Tidak Ya
Medikamentosa AVS
Bilateral--> Medikamentosa
Pemayun, Tjokorda GD., Ridho N., Maretina W.W., Ardy S. Primary Hyperaldosteronism Due
to Adrenocortical Adenoma: a Case Report. Acta Med Indones - Indones J Intern Med. 2017. 49 (3).
249-254.
Rossi, GP. AN UPDATE OF THE GUIDELINES FOR DIAGNOSIS AND MANAGEMENT OF PRIMARY
ALDOSTERONISM. European Society of Hypertension : Scientific Newsletter Update on Hypertension
Management. 26 (79).
Vilela, L.A.P., Madson Q.A. Diagnosis and management of primary aldosteronism. Arch
Endocrinol Metab. 2017;61/3. 305-312.
Sossa, J., Dedjinnin J.G.A., Dodji M.IY.
7. Diagnosis Banding
Similar presentations have been observed in essential hypertension, Liddle syndrome,
syndrome of apparent mineralocorticoid excess, congenital adrenal hyperplasia, primary
glucocorticoid resistance, and ectopic adrenocorticotropic hormone (ACTH) syndrome.Essential
hypertension presents with a normal PAC/PRA ratio. Liddle syndrome will have low aldosterone
levels and will typically present in childhood. Syndrome of apparent mineralocorticoid excess
will present with low aldosterone levels, high urinary free cortisol levels, hereditary
implications, and/or a history of excessive licorice consumption. Congenital adrenal hyperplasia
will have a family history of 11-beta-hydroxylase or 17-alpha-hydroxylase deficiency and low
aldosterone levels. Primary glucocorticoid resistance will have low aldosterone levels, an
elevated ACTH and cortisol, and a family history of this syndrome. Ectopic ACTH syndrome will
have elevated ACTH that cannot be suppressed with high-dose dexamethasone, and these
patients will have an underlying tumor. Dominguez
Byrd, JB., Adina FT., Richard JA. Primary Aldosteronism Practical Approach to Diagnosis and
Management. Circulation. 2018;138:823–835. DOI: 10.1161/CIRCULATIONAHA.118.033597