Epidemiology,clinical presentation,diagnosis and treatment of autoimmune pancreatitis: A retrospective analysis of 53 patients |
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Affiliation: | 1. Department of Medicine A, University Medicine Greifswald, Ernst-Moritz-Arndt-University Greifswald, Germany;2. Lister Department of Surgery, Glasgow Royal Infirmary, Glasgow, United Kingdom;3. Department of Pathology, Southern General Hospital, Glasgow, United Kingdom;2. Department of Clinical Laboratory, Anhui Medical University Affiliated Provincial Hospital, Hefei, Anhui, China;1. Department of Gastroenterology, Changhai Hospital, Second Military Medical University, Shanghai 200433, China;2. Department of Pathology, Changhai Hospital, Second Military Medical University, Shanghai 200433, China;3. Department of Nuclear Medicine, Changhai Hospital, Second Military Medical University, Shanghai 200433, China;4. Department of Radiology, Changhai Hospital, Second Military Medical University, Shanghai 200433, China;5. Department of General Surgery, Changhai Hospital, Second Military Medical University, Shanghai 200433, China;6. Department of Surgical Oncology, Chinese PLA General Hospital, Beijing 100853, China;7. Department of General Surgery, Huashan Hospital, Fudan University, Shanghai 200040, China |
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Abstract: | BackgroundMost of the data about epidemiology, clinical presentation and treatment of autoimmune pancreatitis (AIP) is based on case series or small study groups. We therefore analyzed all cases of AIP treated at our clinic retrospectively.MethodsWe searched our clinical database for the diagnosis pancreatitis between January 2007 and June 2014, selected patients with AIP and entered all relevant information in a database for statistical analysis.ResultsIn total 53 patients with AIP were treated at our institution, 62% with type 1 and 23% with type 2 AIP. Gender distribution was male/female 3.1:1 for type 1 and 1:1.2 for type 2 AIP. The median age was 63.0 and 32.5 years for type 1 and type 2 AIP, respectively. The most common symptom is abdominal pain particular in patients with type 2 AIP whereas jaundice was only apparent in patients with type 1 AIP. The international diagnostic criteria seem to facilitate diagnosis of AIP as unnecessary pancreatic surgery in patients with AIP decreases. In 62.6% of the patients therapy was indicated and 84.8% showed a response to initial therapy with steroids. Recurring disease occurred in 28.3% of the cases but only 3.8% suffered a second relapse. Permanent maintenance therapy with steroids or additional therapy with immunomodulatory drugs is successful in recurring disease.ConclusionOur data further corroborate previous findings on epidemiology, clinical presentation and treatment of AIP. AIP is a well manageable autoimmune disease in most patients. Better biopsy techniques and simplified diagnostic criteria might further alleviate diagnosis of AIP. |
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Keywords: | Autoimmune pancreatitis Chronic pancreatitis Idiopathic duct centric pancreatitis IgG4 Lymphoplasmacytic sclerosing pancreatitis IgG4-related disease |
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