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Rhabdomyosarcoma an ubiquitous pediatric tumour.

Abstract
Rhabdomyosarcoma is the most common soft tissue tumor in children. It occurs everywhere and its prognosis depends on the location and its histological type--embryonic or alveolar. The new immunohistochemical markers desmin and myogenin in combination with molecular biological detection of specific translocations in alveolar rhabdomyosarcoma improved diagnostic capacities. Less aggressive treatment in curable cases reduces the undesirable outcomes of therapy.
AuthorsV Verkarre, L Galmiche-Rolland, S Sarnacki, F Jaubert
JournalArkhiv patologii (Arkh Patol) 2008 May-Jun Vol. 70 Issue 3 Pg. 50-3 ISSN: 0004-1955 [Print] Russia (Federation)
PMID18727437 (Publication Type: Lecture)
Topics
  • Cell Differentiation
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Muscle, Skeletal
  • Rhabdomyosarcoma (diagnosis, metabolism, pathology, therapy)

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