Cavitary myiasis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Cavitary myiasis is a rare parasitic disease characterized by the infestation of natural body cavities (e.g. aural, nasal, oral, urogenital myiasis) and internal organs (e.g. cerebral myiasis, ophthalmomyiasis, intestinal and tracheopulmonary myiasis) with dipteran larvae. Clinical presentation is variable depending on the affected site(s) and degree of infestation and include foreign-body sensation (with or without movement sensation), hemorrhage, pain, edema, sensory loss, malodor, and pruritus, among others. Neurological features (e.g. motor deficits, seizures, reduced mental status, extrapyramidal signs) have been reported in cerebral myiasis.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Cavitary myiasis | |
| fr | Myiase des cavités | |
| de | Kavitarmyiasis | Körperhöhlen-Myiasis |
| es | Miasis cavitaria | |
| it | Miasi cavitaria | |
| nl | Cavitaire myiasis | |
| pt | Miíase cavitária | |
| pl | Muszyca jamy ciała | |
| cs | Kavitární myiáze | |
| uk | Кавернозний міаз | |
| zh | 空洞性蝇蛆病 | |
| tr | Kaviter miyazi |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B87.8 | NTBT | attributed | validated |
| ICD-11 | 1G01.0 | BTNT | specific | validated |
| ICD-11 | 1G01.1 | BTNT | specific | validated |
| ICD-11 | 1G01.2 | BTNT | specific | validated |
| ICD-11 | 1G01.Y | NTBT | index | validated |
| MONDO | 0015623 | E | validated | |
| UMLS | C4707154 | 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:75110Myiasis
rare infectious diseases - ORPHA:716348Rare isolated progressive predominantly chorioretinal disorder
rare ophthalmic disorders
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 | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 28822697[PMID]_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/165958
- This record as JSON: /data/d/165958.json