Familial chordoma. A report of two cases.

نویسندگان

  • A K Bhadra
  • A T H Casey
چکیده

We have treated 175 patients with a chordoma over a ten-year period. Only two had a family history of the condition and we describe these in this paper. In one patient the tumour was at the craniocervical junction and in the other the lesion affected the sacrum. We have undertaken a literature review of familial chordoma and have identified chromosomal abnormalities associated with the condition.

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عنوان ژورنال:
  • The Journal of bone and joint surgery. British volume

دوره 88 5  شماره 

صفحات  -

تاریخ انتشار 2006