raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:228243

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enElastofibroma dorsi
frElastofibromeElastofibrome dorsal
deElastofibroma dorsi
esElastofibroma dorsal
itElastofibroma dorsale
nlElastofibroma dorsi
ptElastofibroma dorsal
plWłókniak sprężysty grzbietu
csElastofibroma dorsi
ukЕластофіброма спини
zh背部弹力蛋白纤维瘤
trElastofibroma dorsi

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10L98.8NTBTattributedvalidated
ICD-11EE6YNTBTattributedvalidated
MONDO0016440Evalidated
UMLSC0346042Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card