Abstract
Collagenous colitis (CC) is an inflammatory bowel condition of unknown etiology. Systemic sclerosis (SSc) has been associated with CC in a few cases, but it is not clear whether CC could be considered an unusual manifestation of SSc or an independent condition. Here we present a case of SSc-associated CC and compare routine histology and immunofluorescence studies for allograft inflammatory factor 1 and caveolin 1 expression with other cases of CC and healthy controls. All CC biopsies showed characteristic sublaminal collagen accumulation and a decrease of caveolin 1 expression, this latter finding consistent with and common in any fibrotic reaction. In contrast, the expression of allograft inflammatory factor 1 was increased only in the SSc-CC specimen, suggesting a distinct pathogenesis. A literature review revealed 6 previously reported cases of SSc-CC with common clinical features. These observations suggest that CC should be suspected as a rare gastrointestinal complication of SSc and that clinicians should be aware of the possibility in SSc patients developing watery diarrhea.
Original language | English |
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Pages (from-to) | 278-82 |
Number of pages | 5 |
Journal | Journal of Clinical Rheumatology |
Volume | 20 |
Issue number | 5 |
DOIs | |
Publication status | Published - Aug 2014 |
Keywords
- Aged
- Biopsy, Needle
- Budesonide/administration & dosage
- Colitis, Collagenous/complications
- Colonoscopy/methods
- Drug Administration Schedule
- Female
- Follow-Up Studies
- Humans
- Immunohistochemistry
- Lansoprazole/administration & dosage
- Risk Assessment
- Scleroderma, Systemic/complications
- Severity of Illness Index
- Tomography, X-Ray Computed/methods
- Treatment Outcome