Cargando…
Neurofibromatosis-related phaeochromocytoma: two cases with large tumours and elevated plasma methoxytyramine
We present two cases of adrenal phaeochromocytoma in patients with a previous diagnosis of neurofibromatosis type 1 (NF1). One had an adrenergic phenotype. The other had a more noradrenergic phenotype. Both had large primary tumours, which increases the likelihood of malignancy. Both also had elevat...
Autores principales: | Teasdale, Stephanie, Reda, Elham |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4533181/ https://www.ncbi.nlm.nih.gov/pubmed/26273474 http://dx.doi.org/10.1530/EDM-15-0059 |
Ejemplares similares
-
Phaeochromocytoma presenting with polyuria: an uncommon presentation of a rare tumour
por: Atapattu, N, et al.
Publicado: (2014) -
Phaeochromocytoma and Acromegaly: a unifying diagnosis
por: Mumby, C, et al.
Publicado: (2014) -
Rare presentation of collapse and cardiomyopathy in phaeochromocytoma
por: Singh, Rajiv, et al.
Publicado: (2021) -
Bowel perforation complicating an ACTH-secreting
phaeochromocytoma
por: Flynn, Elise, et al.
Publicado: (2016) -
Adrenal insufficiency in a child following unilateral excision of a dual-hormone secreting phaeochromocytoma
por: Sjoeholm, Annika, et al.
Publicado: (2015)