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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Nath Adulkasem | en_US |
dc.contributor.author | Dumnoensun Pruksakorn | en_US |
dc.date.accessioned | 2019-08-05T04:40:51Z | - |
dc.date.available | 2019-08-05T04:40:51Z | - |
dc.date.issued | 2019-03-01 | en_US |
dc.identifier.issn | 1757790X | en_US |
dc.identifier.other | 2-s2.0-85063513764 | en_US |
dc.identifier.other | 10.1136/bcr-2018-229076 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85063513764&origin=inward | en_US |
dc.identifier.uri | http://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.subject | Medicine | en_US |
dc.title | Giant cell tumour of the middle phalanx of the middle finger | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | BMJ Case Reports | en_US |
article.volume | 12 | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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