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dc.contributor.authorPourfeizi, HH
dc.contributor.authorTabrizi, A
dc.contributor.authorTaleb, H
dc.contributor.authorBazavar, M
dc.date.accessioned2018-08-26T08:56:19Z
dc.date.available2018-08-26T08:56:19Z
dc.date.issued2013
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/54427
dc.description.abstractPrimary hyperparathyroidism is a rare endocrine disease characterized by hypersecretion of parathormone. Giant cell tumor (GCT) of bone arising from a finger phalanx is an extremely rare phenomenon. We introduced patients with tumoral mass in the fifth proximal phalanx of their right hand. Although pathology findings indicated to giant cell tumor, she had hyperparathyroid adenoma and treated by parathyroidectomy. Neoplastic lesions gradually disappeared without further surgical interventions.
dc.language.isoEnglish
dc.relation.ispartofShiraz E Medical Journal
dc.subjectalkaline phosphatase
dc.subjectcalcium
dc.subjectparathyroid hormone
dc.subjectphosphate
dc.subjectadult
dc.subjectarticle
dc.subjectbiopsy
dc.subjectbone radiography
dc.subjectcase report
dc.subjectfemale
dc.subjecthistology
dc.subjecthuman
dc.subjecthuman tissue
dc.subjectosteoclastoma
dc.subjectparathyroid adenoma
dc.subjectparathyroidectomy
dc.subjectphalanx
dc.subjectphysical examination
dc.subjectwhole body scintiscanning
dc.titleGiant cell tumor or brown tumor of a phalanx in the hand: A case report in a 44-year-old woman
dc.typeArticle
dc.citation.volume14
dc.citation.issue2
dc.citation.indexScopus


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