Pediatric bone tumors: Osteosarcoma, Ewing's sarcoma, and chondrosarcoma associated with multiple hereditary osteochondromatosis

Journal of Pediatric Orthopaedics

Volumn 21, Issue 3, 2001, Pages 412-418

  Pierz, Kristan A ^a   Womer, Richard B ^a,b   Dormans, John P ^a,b   Stanitski, Carl L ^c  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c Wood Bldg ^*

Author keywords

[No Author keywords available]

Indexed keywords

CISPLATIN; DOXORUBICIN; GRANULOCYTE COLONY STIMULATING FACTOR; IFOSFAMIDE; METHOTREXATE;

ARTICLE; BONE BIOPSY; BONE RADIOGRAPHY; BONE TUMOR; CANCER INCIDENCE; CANCER RISK; CANCER SURVIVAL; CHILDHOOD CANCER; CHONDROSARCOMA; CLINICAL FEATURE; EWING SARCOMA; MALIGNANT TRANSFORMATION; OSTEOCHONDROMA; OSTEOSARCOMA; PRIORITY JOURNAL; PROGNOSIS;

EID: 0035032018     PISSN: 02716798     EISSN: None     Source Type: Journal    
DOI: 10.1097/01241398-200105000-00028     Document Type: Article

References (70)

1. Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXTI)
2. Massive allografts in the treatment of osteosarcoma and Ewing sarcoma in children and adolescents
3. Two primary osteosarcomas in a patient with Rothmund-Thomson syndrome
4. Common musculoskeletal tumors of childhood and adolescence
5. Extensible endoprostheses of the humerus after resection of bone tumours
6. Prognostic factors in nonmetastatic Ewing's sarcoma of bone treated with adjuvant chemotherapy: Analysis of 359 patients at the Istituto Ortopedico Rizzoli
7. Molecular assays for chromosomal translocations in the diagnosis of pediatric soft tissue sarcomas
8. Multimodal therapy for the management of nonpelvic, localized Ewing's sarcoma of bone: Intergroup study IESS-II
9. Proximal fibular osteochondroma with associated peroneal nerve palsy: A review of six cases
10. Clinical correlation to genetic variations of hereditary multiple exostosis
11. Current combined treatment of high-grade osteosarcomas
12. Functional outcome in amputation versus limb sparing of patients with lower extremity sarcoma: A matched case-control study
13. Prognostic impact of p53 status in Ewing sarcoma
14. Bone cancers
15. Expandable endoprosthesis reconstruction in skeletally immature patients with tumors
16. A system for the surgical staging of musculoskeletal sarcoma
17. Bone scintigraphy in hereditary multiple exostoses
18. Acetabular dysplasia associated with hereditary multiple exostoses. A case report
19. Ewing sarcoma of the pelvis
20. Chondrosarcoma arising in osteochondroma
21. Molecular biology of sarcomas
22. Incidence of cancer in children in the United States
23. Malignant bone tumors
24. Primary bone malignancies in children
25. Hereditary multiple exostosis and chondrosarcoma: Linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8
26. Childhood tumors
27. Malignant bone tumors of childhood
28. Scintigraphy of benign exostoses and exostotic chondrosarcomas
29. Correlative radiographic, scintigraphic, and histological evaluation of exostoses
30. Targeting tumor specific translocations in sarcomas in pediatric patients for immunotherapy
31. Benign osteochondromas and exostotic chondrosarcomas: Evaluation of cartilage cap thickness by ultrasound
32. The hazards of biopsy in patients with malignant primary bone and soft-tissue tumors
33. The Ewing's sarcoma EWS/FLI- I fusion gene encodes a more potent transcriptional activator and is a more powerful transforming gene than FLI-I
34. Germline mutations of the p53 tumor suppressor gene in children with osteosarcoma
35. Musculoskeletal tumors of childhood
36. Differential diagnosis of pediatric musculoskeletal masses
37. Osteogenic sarcoma with clinically detectable metastasis at initial presentation
38. Imaging of osteochondroma: Variants and complications with radiologic-pathologic correlation
39. Making the diagnosis - Keys to a successful biopsy in children with bone and soft-tissue tumors
40. Multiple hereditary osteochondromata
41. Prognostic factors among 130 patients with osteosarcoma
42. The neoplastic pathogenesis of solitary and multiple osteochondromas
43. Prognostic indicators in patients with pulmonary metastases
44. Radiologic and pathologic analysis of solitary bone lesions
45. Thallium-201 scintigraphy in bone sarcoma: Comparison with gallium-67 and technetium-MDP in the evaluation of chemotherapeutic response
46. Italian cooperative study for the treatment of children and young adults with localized Ewing sarcoma of bone - A preliminary report of 6 years of experience
47. Pediatric cancer in the United States
48. Chemotherapy in osteosarcoma - The Scandinavian Sarcoma Group experience
49. Fine needle aspiration cytology of the Ewing's sarcoma family of tumors
50. The natural history of hereditary multiple exostoses
51. Hereditary multiple exostoses
52. Tumor volume change as a predictor of chemotherapeutic response in osteosarcoma
53. The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes
54. Chromosomal regions involved in the pathogenesis of osteosarcomas
55. A practical classification system for multiple cartilaginous exostosis in children
56. Total en bloc spondylectomy. A new surgical technique for primary malignant vertebral tumors
57. Antibodies to heat shock protein 90 in osteosarcoma patients correlate with response to neoadjuvant chemotherapy
58. Marginal excision for osteosarcoma with caffeine assisted chemotherapy
59. Mutation spectrum of the retinoblastoma gene in osteosarcoma
60. Fine needle aspiration biopsy of primary bone tumors
61. Prognostic impact of INK4A deletion in Ewing sarcoma
62. The success of limb-salvage surgery in the adolescent patient with osteogenic sarcoma
63. Initial symptoms and clinical features in osteosarcoma and Ewing sarcoma
64. Malignant transformation of a multiple cartilaginous exostosis - A case report
65. Surgical risk for elective excision of benign exostoses
66. Secondary chondrosarcoma in osteochondromas. Medullary extension in 15 of 45 cases
67. Chondrosarcoma of bone in children