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Sequential Ewing's sarcoma and osteosarcoma.

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).
AuthorsVivek Sharma, Alvin H Crawford, Jonathan Evans, Margaret H Collins
JournalJournal of pediatric orthopedics. Part B (J Pediatr Orthop B) Vol. 17 Issue 6 Pg. 333-7 (Nov 2008) ISSN: 1473-5865 [Electronic] United States
PMID18841070 (Publication Type: Case Reports, Journal Article)
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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