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10.1308/rcsann.2016.0138

http://scihub22266oqcxt.onion/10.1308/rcsann.2016.0138
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27087325/?report=reader!5227051!27087325
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suck abstract from ncbi

pmid27087325      Ann+R+Coll+Surg+Engl 2016 ; 98 (5): 324-8
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  • Extra-axial chordomas #MMPMID27087325
  • Evans S; Khan Z; Jeys L; Grimer R
  • Ann R Coll Surg Engl 2016[May]; 98 (5): 324-8 PMID27087325show ga
  • INTRODUCTION: A chordoma is a slow growing malignant tumour of notochordal origin. A tumour with histological features that are identical to those of a chordoma may arise outside the axial skeleton. To date, there is little in the literature documenting their clinical course. METHODS: Our large orthopaedic oncology database was used to document the clinical course of extra-axial chordoma. RESULTS: Over a 30-year period, 131 patients diagnosed with a chordoma were treated at our unit. Only three (2.3%) of these cases were extra-axial chordomas: one in the femur, one in the ulna and one in the proximal fibula. All underwent surgical resection. CONCLUSIONS: In view of the rarity of this tumour and the difficulty in confirming its diagnosis, we suggest that any suspected case is discussed with a specialist sarcoma multidisciplinary team so that the correct diagnosis can be achieved and treatment tailored accordingly.
  • |*Bone Neoplasms[MESH]
  • |*Chordoma[MESH]
  • |Adult[MESH]
  • |Aged[MESH]
  • |Fibula/diagnostic imaging/pathology[MESH]
  • |Humans[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Radiography[MESH]


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