Kerion celsi
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A rare inflammatory and suppurating type of tinea capitis, a skin infection caused by <i>Trichophyton</i> or <i>Microsporum</i> fungi, that predominantly affects the scalp and that is characterized by the development of painful crusty lesions covered with follicular pustules and surrounded by erythematous alopecic areas, that can later evolve into abscesses and leave permanent cicatricial alopecia. Lesions can be associated with regional lymphadenopathy.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Kerion celsi | |
| fr | Kérion de Celse | |
| de | Kerion Celsi | |
| es | Querión de Celso | |
| it | Kerion celsi | |
| nl | Kerion celsi | Tinea kerion |
| pt | Kerion celsi | |
| pl | Grzybica owłosionej skóry głowy ze stanem zapalnym | |
| cs | Kerion celsi | |
| uk | Керіон (Kerion celsi) | |
| zh | 塞耳斯脓癣 | |
| tr | Kerion celsi |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B35.0 | NTBT | index | validated |
| ICD-11 | 1F28.4 | E | specific | validated |
| MONDO | 0010146 | E | validated | |
| UMLS | C0276742 | E | validated | |
| GARD | 3109 | 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:90077Other acquired skin disease
rare skin diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
8 annotations · validated 2016-06-01| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0011123 | Inflammatory abnormality of the skin | |
| HP:0100838 | Recurrent cutaneous abscess formation | |
| HP:0001581 | Recurrent skin infections | |
| Frequent (79-30%) | ||
| HP:0001596 | Alopecia | |
| HP:0001945 | Fever | |
| HP:0002716 | Lymphadenopathy | |
| Occasional (29-5%) | ||
| HP:0002076 | Migraine | |
| HP:0003326 | Myalgia | |
Run the differential on the 3 obligate / very frequent terms
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/499
- This record as JSON: /data/d/499.json