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Synchronous multicentric giant cell tumour (GCT)-a rare case report

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dc.contributor.author Shekhar, Anshu
dc.contributor.author Murgod, Gururaj
dc.contributor.author Korlhalli, Suresh
dc.date.accessioned 2016-09-28T05:12:04Z
dc.date.available 2016-09-28T05:12:04Z
dc.date.issued 2014-02
dc.identifier.citation Journal of Clinical and Diagnostic Research. 2014 Feb; 8(2): 185-186. en_US
dc.identifier.issn 2249782X, 0973709X
dc.identifier.uri http://localhost:8080/xmlui/handle/123456789/809
dc.description.abstract Giant Cell Tumours (GCT) of bone account for 5% of all primary bone tumours. Multicentric variety is a rare variant of this condition, accounting for less than 1% of all cases and can occur as synchronous or metachronous lesions. We report a 22-year-old male patient with 18 months history of painful progressive swellings around the right knee. Radiographs revealed expansile lytic lesions in the distal femur, proximal tibia and fibula and core needle biopsy was typical of GCT. Biochemical parameters were normal and radiological investigations did not reveal any metastasis. The patient was treated by above knee amputation due to the extensive nature of the tumours. The excised tissue from all sites had features of giant cell tumor with no atypia or malignant cells seen. The patient is free from recurrence or metastasis at three years follow up. en_US
dc.language.iso en en_US
dc.publisher JCDR Research and Publications (Pvt) Limited en_US
dc.subject Giant cell tumour en_US
dc.subject Synchronous multicentric GCT en_US
dc.subject Osteoclastoma en_US
dc.title Synchronous multicentric giant cell tumour (GCT)-a rare case report en_US
dc.type Article en_US


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