Bullous impetigo
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A rare, acquired, typically benign, bacterial infectious disease caused by <i>Staphylococcus aureus</i> characterized by large, fragile vesicles and flaccid bullae on an erythematous base, which evolve into moistened erosions with a thin, varnish-like crust, usually localized in intertriginous areas of the trunk and extremities (armpits, groins, between the fingers or toes, beneath the breasts). Although uncommon, systemic symptoms, such as fever, diarrhea, and weakness, may be associated.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Bullous impetigo | |
| fr | Impétigo bulleux | |
| de | Impetigo, bullöse | |
| es | Impétigo ampolloso | Impétigo bulloso |
| it | Impetigine bollosa | |
| nl | Bulleuze impetigo | |
| pt | Impetigo bolhoso | |
| pl | Liszajec pęcherzowy | |
| cs | Bulózní impetigo | |
| uk | Бульозний імпетиго | |
| zh | 大疱性脓疱疮 | |
| tr | Büllöz impetigo |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | L01.0 | NTBT | attributed | validated |
| ICD-11 | 1B72.0 | E | specific | validated |
| MONDO | 0018182 | E | validated | |
| UMLS | C1542647 | E | validated | |
| MedDRA | 10006563 | 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:90077Other acquired skin disease
rare skin diseases - ORPHA:300579Staphylococcal toxemia
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
8 annotations · validated 2016-06-01| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0008066 | Abnormal blistering of the skin | |
| HP:0010783 | Erythema | |
| HP:0200039 | Pustule | |
| HP:0005406 | Recurrent bacterial skin infections | |
| Occasional (29-5%) | ||
| HP:0100763 | Abnormality of the lymphatic system | |
| HP:0100820 | Glomerulopathy | |
| HP:0100806 | Sepsis | |
| HP:0003095 | Septic arthritis | |
Run the differential on the 4 obligate / very frequent terms
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/36237
- This record as JSON: /data/d/36237.json