Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1998-10-29
pubmed:abstractText
INTRODUCTION: Primary hyperaldosteronism is an uncommon cause of hypertension which classically features hypokaliemia, metabolic alkalosis and excessive urinary potassium excretion. Clinical manifestations of hypokalemia rarely reveal the diagnosis. EXEGESE: We report the case of a hypertensive patient who developed quadriparesis and rhabdomyolysis induced by a severe hypokalemia. Clinical manifestations were reversible after potassium supplementation. Laboratory and radiological findings led to the diagnosis of an aldosterone-producing adenoma. Surgical treatment allowed correction of electrolyte abnormalities and improvement of hypertension. CONCLUSION: Although primary aldosteronism is rare, it should be systematically considered when arterial hypertension is associated with hypokalemia, even if the potassium depletion is due to diuretic therapy.
pubmed:language
fre
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0248-8663
pubmed:author
pubmed:issnType
Print
pubmed:volume
19
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
203-5
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed:year
1998
pubmed:articleTitle
[Conn adenoma manifesting as reversible tetraparesis and rhabdomyolysis].
pubmed:affiliation
Service de médecine interne, hôpital Broussais, Paris, France.
pubmed:publicationType
Journal Article, English Abstract, Case Reports