Unilateral adrenal hyperplasia: a rare cause of primary aldosteronism
A 73-year-old gentleman with a background history of long-standing hypertension and hyperlipidaemia presented with one-year history of persistent asymptomatic hypokalaemia associated with metabolic alkalosis. Within a few months, the hypertension worsened, needing increasing...
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my.iium.irep.910792021-07-27T09:10:21Z http://irep.iium.edu.my/91079/ Unilateral adrenal hyperplasia: a rare cause of primary aldosteronism Mahno, Noor Ezmas Muhammad, Rohaizak Abdul Shukur, Nordashima Yaacob, Yazmin RD Surgery A 73-year-old gentleman with a background history of long-standing hypertension and hyperlipidaemia presented with one-year history of persistent asymptomatic hypokalaemia associated with metabolic alkalosis. Within a few months, the hypertension worsened, needing increasing dose of anti-hypertensive agents. Biochemical test showed an elevated aldosterone-renin ratio but the computerized tomography (CT) scan of adrenal did not show any adrenal mass. Arterial stimulation venous sampling (ASVS) lateralized the lesion to the left side. A left retroperitoneal adrenalectomy was performed with immediate reversal of hypokalaemia and improvement of blood pressure control to only single anti-hypertensive agent. IIUM Press 2021-04 Article PeerReviewed application/pdf en http://irep.iium.edu.my/91079/3/91079_Unilateral%20adrenal%20hyperplasia%20a%20rare%20cause%20of%20primary%20aldosteronism_SCOPUS.pdf application/pdf en http://irep.iium.edu.my/91079/4/91079_Unilateral%20adrenal%20hyperplasia%20a%20rare%20cause%20of%20primary%20aldosteronism.pdf Mahno, Noor Ezmas and Muhammad, Rohaizak and Abdul Shukur, Nordashima and Yaacob, Yazmin (2021) Unilateral adrenal hyperplasia: a rare cause of primary aldosteronism. International Medical Journal of Malaysia, 20 (2). pp. 177-180. ISSN 1823-4631 E-ISSN 2735-2285 https://journals.iium.edu.my/kom/index.php/imjm/article/download/1449/1145/7618 https://doi.org/10.31436/imjm.v20i2.1449 |
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RD Surgery Mahno, Noor Ezmas Muhammad, Rohaizak Abdul Shukur, Nordashima Yaacob, Yazmin Unilateral adrenal hyperplasia: a rare cause of primary aldosteronism |
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A 73-year-old gentleman with a background history of long-standing hypertension and hyperlipidaemia presented with one-year history of persistent asymptomatic hypokalaemia associated with metabolic alkalosis. Within a few months, the hypertension worsened, needing increasing dose of anti-hypertensive agents. Biochemical test showed an elevated aldosterone-renin ratio but the computerized tomography (CT) scan of adrenal did not show any adrenal mass. Arterial stimulation venous sampling (ASVS) lateralized the lesion to the left side. A left retroperitoneal adrenalectomy was performed with immediate reversal of hypokalaemia and improvement of blood pressure control to only single anti-hypertensive agent. |
format |
Article |
author |
Mahno, Noor Ezmas Muhammad, Rohaizak Abdul Shukur, Nordashima Yaacob, Yazmin |
author_facet |
Mahno, Noor Ezmas Muhammad, Rohaizak Abdul Shukur, Nordashima Yaacob, Yazmin |
author_sort |
Mahno, Noor Ezmas |
title |
Unilateral adrenal hyperplasia: a rare cause of primary aldosteronism |
title_short |
Unilateral adrenal hyperplasia: a rare cause of primary aldosteronism |
title_full |
Unilateral adrenal hyperplasia: a rare cause of primary aldosteronism |
title_fullStr |
Unilateral adrenal hyperplasia: a rare cause of primary aldosteronism |
title_full_unstemmed |
Unilateral adrenal hyperplasia: a rare cause of primary aldosteronism |
title_sort |
unilateral adrenal hyperplasia: a rare cause of primary aldosteronism |
publisher |
IIUM Press |
publishDate |
2021 |
url |
http://irep.iium.edu.my/91079/3/91079_Unilateral%20adrenal%20hyperplasia%20a%20rare%20cause%20of%20primary%20aldosteronism_SCOPUS.pdf http://irep.iium.edu.my/91079/4/91079_Unilateral%20adrenal%20hyperplasia%20a%20rare%20cause%20of%20primary%20aldosteronism.pdf http://irep.iium.edu.my/91079/ https://journals.iium.edu.my/kom/index.php/imjm/article/download/1449/1145/7618 https://doi.org/10.31436/imjm.v20i2.1449 |
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