Deep dermatophytosis
Synonyms: Disseminated granulomatous dermatophytosis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult, Childhood
- Status
- active
A rare mycosis characterized by severe, potentially life-threatening dermal and subcutaneous tissue invasion by dermatophytes. Dissemination to lymph nodes is frequent, but the infection may also occasionally spread to the central nervous system. Cutaneous signs and symptoms include erythema, desquamation, itching, nodules, plaques, or ulceration. The majority of deep dermatophytoses develop in immunocompromised patients.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Deep dermatophytosis | Disseminated granulomatous dermatophytosis |
| fr | Dermatophytose profonde | Dermatophytie granulomateuse à foyers disséminés · Maladie dermatophytique |
| de | Tiefe Dermatophytose | Disseminierte granulomatöse Dermatophytose |
| es | Dermatofitosis profunda | Dermatofitosis granulomatosa diseminada |
| it | Dermatofitosi profonda | Dermatofitosi granulomatosa disseminata |
| nl | Diepe dermatofytose | Verspreide granulomateuze dermatofytose |
| pt | Dermatofitose profunda | |
| pl | Dermatofitoza głęboka | Rozsiana dermatofitoza ziarniniakowata |
| cs | Hluboká dermatofytóza | Diseminovaná granulomatózní dermatofytóza |
| uk | Глибокий дерматофітоз | Дисемінована гранульоматозна дерматофітія |
| zh | 深部皮肤癣菌病 | 播散肉芽肿性皮肤霉菌病 |
| tr | Derin dermatofitoz | Yaygın granülomatöz dermatofitoz |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B35.8 | NTBT | inclusion | validated |
| ICD-11 | 1F28.Y | NTBT | attributed | validated |
| MONDO | 0021660 | E | validated | |
| UMLS | C1395264 | 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:163591Rare mycosis
rare infectious 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
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/397587
- This record as JSON: /data/d/397587.json