Cargando…
A case of Williams syndrome with suspected coexisting ectopic aldosterone-producing tumor in the liver
SUMMARY: A 31-year-old man with Williams syndrome (WS) was referred to our hospital because of a 9-year history of hypertension, hypokalemia, and high plasma aldosterone concentration to renin activity ratio. A diagnosis of primary aldosteronism (PA) was clinically confirmed but an abdominal CT scan...
Autores principales: | Baba, Shuhei, Miyoshi, Arina, Obara, Shinji, Usubuchi, Hiroaki, Terae, Satoshi, Sunahara, Masao, Oshima, Takahiro, Misawa, Kazuhito, Tsuji, Takahiro, Takahashi, Bunya, Yamazaki, Yuto, Sasano, Hironobu, Wada, Norio |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576637/ https://www.ncbi.nlm.nih.gov/pubmed/33434178 http://dx.doi.org/10.1530/EDM-20-0057 |
Ejemplares similares
-
SAT-073 A Case of Williams Syndrome Associated with Aldosterone Producing Adrenal Adenoma Mimicking Hepatic Adrenal Rest Tumor
por: Wada, Norio, et al.
Publicado: (2019) -
Metastatic malignant struma ovarii with coexistence of Hashimoto’s thyroiditis
por: Russo, Marco, et al.
Publicado: (2016) -
Familial dysalbuminemic hyperthyroxinemia confounding management of coexistent autoimmune thyroid disease
por: Khoo, Serena, et al.
Publicado: (2020) -
Deterioration of pituitary function without relapse after steroid therapy for IgG4-related hypophysitis
por: Nishi, Nobuyuki, et al.
Publicado: (2021) -
Late bone metastasis from an apparently benign oncocytic follicular thyroid tumor
por: Boronat, Mauro, et al.
Publicado: (2013)