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International consensus guidelines 2012 for the management of IPMN and MCN of the pancreas.
TLDR
The present guidelines include recent information and recommendations based on the current understanding, and highlight issues that remain controversial and areas where further research is required. Expand
International Consensus Guidelines for Management of Intraductal Papillary Mucinous Neoplasms and Mucinous Cystic Neoplasms of the Pancreas
TLDR
Ovarian-type stroma has been proposed as a requisite to distinguish MCN from IPMN, and some other distinct features to characterize IPMN and MCN have been identified, but there remain ambiguities between the two diseases. Expand
Consensus statement on the pathology of IgG4-related disease
TLDR
This statement proposes a terminology scheme for the diagnosis of IgG4-related disease that is based primarily on the morphological appearance on biopsy, and advocates the use of strict criteria for accepting newly proposed entities or sites as components of the IgG 4- related disease spectrum. Expand
International Consensus Diagnostic Criteria for Autoimmune Pancreatitis: Guidelines of the International Association of Pancreatology
TLDR
The categorization of AIP into types 1 and 2 should be helpful for further clarification of the clinical features, pathogenesis, and natural history of these diseases. Expand
Immunoglobulin G4-associated cholangitis: clinical profile and response to therapy.
TLDR
IAC should be suspected in unexplained biliary strictures associated with increased serum IgG4 and unexplained pancreatic disease, especially with proximal strictures, and the role of immunomodulatory drugs for relapses needs further study. Expand
Diagnosis of autoimmune pancreatitis: the Mayo Clinic experience.
TLDR
D diagnosis of autoimmune pancreatitis can be made in patients with > or =1 of these criteria: diagnostic histology, characteristic imaging on computed tomography and pancreatography with elevated serum IgG4 level, or response to steroid therapy of pancreatic/extrapancreatic manifestations of AIP. Expand
Idiopathic Chronic Pancreatitis With Periductal Lymphoplasmacytic Infiltration: Clinicopathologic Features of 35 Cases
TLDR
It is concluded that idiopathic chronic pancreatitis with lymphoplasmacytic infiltration, sometimes called autoimmune pancreatitis, consists of at least two different processes and one of these is a histologically unique lesion and could be a pancreatic manifestation of idiopATHic fibrosclerosing disorders. Expand
International Consensus Guidance Statement on the Management and Treatment of IgG4‐Related Disease
TLDR
A. H. Wallace, J. L. Carruthers, S. L€ ohr, Y. Khosroshahi, Z. Chari, E. Della-Torre, L. Frulloni, H. Expand
Diagnosis of IgG4-related tubulointerstitial nephritis.
TLDR
Because no single test definitively diagnoses IgG4-related systemic disease, a combination of histologic, immunophenotypic, clinical, radiographic, and laboratory features are relied on to support diagnostic criteria that can distinguish IgG 4-TIN from other types of TIN. Expand
Study of recurrence after surgical resection of intraductal papillary mucinous neoplasm of the pancreas.
TLDR
Invasive intraductal papillary mucinous neoplasm recurs frequently even after a complete "curative" resection and portends poor survival, and survival is excellent regardless of the degree of epithelial dysplasia in the tumor. Expand
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