نتایج جستجو برای: autoimmune pancreatitis
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Autoimmune pancreatitis (AIP) is a newly described entity with characteristic clinical, radiological, serological, and histological features, in which autoimmune mechanisms seem to be involved in pathogenesis. Many new clinical aspects of AIP have been clarified during 10 years, and AIP has become a distinct entity recognized worldwide. However, precise pathogenesis or pathophysiology remains u...
It is now clear that are two histological types (Type-1 and Type-2) of autoimmune pancreatitis (AIP). The histological pattern of Type-1 AIP, or traditional AIP, is called lymphoplasmacytic sclerosing pancreatitis (LPSP). The histological pattern of Type-2 AIP is characterized by neutrophilic infiltration in the epithelium of the pancreatic duct. In general, Type-2 AIP patients are younger, may...
Autoimmune pancreatitis (AIP) is a newly recognized entity of pancreatitis that can mimic malignancy (6). Patients with AIP and pancreatic cancer have many clinical features in common, such as a higher prevalence among elderly males, frequent presentation with painless jaundice, development of diabetes mellitus, and elevated levels of serum tumor markers. Radiologically, focal swelling of the p...
Autoimmune pancreatitis (AIP) is a rare disorder of presumed autoimmune etiology with specific pathologic features, and is an increasingly recognized clinical condition. AIP is characterized histologically by fibrosis with dense infiltration of T lymphocytes and IgG4positive plasma cells in the peripancreatic and interlobular area of the pancreas (1-4). Patients with AIP usually have serum mark...
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