Multifocal tuberculosis
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Status
- active
A rare tuberculosis characterized by two or more extra-pulmonary lesions caused by <i>M. tuberculosis</i> with or without pulmonar involvement, mostly occur in immunocompromised patients. It may affect any site including liver, lymph nodes, lungs, pleura, and the joints. Cutaneous and/or skeletal involvement are rarely reported. Cutenous forms include gummas, scrofuloderma, vasculitis and lupus tuberculosis. Skeletal involvement, that may affect one or more joints, can be dominated by the involvement of large joints that support greater weigh loads, such as the knees and hips and the spine. The symptoms are usually nonspecific, and the disease often presents with an indolent clinical course. Risk factors include human immunodeficiency viruses, immunosuppression due to diverse causes, smoking, malnutrition, diabetes, and stress.
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Multifocal tuberculosis | |
| fr | Tuberculose multifocale | |
| de | Multifokale Tuberkulose | |
| es | Tuberculosis multifocal | |
| it | Tubercolosi multifocale | |
| nl | Multifocale tuberculose | |
| pt | Tuberculose multifocal | |
| pl | Gruźlica wieloogniskowa | |
| cs | Multifokální tuberkulóza | |
| uk | Мультифокальний туберкульоз |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | A18.8 | NTBT | attributed | validated |
| ICD-11 | 1B12.Y | NTBT | attributed | validated |
| MONDO | 0957465 | E | validated | |
| UMLS | C5816701 | 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:3389Tuberculosis
rare infectious 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
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/645854
- This record as JSON: /data/d/645854.json