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Autoimmune pancreatitis characterized by predominant CD8+ T lymphocyte infiltration
Autoimmune pancreatitis (AIP) is a rare form of pancreatitis characterized by prominent lymphocyte infiltration and pancreatic fibrosis resulting in organ dysfunction. The pathogenesis and pathology of AIP remain unknown. A 64-year-old Chinese man presented with symptoms and signs of bile duct obstr...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Baishideng Publishing Group Co., Limited
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3225101/ https://ncbi.nlm.nih.gov/pubmed/22147972 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.v17.i41.4635 |
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