Lichen amyloidosis
Synonyms: Amyloid lichen · Lichen amyloidosus
- Type
- Disease
- Group
- Disorder
- Age of onset
- Adolescent, Adult
- Status
- active
Lichen amyloidosis is a rare chronic form of cutaneous amyloidosis, a skin disease characterized by the accumulation of amyloid deposits in the dermis, clinically characterized by the development of pruritic, often pigmented, hyperkeratotic papules on trunk and extremities, especially on the shins, and histologically by the deposition of amyloid or amyloid-like proteins in the papillary dermis.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Lichen amyloidosis | Amyloid lichen · Lichen amyloidosus |
| fr | Lichen amyloïde | Amylose cutanée papuleuse |
| de | Lichen amyloidosus | |
| es | Amiloidosis liquenoide | Liquen amiloide |
| it | Lichen - amiloidosi | Lichen amiloide · Lichen amiloidosico |
| nl | Lichen amyloidosus | Amyloidosis cutis papulosa · Lichen amyloïdose · Papuleuze amyloïdose |
| pt | Líquen amiloidótico | |
| pl | Liszaj amyloidowy | Liszaj amyloidowy · Liszaj amyloidowy |
| cs | Lichen amyloidosus | Amyloidní lichen |
| uk | Лишайний амілоїдоз | Амілоїдний лишай · Амілоїдозний лишай |
| zh | 苔藓样淀粉样变病 | 苔藓样淀粉样变病 |
| tr | Liken amiloidoz | Amiloid liken · Liken amiloidozu |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | E85.4+ | NTBT | index | validated |
| ICD-10 | L99.0* | NTBT | inclusion | validated |
| ICD-11 | 5D00.0 | NTBT | index | validated |
| MONDO | 0018856 | E | validated | |
| UMLS | C5779561 | 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 (1):
- ORPHA:137807Primary cutaneous amyloidosis
rare skin diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
2 annotations · validated 2016-06-01| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0200034 | Papule | |
| HP:0000989 | Pruritus | |
Run the differential on the 2 obligate / very frequent terms
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/49804
- This record as JSON: /data/d/49804.json