Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation

von Hippel-Lindau (VHL) disease is an autosomal dominantly inherited disorder, characterized by hemangioblastomas of the retina and central nervous system (CNS); renal cysts; clear cell carcinoma; pheochromocytoma (PCC); endolymphatic sac tumors; cystadenomas of the epididymis in males; broad ligame...

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Detalles Bibliográficos
Autores principales: Dağdeviren Çakır, Aydilek, Turan, Hande, Aykut, Ayça, Durmaz, Asude, Ercan, Oya, Evliyaoğlu, Olcay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985389/
https://www.ncbi.nlm.nih.gov/pubmed/29022557
http://dx.doi.org/10.4274/jcrpe.5078

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985389/
https://www.ncbi.nlm.nih.gov/pubmed/29022557
http://dx.doi.org/10.4274/jcrpe.5078

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