Question: A 60-year-old Armenian-born female living in Australia presented with a 2-month history of progressive watery diarrhea and weight loss and was diagnosed with intestinal failure secondary to malabsorption. Her medical history was notable for Familial Mediterranean Fever (FMF) diagnosed in childhood and genetically confirmed with two MEFV pathogenic variants. Her FMF had been intermittently active but had been clinically stable for more than 20 years on colchicine 0.5 mg twice daily regularly, albeit with occasional flares of serositis.
We will be happy to hear your thoughts