsy specimens.
- Histopathologic examination including special stains and electron microscopy to identify lipofuscin pigment.
Main Results:
- Eight patients (5 men, 3 women; mean age 58.6 years) with BBS were identified.
- Common comorbidities included bariatric surgery, malnutrition, Crohn's disease, and prior bowel resections.
- Histology revealed characteristic brown, granular cytoplasmic pigment (lipofuscin) in smooth muscle cells, predominantly in the small bowel muscularis propria.
Conclusions:
- Brown bowel syndrome is a distinct entity linked to vitamin E deficiency.
- Histopathologic identification of lipofuscin in the muscularis propria is key for diagnosis.
- Recognizing BBS is important due to its association with malnutrition and potential to mimic malignancy.
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