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Peripheral primitive neuroectodermal tumor

ORPHA:370348· ICD-10 C71.9

Definition

A rare, aggressive, malignant, neoplastic disease characterized by a usually ill-defined, solid, multilobulated mass, frequently having necrosis, located on any site of the body (except the central nervous system), composed of small, round, poorly differentiated cells, with or without Homer-Wright rosettes, showing varying degrees of neuroectodermal differentiation. Manifestations are variable depending on location, with osteolytic destruction being common when arising from bone.

Prevalence
Unknown
Inheritance
Not applicable
Age of onset
Adolescent, Adult, Childhood