About: Alveolar Rhabdomyosarcoma     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Alveolar Rhabdomyosarcoma
equivalentClass
Concept_In_Subset
Semantic_Type
  • Neoplastic Process
Preferred_Name
  • Alveolar Rhabdomyosarcoma
UMLS_CUI
  • C0206655
Contributing_Source
  • CTEP
ALT_DEFINITION
  • A soft tissue tumor that is most common in older children and teenagers. It begins in embryonic muscle cells (cells that develop into muscles in the body). It can occur at many places in the body, but usually occurs in the trunk, arms, or legs.NCI-GLOSS
  • A primitive, malignant round cell neoplasm that cytologically resembles lymphoma and which shows partial skeletal muscle differentiation. Recurrent cytogenetic aberrations are specifically associated with this entity: t(2;13)(q35;q14) and t(1;13)(p36;q14).NCI
ICD-O-3_Code
  • 8920/3
Neoplastic_Status
  • Malignant
Legacy_Concept_Name
  • Alveolar_Rhabdomyosarcoma
FULL_SYN
  • ARMSPTNCI-GLOSSCDR0000641928
  • alveolar rhabdomyosarcomaPTNCI-GLOSSCDR0000641927
  • Alveolar RhabdomyosarcomaPTNCI
  • Alveolar rhabdomyosarcomaPTCTEP10065867
DEFINITION
  • A rapidly growing malignant mesenchymal neoplasm. It is characterized by the presence of round cells with myoblastic differentiation and a fibrovascular stroma resembling an alveolar growth pattern. The tumor usually presents in the extremities.NCI
code
  • C3749
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