peripheral primitive neuroectodermal tumor
MeSH: D018241ORPHA: 370348
Overview
small round cell tumor with neural differentiation arising from the soft tissues or bone
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with peripheral primitive neuroectodermal tumor, sourced from HPO and Orphanet clinical annotations.
Peripheral primitive neuroectodermal neoplasmTorticollisJaundicePruritusSeizureHyporeflexiaAscitesPancreatitisWeight lossAbnormal bleedingAnemiaAbnormal scalp morphologyNausea and vomitingAnorexiaHeadacheVertigoEpisodic abdominal painNeoplasm of the pancreasAbdominal distentionBack painSomatic sensory dysfunctionLower limb muscle weaknessSpinal cord tumorUterine neoplasmUpper limb painBrain neoplasmElevated circulating carcinoma antigen 125 concentrationPelvic massMetrorrhagiaOvarian neoplasmAbnormal thoracic spine morphologyProptosisPrecocious pubertyElevated circulating alpha-fetoprotein concentrationAbnormal superior cerebellar peduncle morphologyIncreased circulating lactate dehydrogenase concentrationNeoplasm of the scrotum
Classification & Codes
MeSH Code
D018241Orphanet Code
ORPHA:370348peripheral primitive neuroectodermal tumor
| MeSH | D018241 |
| Orphanet | ORPHA:370348 |
| Treatments | 0 drug(s) |
| Symptoms on record | 37 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO