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Von Hippel-Lindau disease involving pancreas and biliary system: A rare case report
RATIONALE: Von Hippel-Lindau (VHL) disease is a rare inherited, autosomal-dominant syndrome caused by heterozygous germline mutations in the VHL gene. VHL patients are prone to develop benign and malignant tumors and cysts in multiple organ systems involving kidneys, pancreas and central nervous sys...
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| Publicado no: | Medicine (Baltimore) |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer Health
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5228696/ https://ncbi.nlm.nih.gov/pubmed/28072736 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000005808 |
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