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Granulomatous hypophysitis: rare disease with challenging diagnosis

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dc.contributor.authorElgamal, Mohannad Essam
dc.date.accessioned2021-03-01T08:14:48Z
dc.date.available2021-03-01T08:14:48Z
dc.date.issued2017
dc.description.abstractAbstract: Granulomatous hypophysitis is rare pathology that mimics pituitary adenoma. Diagnosis is only confirmed by histopathology examination. Trans-sphenoidal surgery is considered diagnostic when descent tissue specimen is obtained and therapeutic by decompressing optic pathway and the sella. Pathological findings always reveal granulomatous areas, multinucleated giant cells, plasma cells, and lymphocytes.en_US
dc.identifier.other204-2017.19
dc.identifier.urihttps://repository.mbru.ac.ae/handle/1/175
dc.language.isoenen_US
dc.subjectDiabetes insipidusen_US
dc.subjectGranulomatous hypophysitisen_US
dc.subjectPituitary adenomaen_US
dc.subjectTranssphenoidal surgeryen_US
dc.subjectVisual field defecten_US
dc.titleGranulomatous hypophysitis: rare disease with challenging diagnosisen_US
dc.typeArticleen_US
dspace.entity.typePublicationen_US

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