Myospherulosis
Synonyms: Spherulocytosis · Subcutaneous spherulocystic disease
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
A rare maxillo-facial surgical disease characterized by an inflammatory, granulomatous lesion, most commonly of iatrogenic origin due to interaction of extravasated erythrocytes with exogenous lipids, in particular petrolatum-based antibiotic ointment used after surgical procedures. Most frequent locations are the paranasal sinuses and jaws, although the lesion can occur in any part of the body. It is typically found incidentally as an asymptomatic soft tissue swelling.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Myospherulosis | Spherulocytosis · Subcutaneous spherulocystic disease |
| fr | Myosphérulose | Sphérulocytose |
| de | Myospherulose | Spherulozytose |
| es | Mioesferulosis | Enfermedad esferuloquística subcutánea · Esferulocitosis |
| it | Miosferulosi | Sferulocitosi |
| nl | Myosferulose | Sferulocytose · Subcutane sferulocystische ziekte |
| pt | Miosferulose | |
| pl | Sferulozytoza mięśniowa | Sferulozytoza |
| cs | Myosferulóza | Sferulocytóza |
| uk | Міосферульоз | Сфероцитоз · Підшкірна сферолоцитарна хвороба |
| zh | 肌小球体病 | 皮下球样囊肿 |
| tr | Miyosferüloz | Sferositoz · Deri altı sferülokistik hastalık |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | T88.8 | NTBT | attributed | validated |
| MONDO | 0017628 | E | validated | |
| UMLS | C0027123 | 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:165711Rare abdominal surgical disease
rare abdominal surgical diseases - ORPHA:68329Rare maxillo-facial surgical disease
rare surgical maxillo-facial 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/306553
- This record as JSON: /data/d/306553.json