Aneurysmal bone cyst
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
A rare bone tumor characterized by a benign, cystic lesion consisting of blood-filled cavities divided by fibrous septa containing fibroblasts, multinucleated osteoclast-type giant cells, and reactive woven bone. The tumor may arise <i>de novo</i> or secondarily, complicating other benign or malignant bone tumors. It most commonly arises during the first two decades of life and often affects the epiphyses of long bones and posterior elements of vertebral bodies. Patients typically present with pain and swelling, or neurological symptoms due to compression of nerve roots or the spinal cord by vertebral tumors.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Aneurysmal bone cyst | |
| fr | Kyste osseux anévrysmal | KOA · Kyste anévrysmal de l'os |
| de | Aneurysmatische Knochenzyste | |
| es | Quiste óseo aneurismático | |
| it | Cisti ossea aneurismatica | |
| nl | Aneurysmatische botcyste | ABC |
| pt | Quisto ósseo aneurismático | |
| pl | Torbiel tętniakowata kości | |
| cs | Aneuryzmatická kostní cysta | |
| uk | Аневризмальна кісткова кіста | |
| zh | 动脉瘤性骨囊肿 | |
| tr | Anevrizmal kemik kisti |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | M85.5 | E | specific | validated |
| ICD-11 | FB80.6 | E | specific | validated |
| ICD-11 | XH23E0 | E | specific | validated |
| MONDO | 0018815 | E | validated | |
| MeSH | D017824 | E | validated | |
| UMLS | C0152244 | E | validated | |
| MedDRA | 10002362 | 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
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/480553
- This record as JSON: /data/d/480553.json