| Literature DB >> 25800143 |
Philip C Johnston1, Amir H Hamrahian2, Robert J Weil3, Laurence Kennedy2.
Abstract
We review the etiology, investigations, management and outcomes of pituitary tumor apoplexy. Pituitary tumor apoplexy is a clinical syndrome which typically includes the acute onset of headache and/or visual disturbance, cranial nerve palsy and partial or complete endocrine dysfunction. It is associated with either infarction or hemorrhage of a pre-existing pituitary adenoma and is associated with significant morbidity and potential fatality. Not all patients will present with classic signs and symptoms, therefore it is pertinent to appreciate the clinical spectrum in which this condition can present.Entities:
Keywords: Apoplexy; Cranial nerve palsy; Hypopituitarism; Pituitary adenoma; Visual fields
Mesh:
Year: 2015 PMID: 25800143 DOI: 10.1016/j.jocn.2014.11.023
Source DB: PubMed Journal: J Clin Neurosci ISSN: 0967-5868 Impact factor: 1.961