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New insights into the medical management of primary aldosteronism.
Author(s) -
W A Hsueh
Publication year - 1986
Publication title -
hypertension
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.986
H-Index - 265
eISSN - 1524-4563
pISSN - 0194-911X
DOI - 10.1161/01.hyp.8.1.76
Subject(s) - primary aldosteronism , medicine , pheochromocytoma , secondary hypertension , hyperaldosteronism , aldosterone , urology , endocrinology , blood pressure
Case Presentation A 30-year-old woman was admitted to the hospital because of hypertension and hypokalemia. She had had a normal blood pressure measurement 5 years prior to admission and had been in good health until approximately 1 year before admission when a severe frontal headache and cramping in her hands and feet developed. She was seen in an emergency room and was noted to be hypertensive with a blood pressure of 170/100 mm Hg She was treated with methyldopa (Aldomet), and a blood sample analysis yielded the following values: serum sodium, 142 mEq/L; serum potassium, 2.2 mEq/L; CO2 level, 35 mEq/L; blood urea nitrogen, 13 mg/dl; and glucose, 91 mg/dl. Electrocardiogram (ECG) was normal except for the presence of U waves. An intravenous pyelogram was normal. While on the methyldopa regimen, the patient's headaches resolved; however, 9 months before admission, the patient discontinued all medications and her headaches returned. Three months before admission

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