[Rhabdomyosarcoma in childhood. II. Ultrastructure]. 1985

R Kodet

The diagnosis of rhabdomyosarcoma was established or proved by electron microscopy in two thirds of 21 cases. Histological classification was not adequate or formulated as "undifferentiated sarcoma" in half the cases. Electron microscopy did not succeed in one third of cases and rhabdomyosarcoma was classified according to simultaneous or successive study. Undifferentiated tumour cells resembled myoblastema cells of the 5th-6th gestation weeks. Differentiation of myoblasts and myotubes corresponded to the muscle development of the 7th-16th weeks. Immature cells showed features of fibroblasts and myofibroblasts in most cases of embryonal rhabdomyosarcoma. Alveolar rhabdomyosarcomas were characterized by exclusive myoblastic differentiation. Different cellular sources were discussed in rhabdomyosarcomas with differentiation into one cell type or into various mesenchymal cells.

UI MeSH Term Description Entries
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D012208 Rhabdomyosarcoma A malignant solid tumor arising from mesenchymal tissues which normally differentiate to form striated muscle. It can occur in a wide variety of sites. It is divided into four distinct types: pleomorphic, predominantly in male adults; alveolar (RHABDOMYOSARCOMA, ALVEOLAR), mainly in adolescents and young adults; embryonal (RHABDOMYOSARCOMA, EMBRYONAL), predominantly in infants and children; and botryoidal, also in young children. It is one of the most frequently occurring soft tissue sarcomas and the most common in children under 15. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p2186; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1647-9) Rhabdomyosarcomas

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