Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/10065
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dc.contributor.authorRistevska, Nevenaen_US
dc.contributor.authorStojanoski, Sinisaen_US
dc.contributor.authorPop Gjorcheva, Danielaen_US
dc.contributor.authorAngjeleska Merien_US
dc.date.accessioned2021-02-12T12:43:37Z-
dc.date.available2021-02-12T12:43:37Z-
dc.date.issued2015-06-04-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/10065-
dc.description.abstractOsteitis fibrosa cystica is the classic patognomonic form of skeletal disease in hyperparathyroidism that characterizes with decreased cortical bone thickness compared to increased cancellous bone. We present a case of 52-year old female patient with osteolysis of the left calf on radiographic images. The bone scan detected multiple focal pathological accumulations in the skull, left tibia, both femurs and in the left ischium. The scan was indicative of secondary multiple skeletal metastases. Because the patient had no previous history of primary malignant disease, metabolic bone disease was suspected and also confirmed after i.v application of 99mTc-MIBI. The scan was in favor of parathyroid adenoma with bone complication (osteitis fibrosa cystica). Neck ultrasonography revealed hypoechoic oval mass below the left lower thyroid lobe that suggested the possibility of parathyroid adenoma. An increased ionized calcium level and PTH confirmed the diagnosis of primary hyperparathyroidism. Parathyroidectomy with radioguided surgery was performed. Hyperparathyroidism is a curable disease and a clinician should always bear in mind a metabolic bone disease when performing a nuclear bone scan where multiple bone lesions are detected (a hallmark of metastatic disease).en_US
dc.language.isoenen_US
dc.relation.ispartofIranian Journal of Nuclear Medicineen_US
dc.subjectparathyroid adenomaen_US
dc.subject99mTc-MIBIen_US
dc.subjectscintigraphyen_US
dc.subjectPTHen_US
dc.titleScintigraphic evaluation of multifocal osteolytic lesions in a patient with primary hyperparathyroidism: A case reporten_US
dc.typeArticleen_US
item.grantfulltextnone-
item.fulltextNo Fulltext-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
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