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Korean Journal of Medicine ; : 466-471, 2014.
Artigo em Coreano | WPRIM | ID: wpr-192836

RESUMO

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.


Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Doenças Autoimunes , Fibrose , Coreia (Geográfico) , Mucinas , Neoplasias Pancreáticas , Pancreatite , Pancreatite Crônica
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