Cargando…
Bowel perforation complicating an ACTH-secreting phaeochromocytoma
ACTH-secreting phaeochromocytoma (ASP) is a rare cause of ACTH-dependent Cushing’s syndrome (CS). We report the case of a 63-year-old female presenting with CS secondary to an ASP complicated by bowel perforation. This case report highlights ASP as an uncommon but important cause of ectopic ACTH sec...
Autores principales: | Flynn, Elise, Baqar, Sara, Liu, Dorothy, Ekinci, Elif I, Farrell, Stephen, Zajac, Jeffrey D, De Luise, Mario, Seeman, Ego |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5291089/ https://www.ncbi.nlm.nih.gov/pubmed/28203371 http://dx.doi.org/10.1530/EDM-16-0061 |
Ejemplares similares
-
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) -
Adrenal insufficiency in a child following unilateral excision of a dual-hormone secreting phaeochromocytoma
por: Sjoeholm, Annika, et al.
Publicado: (2015) -
Phaeochromocytoma presenting with polyuria: an uncommon presentation of a rare tumour
por: Atapattu, N, et al.
Publicado: (2014) -
Neurofibromatosis-related phaeochromocytoma: two cases with large tumours and elevated plasma methoxytyramine
por: Teasdale, Stephanie, et al.
Publicado: (2015)