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dc.contributor.authorCamila B.R. De Mattosen_US
dc.contributor.authorChanika Angsanuntsukhen_US
dc.contributor.authorAlexandre Arkaderen_US
dc.contributor.authorJohn P. Dormansen_US
dc.contributor.otherThe Children's Hospital of Philadelphiaen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherChildren's Hospital Los Angelesen_US
dc.contributor.otherUniversity of Pennsylvaniaen_US
dc.identifier.citationJournal of the American Academy of Orthopaedic Surgeons. Vol.21, No.4 (2013), 225-233en_US
dc.description.abstractChondroblastoma and chondromyxoid fibroma are benign but locally aggressive bone tumors. Chondroblastoma, a destructive lesion with a thin radiodense border, is usually seen in the epiphysis of long bones. Chondromyxoid fibroma presents as a bigger, lucent, loculated lesion with a sharp sclerotic margin in the metaphysis of long bones. Although uncommon, these tumors can be challenging to manage. They share similarities in pathology that could be related to their histogenic similarity. Very rarely, chondroblastoma may lead to lung metastases; however, the mechanism is not well understood. Copyright 2013 by the American Academy of Orthopaedic Surgeons.en_US
dc.rightsMahidol Universityen_US
dc.titleChondroblastoma and chondromyxoid fibromaen_US
Appears in Collections:Scopus 2011-2015

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