Cargando…
A rare presentation of an ACTH‐producing high‐grade large cell neuroendocrine carcinoma with Cushing’s syndrome
High‐grade neuroendocrine tumors (HGNET) are rare neoplasms composed of neural and hormonal with only around 42 cases reported in the last 20 years1. Herein, we describe a rare case of pancreatic HGNET, large cell type, associated with a Cushing's syndrome presentation.
Autores principales: | Essien, Francis, Persaud, Christine, Dado, David, Eden, Rina, Tate, Joshua, Shahin, George |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8666948/ https://www.ncbi.nlm.nih.gov/pubmed/34938550 http://dx.doi.org/10.1002/ccr3.5168 |
Ejemplares similares
-
ACTH-Producing Neuroendocrine Carcinoma of the Liver with Cushing's Syndrome
por: Sandozi, Mudassar, et al.
Publicado: (2023) -
The Diagnosis and Management of a Rare ACTH-Producing Neuroendocrine Tumor Causing Cushing’s Syndrome
por: Findlay, Ryan, et al.
Publicado: (2021) -
ACTH-Producing Thymic Carcinoid: A Rare Cause of Cushing’s Syndrome
por: Rodriguez, Lisette Patricia, et al.
Publicado: (2021) -
Rapidly progressive ACTH-dependent Cushing’s disease masquerading as ectopic ACTH-producing Cushing’s syndrome: illustrative case
por: Yu, Siyuan, et al.
Publicado: (2021) -
SAT-248 Cushing’s Disease with Two ACTH-Producing Pituitary Tumors
por: Mathai, Christine, et al.
Publicado: (2020)