A Case of Von Hippel–Lindau Disease with Bilateral Pheochromocytoma and Ectopic Hypersecretion of Intact Parathyroid Hormone in an Adolescent Girl

Von Hippel–Lindau disease is an autosomal dominant inherited syndrome predisposing to a variety of highly vascularised tumors in different organs. Although bilateral pheochromocytoma was reported in patients with von Hippel–Lindau disease, the coexistence of primary hyperparathyroidism is not a comm...

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Detalles Bibliográficos
Autores principales: Belaid, Rym, Oueslati, Ibtissem, Chihaoui, Melika, Yazidi, Meriem, Grira, Wafa, Chaker, Fatma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7428957/
https://www.ncbi.nlm.nih.gov/pubmed/32832168
http://dx.doi.org/10.1155/2020/8824640

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7428957/
https://www.ncbi.nlm.nih.gov/pubmed/32832168
http://dx.doi.org/10.1155/2020/8824640

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