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dc.contributor.authorNath Adulkasemen_US
dc.contributor.authorDumnoensun Pruksakornen_US
dc.date.accessioned2019-08-05T04:40:51Z-
dc.date.available2019-08-05T04:40:51Z-
dc.date.issued2019-03-01en_US
dc.identifier.issn1757790Xen_US
dc.identifier.other2-s2.0-85063513764en_US
dc.identifier.other10.1136/bcr-2018-229076en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85063513764&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/65777-
dc.description.abstract© 2019 Author(s) (or their employer(s)). Re-use permitted under CC BY. Published by BMJ. Giant cell tumour (GCT) of bones in the hand is very rare, only 2% of all hand tumours, but unacceptably high recurrence rates (up to 90%) have been reported by several authors. Diagnosis can be challenging due to its rarity and enchondroma-mimicking characteristics. We report on a case of GCT of the middle phalanx of the left middle finger in a 49-year-old woman who underwent middle phalanx resection and reconstruction with bone grafting. At the 1-year follow-up, no evidence of recurrence was detected and the patient was pain-free.en_US
dc.subjectMedicineen_US
dc.titleGiant cell tumour of the middle phalanx of the middle fingeren_US
dc.typeJournalen_US
article.title.sourcetitleBMJ Case Reportsen_US
article.volume12en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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