Solitary bone cyst
Synonyms: Juvenile bone cyst
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Childhood
- Status
- active
A benign non-epithelial bone cavity that is asymptomatic and that is found most commonly in the second decade of life by chance. The long bones are most often affected, but cases involving the jaw bone have been reported.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Solitary bone cyst | Juvenile bone cyst |
| fr | Kyste osseux solitaire | Kyste osseux juvénile |
| de | Knochenzyste, solitäre | Knochenzyste, juvenile |
| es | Quiste óseo solitario | Quiste óseo juvenil |
| it | Cisti ossea solitaria | Cisti ossea giovanile |
| nl | Solitaire botcyste | Juveniele botcyste |
| pt | Quisto ósseo solitário | Quisto ósseo juvenil |
| pl | Pojedyńcza torbiel kości | Pojedyńcza torbiel kostna |
| cs | Solitární kostní cysta | Jednokomorová kostní cysta |
| uk | Солітарна кісткова кіста | Однокамерна кістома кістки |
| zh | 单一性骨囊肿 | 单房性骨囊肿 |
| tr | Soliter kemik kisti | Tek kamaralı kemik kisti |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | M85.4 | E | specific | validated |
| ICD-11 | FB80.5 | E | specific | validated |
| MONDO | 0019372 | E | validated | |
| UMLS | C0005937 | 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:68411Rare bone tumor
rare bone diseases; rare neoplastic 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
17 annotations · validated 2019-06-06| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0012064 | Unicameral bone cyst | |
| Frequent (79-30%) | ||
| HP:0003926 | Abnormality of the humeral diaphysis | |
| HP:0100253 | Abnormality of the medullary cavity of the long bones | |
| HP:0002653 | Bone pain | |
| HP:0002756 | Pathologic fracture | |
| HP:0006431 | Proximal femoral metaphyseal abnormality | |
| Occasional (29-5%) | ||
| HP:0002992 | Abnormality of tibia morphology | |
| HP:0012428 | Prominent calcaneus | |
| Very rare (<4-1%) | ||
| HP:0003312 | Abnormal form of the vertebral bodies | |
| HP:0002696 | Abnormal parietal bone morphology | |
| HP:0002867 | Abnormality of the ilium | |
| HP:0000707 | Abnormality of the nervous system | |
| HP:0003172 | Abnormality of the pubic bone | |
| HP:0002143 | Abnormality of the spinal cord | |
| HP:0003418 | Back pain | |
| HP:0003979 | Lytic defects of the radius | |
| HP:0100748 | Muscular edema | |
Run the differential on the 1 obligate / very frequent terms
Annotation source: 27075249[PMID]_27554346[PMID]_30691312[PMID]_30726590[PMID]_30969659[PMID]_30969671[PMID]
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/83468
- This record as JSON: /data/d/83468.json