Abstract |
The sequential occurrence of two primary bone tumors, Ewing's sarcoma and osteosarcoma in the same patient at two different anatomical sites 5 years apart is rare. We report a case of 12-year-old boy who after treatment for Ewing's sarcoma of proximal fibula subsequently presented, 4 years later, with a high-grade fibroblastic osteosarcoma of the proximal humerus. The patient was also found to have a rare gene tranlocation t (7;22) instead of the more common t (11;22).
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Authors | Vivek Sharma, Alvin H Crawford, Jonathan Evans, Margaret H Collins |
Journal | Journal of pediatric orthopedics. Part B
(J Pediatr Orthop B)
Vol. 17
Issue 6
Pg. 333-7
(Nov 2008)
ISSN: 1473-5865 [Electronic] United States |
PMID | 18841070
(Publication Type: Case Reports, Journal Article)
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Topics |
- Antineoplastic Combined Chemotherapy Protocols
(therapeutic use)
- Bone Neoplasms
(genetics, pathology, therapy)
- Child
- Chromosomes, Human, Pair 22
- Chromosomes, Human, Pair 7
- Combined Modality Therapy
- Fibula
(pathology)
- Humans
- Humerus
(pathology)
- Male
- Neoplasms, Second Primary
(genetics, pathology)
- Osteosarcoma
(genetics, pathology)
- Radiotherapy, Adjuvant
- Sarcoma, Ewing
(genetics, pathology, therapy)
- Translocation, Genetic
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