Objective: To report an uncommon presentation of a rare case of autoimmune polyglandular syndrome type IIIb in a patient presenting as well with Small Duct Primary Sclerosing Cholangitis. Clinical Presentation and Intervention: A 42-year-old man presented with jaundice and intermittent fever. Blood tests showed macrocytic anaemia due to vitamin B 12 deficiency compatible with Biermer’s disease. A thyroid function test was consistent with hyperthyroidism compatible with Basedow’s disease. And Liver biopsy revealed signs compatible with Small Duct Sclerosing Cholangitis. A final diagnosis of Small Duct Sclerosing Cholangitis with Biermer’s disease and Basedow’s disease, which constituted autoimmune polyglandular syndrome type IIIb, was made and the patient was treated with L-thyroxine, vitamin B 12 injection and Ursodeoxycholic acid with a impressive improvement during his follow up. Conclusion: This case showed a rare combination between APS type IIIb and Small Duct Sclerosing Cholangitis and that the presence of one autoimmune endocrine disease should prompt clinicians to look for other coexisting autoimmune diseases which may be asymptomatic.

Retrograde endoscopic cholangiopancreatography (ERCP) retains a prominent place in the therapeutic management of bilio-pancreatic pathologies, in particular lithiasis disease. Its complications are now well known and are dominated by acute pancreatitis. The aim of our work is to assess the frequency and predictors of complications of ERCP.We retrospectively included all consecutive patients who received an ERCP, between January 2018 and April 2019 in the gastroenterology I Department of the Military Instruction Hospital Mohamed V in Rabat, for a lithiasis pathology. Clinical, biological and endoscopic data were collected from patient records.Statistical analysis was performed by Spss20 software using the binary logistic regression model in univariate and multivariate analyzes. The associated factors studied are: age, sex, history of ERCP, taking NSAIDs before the gesture, catheterization of the pancreatic duct and the number of passages in the Wirsung, the achievement of a pre-cut and the total duration of the procedure.

Severe acute colitis is a medical and surgical emergency that involves the short-term life threatening. The diagnosis of CAG is based on the combination of clinical and biological criteria and can be supported by morphological criteria (endoscopy, scanner). It complicates ulcerative colitis (UC) as well as Crohn's disease.It is a serious complication which, in the absence of proper care, in a specialized environment, is likely to jeopardize the vital prognosis. Intravenous corticosteroid therapy (CO IV) is the first-line medical treatment for AGC.The objective of our work is to assess the predictive factors of the response to intravenous corticosteroid therapy during severe acute colitis. This is an observational study spread over 2 years, covering 27 cases of severe acute colitis collected within our department. The Severe acute colitis was defined by a Lichtiger score greater than 10. Clinical, biological, endoscopic and radiological data were collected and analyzed by SPSS20 software.