This Article
Right arrow Full Text (PDF)
Right arrow Letters to the Editor: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Letters to the Editor are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My File Cabinet
Right arrow Download to citation manager
Right arrowReprints and Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Samson, I. R.
Right arrow Articles by Mankin, H. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Samson, I. R.
Right arrow Articles by Mankin, H. J.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Technorati  
What's this?

The Journal of Bone and Joint Surgery, Vol 75, Issue 10 1476-1484, Copyright © 1993 by Journal of Bone and Joint Surgery, Inc


JOURNAL CONTENTS

Operative treatment of sacrococcygeal chordoma. A review of twenty-one cases

IR Samson, DS Springfield, HD Suit and HJ Mankin
Orthopaedic Oncology Unit, Massachusetts General Hospital, Boston 02114.

Between 1972 and 1992, twenty-one patients had a primary operation for the treatment of a sacrococcygeal chordoma; seventeen had had a diagnostic biopsy elsewhere. The average age at the time of the operation was fifty-five years (range, six to seventy-eight years); fourteen patients were male and seven were female. In all patients, a posterior approach was used, even for resections at the cephalic levels of the sacrum. In addition, sixteen of the twenty-one patients were treated with adjuvant radiation therapy. Four patients died; three died of metastatic chordoma. Of the remaining seventeen patients, fifteen were apparently free of disease and had not had a local recurrence at the time of the latest follow-up examination. The average duration of follow-up for these fifteen patients was four and one-half years. Of the nine patients who were followed for at least five years, seven were disease-free at the latest follow-up evaluation. Of the seven patients in whom both second sacral roots were the most caudad nerve-roots spared, four had normal bladder control and five had normal bowel control. Of the four patients in whom the most caudad nerve-roots spared were the first sacral or more cephalic roots, all had impaired bladder control, one had impaired bowel control, and three had a colostomy.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
JBJSHome page
C. A. Hulen, H. T. Temple, W. P. Fox, A. A. Sama, B. A. Green, and F. J. Eismont
Oncologic and Functional Outcome Following Sacrectomy for Sacral Chordoma
J. Bone Joint Surg. Am., July 1, 2006; 88(7): 1532 - 1539.
[Abstract] [Full Text] [PDF]


Home page
JBJSHome page
B. Fuchs, I. D. Dickey, M. J. Yaszemski, C. Y. Inwards, and F. H. Sim
Operative Management of Sacral Chordoma
J. Bone Joint Surg. Am., October 1, 2005; 87(10): 2211 - 2216.
[Abstract] [Full Text] [PDF]


Home page
Clin. Cancer Res.Home page
R. Imai, T. Kamada, H. Tsuji, T. Yanagi, M. Baba, T. Miyamoto, S. Kato, S. Kandatsu, J.-e. Mizoe, H. Tsujii, et al.
Carbon Ion Radiotherapy for Unresectable Sacral Chordomas
Clin. Cancer Res., September 1, 2004; 10(17): 5741 - 5746.
[Abstract] [Full Text] [PDF]


Home page
Ann. Surg. Oncol.Home page
D. Baratti, A. Gronchi, E. Pennacchioli, L. Lozza, M. Colecchia, M. Fiore, and M. Santinami
Chordoma: Natural History and Results in 28 Patients Treated at a Single Institution
Ann. Surg. Oncol., April 1, 2003; 10(3): 291 - 296.
[Abstract] [Full Text] [PDF]


Home page
JBJSHome page
D. A. SPIEGEL, W. J. RICHARDSON, S. P. SCULLY, and J. M. HARRELSON
Long-Term Survival Following Total Sacrectomy with Reconstruction for the Treatment of Primary Osteosarcoma of the Sacrum. A Case Report
J. Bone Joint Surg. Am., June 1, 1999; 81(6): 848 - 55.
[Full Text]