Radiation-induced plexopathy
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
A rare radiation-induced disorder characterized by impairment of the peripheral nervous system at the level of the brachial or lumbosacral plexus following radiation therapy. Onset of symptoms can occur between several months up to decades after the last dose of radiation. Patients with radiation-induced brachial plexopathy typically present with mostly unilateral progressive paresthesia, followed by weakness, atrophy, and pain. Symptoms in radiation-induced lumbosacral plexopathy include more variable combinations of numbness, paresthesia, pain, and weakness, and are more often bilateral.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Radiation-induced plexopathy | |
| fr | Plexopathie radio-induite | |
| de | Strahleninduzierte Plexopathie | |
| es | Plexopatía inducida por radiación | |
| it | Plessopatia indotta dalle radiazioni | |
| nl | Stralingsgeïnduceerde plexopathie | Radiatiegeïnduceerde plexopathie |
| pt | Plexopatia induzida por radiação | |
| pl | Porażenie splotu nerwowego po radioterapii | |
| cs | Plexopatie vyvolaná radiací | |
| uk | Променева плексопатія | |
| zh | 辐射诱导的神经丛病 | |
| tr | Radyasyonla indüklenen pleksopati |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G54.0 | NTBT | attributed | not yet validated |
| ICD-11 | 8B91.Y | NTBT | index | validated |
| MONDO | 0033838 | E | validated | |
| UMLS | C5681446 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:182086Acquired peripheral neuropathy
rare neurological diseases - ORPHA:521132Radiation-induced disorder
rare disorders due to toxic effects
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/521123
- This record as JSON: /data/d/521123.json