A recent retrospective study (K Queliza et al. JPGN 2018; 66: 620-23) describes seven patients with granulomatous disease in the upper GI tract who were diagnosed with ulcerative colitis.
This study examined patients at a single center between 2007-2016 with ages ranging from 2 years to 17 years. Median time of followup is not provided. Two patients required colectomy. All patients had non-casseating granulomas identified in either the stomach or duodenum (or both) along with moderate to severe pancolitis. All of the patients had extensive investigations, generally cross-sectional imaging (MRE or CT) or capsule endoscopy
- “The final classification of IBD was based on expert opinion from gastroenterologists, radiologists, and pathologists upon thorough review of the medical records.”
My take: This study highlights the confusion of the essentially binary classification of IBD into either Crohn’s disease or ulcerative colitis, when in fact there are hundreds of genetic mutations which give rise to inflammatory bowel disease. Given that granulomas are a hallmark of Crohn’s disease and there are no pathognomic features of ulcerative colitis, only time will tell if these patients have an ulcerative colitis phenotype. I wonder how many centers would take exception to this classification and describe these patients as ‘indeterminate’ colitis/IBDU (IBD unclassified).
Related blog posts:
- ESPGHAN IBD Diagnostic Practice … – gutsandgrowth
- Serology in IBD | gutsandgrowth
- Paris Classification of Pediatric Crohn’s Disease | gutsandgrowth
- How helpful are serologies in IBD