Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
2011-6-3
pubmed:abstractText
Pheochromocytomas are catecholamine producing tumors arising mostly from chromaffin cells of the adrenal medulla. The most common clinical presentation is hypertension, mainly in the form of paroxymal episodes. Cardiovascular manifestations include malignant arrhythmia and catecholamine cardiomyopathy, mimicking acute coronary syndromes and acute heart failure.There are reports of pheochromocytomas presenting as acute coronary syndrome and rapidly leading to cardiogenic shock; the failure of intensive medical treatment in these cases has prompted the need for emergency adrenalectomy as the only remaining option. We report on a case of complicated pheochromocytoma presenting as cardiogenic shock, in which emergency adrenalectomy was performed following a total lack of response to intensive medical treatment.
pubmed:commentsCorrections
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pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:issn
1477-7819
pubmed:author
pubmed:copyrightInfo
© 2011 Salinas et al; licensee BioMed Central Ltd.
pubmed:issnType
Electronic
pubmed:volume
9
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
49
pubmed:meshHeading
pubmed:year
2011
pubmed:articleTitle
Emergency adrenalectomy due to acute heart failure secondary to complicated pheochromocytoma: a case report.
pubmed:affiliation
General and Digestive Surgery Unit - Hospital Universitario Reina Sofía Córdoba, Spain. calesavera@hotmail.com
pubmed:publicationType
Journal Article, Case Reports