Secondary Chondrosarcoma
Secondary Chondrosarcoma
Secondary Chondrosarcoma
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Patrick P. Lin, MD, et al<br />
<strong>Chondrosarcoma</strong>, in Fletcher CDM,<br />
Unni KK, Mertens F, eds: World Health<br />
Organization Classification of Tumours:<br />
Pathology & Genetics: Tumours of Soft<br />
Tissue and Bone. Lyon, France, IARC<br />
Press, 2002, pp 247-251.<br />
21. Huvos AG: Solitary and multiple<br />
osteochondromas and enchondromas,<br />
juxtacortical chondroma, Mafucci’s<br />
disease, in Huvos AG, ed: Bone Tumors:<br />
Diagnosis, Treatment and Prognosis.<br />
Philadelphia, PA, WB Saunders<br />
Company, 1991, pp 253-294.<br />
22. Spjut HJ, Dorfman HD, Fechner RE,<br />
Ackerman LV: Tumors of cartilaginous<br />
origin, in Firminger HI, ed: Atlas of<br />
Tumor Pathology, Second Series, Fascicle<br />
5: Tumors of Bone and Cartilage.<br />
Washington, DC, Armed Forces Institute<br />
of Pathology, 1971, pp 33-116.<br />
23. Forest M: Osteochondroma, in Forest<br />
M, Tomeno B, Vanel D, eds: Orthopedic<br />
Surgical Pathology: Diagnosis of Tumors<br />
and Pseudotumoral Lesions of Bone and<br />
Joints. Edinburgh, Scotland, Churchill<br />
Livingstone, 1998, pp 117-190.<br />
24. Eefting D, Schrage YM, Geirnaerdt MJ,<br />
et al: Assessment of interobserver<br />
variability and histologic parameters to<br />
improve reliability in classification and<br />
grading of central cartilaginous tumors.<br />
Am J Surg Pathol 2009;33(1):50-57.<br />
25. Flemming DJ, Murphey MD:<br />
Enchondroma and chondrosarcoma.<br />
Semin Musculoskelet Radiol 2000;4(1):<br />
59-71.<br />
26. Campanacci M: Multiple chondromas<br />
(chondromatosis, Ollier’s disease,<br />
Maffucci’s syndrome), in Campanacci<br />
M: Bone and Soft Tissue Tumors, ed2.<br />
New York, NY, Springer, 1999, pp 235-<br />
245.<br />
27. Mirra JM: The osteochondroma, solitary<br />
and multiple, in Mirra JM, ed: Bone<br />
Tumors: Diagnosis and Treatment.<br />
Philadelphia, PA, JB Lippincott, 1980,<br />
pp 520-532.<br />
28. O’Neal LW, Ackerman LV: <strong>Chondrosarcoma</strong><br />
of bone. Cancer 1952;5(3):551-<br />
577.<br />
29. Cook A, Raskind W, Blanton SH, et al:<br />
Genetic heterogeneity in families with<br />
hereditary multiple exostoses. Am J Hum<br />
Genet 1993;53(1):71-79.<br />
30. Wu YQ, Heutink P, de Vries BB, et al:<br />
Assignment of a second locus for<br />
multiple exostoses to the pericentromeric<br />
region of chromosome 11. Hum Mol<br />
Genet 1994;3(1):167-171.<br />
31. Le Merrer M, Legeai-Mallet L, Jeannin<br />
PM, et al: A gene for hereditary multiple<br />
exostoses maps to chromosome 19p.<br />
Hum Mol Genet 1994;3(5):717-722.<br />
32. Porter DE, Lonie L, Fraser M, et al:<br />
Severity of disease and risk of malignant<br />
change in hereditary multiple exostoses:<br />
A genotype-phenotype study. J Bone<br />
Joint Surg Br 2004;86(7):1041-1046.<br />
33. Wuyts W, Van Hul W, De Boulle K,<br />
et al: Mutations in the EXT1 and EXT2<br />
genes in hereditary multiple exostoses.<br />
Am J Hum Genet 1998;62(2):346-354.<br />
34. Bovée JV, Cleton-Jansen AM, Wuyts W,<br />
et al: EXT-mutation analysis and loss of<br />
heterozygosity in sporadic and hereditary<br />
osteochondromas and secondary<br />
chondrosarcomas. Am J Hum Genet<br />
1999;65(3):689-698.<br />
35. Schwartz HS, Zimmerman NB, Simon<br />
MA, Wroble RR, Millar EA, Bonfiglio<br />
M: The malignant potential of<br />
enchondromatosis. J Bone Joint Surg Am<br />
1987;69(2):269-274.<br />
36. Lewis RJ, Ketcham AS: Maffucci’s<br />
syndrome: Functional and neoplastic<br />
significance. Case report and review of<br />
the literature. J Bone Joint Surg Am<br />
1973;55(7):1465-1479.<br />
37. Hopyan S, Gokgoz N, Poon R, et al: A<br />
mutant PTH/PTHrP type I receptor in<br />
enchondromatosis. Nat Genet 2002;<br />
30(3):306-310.<br />
38. Rozeman LB, Sangiorgi L, Briaire-de<br />
Bruijn IH, et al: Enchondromatosis<br />
(Ollier disease, Maffucci syndrome) is<br />
not caused by the PTHR1 mutation<br />
p.R150C. Hum Mutat 2004;24(6):466-<br />
473.<br />
39. Florez B, Mönckeberg J, Castillo G,<br />
Beguiristain J: Solitary osteochondroma<br />
long-term follow-up. J Pediatr Orthop B<br />
2008;17(2):91-94.<br />
40. Schmale GA, Conrad EU III, Raskind<br />
WH: The natural history of hereditary<br />
multiple exostoses. J Bone Joint Surg Am<br />
1994;76(7):986-992.<br />
41. Wicklund CL, Pauli RM, Johnston D,<br />
Hecht JT: Natural history study of<br />
hereditary multiple exostoses. Am J Med<br />
Genet 1995;55(1):43-46.<br />
42. Murphey MD, Choi JJ, Kransdorf MJ,<br />
Flemming DJ, Gannon FH: Imaging of<br />
osteochondroma: Variants and<br />
complications with radiologic-pathologic<br />
correlation. Radiographics 2000;20(5):<br />
1407-1434.<br />
43. Pierz KA, Womer RB, Dormans JP:<br />
Pediatric bone tumors: Osteosarcoma<br />
ewing’s sarcoma, and chondrosarcoma<br />
associated with multiple hereditary<br />
osteochondromatosis. J Pediatr Orthop<br />
2001;21(3):412-418.<br />
44. Schwab JH, Wenger D, Unni K, Sim FH:<br />
Does local recurrence impact survival in<br />
low-grade chondrosarcoma of the long<br />
bones? Clin Orthop Relat Res 2007;462:<br />
175-180.<br />
45. Weber KL, Pring ME, Sim FH:<br />
Treatment and outcome of recurrent<br />
pelvic chondrosarcoma. Clin Orthop<br />
Relat Res 2002;397:19-28.<br />
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