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Chondrosarcoma
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==Types== {| class="wikitable" |+Table 1: Types of chondrosarcoma |- valign=top ! ! <u>Subtype</u> ! Percentage of cases % |- valign=top | rowspan="3" | '''Conventional''' | Primary central | ~75%<ref name=":0">{{Cite journal|last1=Gelderblom|first1=Hans|last2=Hogendoorn|first2=Pancras C. W.|last3=Dijkstra|first3=Sander D.|last4=van Rijswijk|first4=Carla S.|last5=Krol|first5=Augustinus D.|last6=Taminiau|first6=Antonie H. M.|last7=BovΓ©e|first7=Judith V. M. G.|date=March 2008|title=The clinical approach towards chondrosarcoma|journal=The Oncologist|volume=13|issue=3|pages=320β329|doi=10.1634/theoncologist.2007-0237|issn=1083-7159|pmid=18378543|s2cid=20484590 |doi-access=free}}</ref> |- |Secondary peripheral |~10%<ref name=":0" /> |- valign="TOP" | Periosteal (aka juxtacortical)<ref>{{Cite journal|last=Schajowicz|first=F.|date=November 1977|title=Juxtacortical chondrosarcoma|journal=The Journal of Bone and Joint Surgery. British Volume|volume=59-B|issue=4|pages=473β480|doi=10.1302/0301-620X.59B4.270475|issn=0301-620X|pmid=270475|doi-access=free}}</ref><ref name=":1">{{Cite book|url=https://www.worldcat.org/oclc/51001831|title=Pathology and genetics of tumours of soft tissue and bone|date=2002|publisher=IARC Press|others=Fletcher, Christopher D. M., Unni, K. Krishnan, 1941β, Mertens, Fredrik., World Health Organization., International Agency for Research on Cancer.|isbn=978-92-832-2413-6|location=Lyon|oclc=51001831}}</ref> | <1%<ref name=":0" /> |- valign="top" | rowspan="3" |'''Rare''' | Dedifferentiated | valign="bottom" | ~10%<ref name=":0" /> |- valign="top" | Mesenchymal | ~2%<ref name=":0" /> |- valign="TOP" | Clear-cell | ~2%<ref name=":1" /> |}
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