Chondroblastoma in distal femur

Chondroblastoma was first described in detail by codman in 1931 and so is occasionally referred to as codman’s tumor. Chondroblastoma is a rare primary benign bone tumor arising from immature cells of epiphyseal cartilage with preferential localization in the epiphysis or apophysis. Onset occur...

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প্রধান লেখক: R Karthik Reddy1 , M Nagendra Babu2 , J Mothilal3 , P Saiprashanth Reddy4
বিন্যাস: প্রবন্ধ
ভাষা:English
প্রকাশিত: Prathima Institute of Medical Sciences 2017-12-01
মালা:Perspectives In Medical Research
বিষয়গুলি:
অনলাইন ব্যবহার করুন:http://www.pimr.org.in/karthikreddy_vol5-issue3-2017.PDF
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author R Karthik Reddy1 , M Nagendra Babu2 , J Mothilal3 , P Saiprashanth Reddy4
author_facet R Karthik Reddy1 , M Nagendra Babu2 , J Mothilal3 , P Saiprashanth Reddy4
author_sort R Karthik Reddy1 , M Nagendra Babu2 , J Mothilal3 , P Saiprashanth Reddy4
collection DOAJ
description Chondroblastoma was first described in detail by codman in 1931 and so is occasionally referred to as codman’s tumor. Chondroblastoma is a rare primary benign bone tumor arising from immature cells of epiphyseal cartilage with preferential localization in the epiphysis or apophysis. Onset occurs before obliteration of the ephiphyseal line, from 10 to 20 years of age. Males predominate with a ratio of 3 to 2. Chondroblastomas are generally treated by curettage with or without bone grafts. In this report, our aim was to present a rare tumor chondroblastoma which was localized in the distal femoral epiphysis
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spelling doaj.art-0f1d2e0da4954386a10923fb5b902ed92023-11-24T11:52:43ZengPrathima Institute of Medical SciencesPerspectives In Medical Research2348-14472348-229X2017-12-01537476Chondroblastoma in distal femurR Karthik Reddy1 , M Nagendra Babu2 , J Mothilal3 , P Saiprashanth Reddy40 Prathima Insitute of Medical SciencesChondroblastoma was first described in detail by codman in 1931 and so is occasionally referred to as codman’s tumor. Chondroblastoma is a rare primary benign bone tumor arising from immature cells of epiphyseal cartilage with preferential localization in the epiphysis or apophysis. Onset occurs before obliteration of the ephiphyseal line, from 10 to 20 years of age. Males predominate with a ratio of 3 to 2. Chondroblastomas are generally treated by curettage with or without bone grafts. In this report, our aim was to present a rare tumor chondroblastoma which was localized in the distal femoral epiphysishttp://www.pimr.org.in/karthikreddy_vol5-issue3-2017.PDFchondroblastomaepiphyseal tumourcurettage
spellingShingle R Karthik Reddy1 , M Nagendra Babu2 , J Mothilal3 , P Saiprashanth Reddy4
Chondroblastoma in distal femur
Perspectives In Medical Research
chondroblastoma
epiphyseal tumour
curettage
title Chondroblastoma in distal femur
title_full Chondroblastoma in distal femur
title_fullStr Chondroblastoma in distal femur
title_full_unstemmed Chondroblastoma in distal femur
title_short Chondroblastoma in distal femur
title_sort chondroblastoma in distal femur
topic chondroblastoma
epiphyseal tumour
curettage
url http://www.pimr.org.in/karthikreddy_vol5-issue3-2017.PDF
work_keys_str_mv AT rkarthikreddy1mnagendrababu2jmothilal3psaiprashanthreddy4 chondroblastomaindistalfemur