Cargando…
Bilateral Pheochromocytoma and Paraganglioma Tumors Due to Von Hippel-Lindau Syndrome in a 15-Year-Old Boy: A Case Report
Pheochromocytomas and paragangliomas are catecholamine-secreting tumors that originate from chromaffin cells of the adrenal medulla and autonomic neural ganglia, respectively. Patients with pheochromocytomas and paragangliomas typically present with paroxysmal headache, sweating, tachycardia, and hy...
Autores principales: | Khalaf, Saeed, Jamal, Hasan F, Alawi, Zahra S, Alsaeed, Mahmood |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676564/ https://www.ncbi.nlm.nih.gov/pubmed/38021838 http://dx.doi.org/10.7759/cureus.47787 |
Ejemplares similares
-
Ocular Manifestations of von Hippel-Lindau Disease
por: Ruppert, Misty D, et al.
Publicado: (2019) -
Pheochromocytomas and paragangliomas in von Hippel–Lindau disease: not a needle in a haystack
por: Castro-Teles, João, et al.
Publicado: (2021) -
Bilateral papillopathy as a presenting sign of pheochromocytoma associated with von Hippel–Lindau disease
por: Shah, Veeral, et al.
Publicado: (2014) -
Bilateral Pheochromocytomas in a Patient with Y175C Von Hippel-Lindau Mutation
por: Astapova, Olga, et al.
Publicado: (2018) -
Bilateral Pheochromocytoma Due to Von Hippel Lindau With Adrenal-Sparing Adrenalectomy in a Child
por: Hilk, Kelly, et al.
Publicado: (2021)