Elastofibroma dorsi
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
Elastofibroma dorsi is a rare, acquired, dermis elastic tissue disorder characterized by a benign, slowly progressive, often bilateral, non-encapsulated lesion, usually presenting as an ill-defined mass under the inferior angle of the scapula (but other locations have been reported), which adheres to the deep layers and presents no local signs of inflammation. It is commonly asymptomatic and discovered inadvertently, but symptoms may include pain and discomfort or stiffness when using the shoulder. The presence of a firm mass masked by the scapula during retropulsion of the shoulder and becoming prominent when the shoulder is displaced toward the front is a frequent sign. Neuromuscular involvement of the upper limb may occur in rare cases.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Elastofibroma dorsi | |
| fr | Elastofibrome | Elastofibrome dorsal |
| de | Elastofibroma dorsi | |
| es | Elastofibroma dorsal | |
| it | Elastofibroma dorsale | |
| nl | Elastofibroma dorsi | |
| pt | Elastofibroma dorsal | |
| pl | Włókniak sprężysty grzbietu | |
| cs | Elastofibroma dorsi | |
| uk | Еластофіброма спини | |
| zh | 背部弹力蛋白纤维瘤 | |
| tr | Elastofibroma dorsi |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | L98.8 | NTBT | attributed | validated |
| ICD-11 | EE6Y | NTBT | attributed | validated |
| MONDO | 0016440 | E | validated | |
| UMLS | C0346042 | 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):
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/228243
- This record as JSON: /data/d/228243.json