Internal Medicine
Online ISSN : 1349-7235
Print ISSN : 0918-2918
ISSN-L : 0918-2918
CASE REPORTS
A Case of Primary Aldosteronism Caused by Multiple Adrenocortical Macronodules
Naoko HashimotoYoko KawamuraTomoaki NakamuraAyumi MurawakiTomoko NishiumiYushi HirotaKazuhiko SakagushiToshifumi KurahashiHideaki MiyakeMasato FujisawaHironobu SasanoYutaka Takahashi
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JOURNALS OPEN ACCESS

2011 Volume 50 Issue 6 Pages 585-590

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Abstract

A 60-year-old man presented with drug-resistant hypertension with hypokalemia, a high plasma aldosterone concentration (PAC) and suppressed plasma rennin activity (PRA). Imaging examinations showed multiple macronodules in the left adrenal gland. Endocrinological findings demonstrated autonomous aldosterone secretion and 131I-adosterol scintigraphy demonstrated a left sided uptake. Laparoscopic left adrenalectomy normalized serum potassium levels and PAC, and substantially improved hypertension. Pathological and immunohistochemical analysis demonstrated that these nodules were positive for 3β-hydroxysteroid dehydrogenase (HSD3B) but not for CYP17. In addition, zona glomerulosa demonstrated "paradoxical hyperplasia", in which these cells were negative for HSD3B. All of these data indicated that the nodules in the left adrenal gland were mainly responsible for the autonomous aldosterone secretion. We conclude that the primary aldosteronism in this case was caused by multiple macronodules. This is a very rare case of primary aldosteronism caused by multiple adrenocortical macronodules.

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© 2011 by The Japanese Society of Internal Medicine
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