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Korean Journal of Medicine ; : 466-471, 2014.
Article in Korean | WPRIM | ID: wpr-192836

ABSTRACT

Autoimmune pancreatitis (AIP) has been increasingly recognized in recent years, and most cases are diagnosed without surgery. However, focal-type mass-forming AIP is difficult to differentiate from pancreatic cancer without surgical resection. A 61-year-old male patient with a clinical impression of pancreatic cancer underwent surgery. A postoperative pathologic examination showed locally dense lymphoplasma cell infiltration and numerous lymphoid follicles with fibrosis and a low-grade intraductal papillary mucinous neoplasm (IPMN). Here, we report the first case of localized mass-forming AIP combined with a low-grade IPMN, which mimicked pancreatic cancer, in Korea.


Subject(s)
Humans , Male , Middle Aged , Autoimmune Diseases , Fibrosis , Korea , Mucins , Pancreatic Neoplasms , Pancreatitis , Pancreatitis, Chronic
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