autoimmune pancreatitis/fatigue

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Autoimmune Pancreatitis in an Adolescent: A Diagnostic Challenge

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Autoimmune pancreatitis (AIP) is a distinct subtype of pancreatitis, rare in the pediatric population. Its pathophysiology is poorly understood. A pancreatic focal mass is frequently the clinical presentation, which imposes the differential diagnosis with a pancreatic tumor. This distinction is

[The clinical characteristics of 32 patients with autoimmune pancreatitis].

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OBJECTIVE To explore the clinical characteristics and diagnosis of autoimmune pancreatitis (AIP) with the aim to raise awareness of AIP. METHODS Clinical data of 32 patients with AIP were retrospectively analyzed, including clinical manifestations, imaging features, laboratory examination,

IgG4 Sclerosing Cholangitis - an Inflammation Imitating Tumour of the Pancreas and Biliary Tract.

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Immunoglobulin (Ig) G4 associated sclerosing cholangitis is a rare inflammatory disease of the biliary tract. Although it is a very progressive condition, it responds to steroid therapy. IgG4 associated sclerosing cholangitis can mimic pancreatic carcinoma, cholangiocarcinoma, and

Recurrent steroid-responsive pancreatitis associated with myelodysplastic syndrome and transformations.

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Several paraneoplastic inflammatory conditions, particularly autoimmune diseases, have been described in association with myelodysplastic syndromes (MDS). However, to date, recurrent acute pancreatitis has never been described in association with MDS. A 44-year-old man presented with prolonged fever

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