ORPHA:141067

Cervicofacial fibrochondroma

Type: Morphological anomaly
Group: Disorder
Status: active

A rare extraskeletal chondroma located in the head and neck region, histologically typically characterized by lobules of mature, adult hyaline cartilage with chondrocytic cells identifiable in lacunae, and prominent fibrosis. Malignant transformation has not been described.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Cervicofacial fibrochondroma
fr	Fibrochondrome cervico-facial
de	Fibrochondrom, zervikofaziales
es	Fibrocondroma cervicofacial
it	Fibrocondroma cervico-facciale
nl	Cervicofaciaal fibrochondroom
pt	Fibrocondroma cervicofacial
pl	Włókniakochrzęstniak szyi i twarzy	Chrzęstniak śródkostny szyjno-twarzowy
cs	Cervikofaciální fibrochondrom	Cervikofaciální enchondrom
uk	Шийно-лицьова фіброхондрома
zh	颈面部纤维软骨瘤
tr	Servikofasiyal fibrokondrom

Definition in:

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-10	D21.0	NTBT	attributed	validated
ICD-11	LA6Y	NTBT	index	validated
MONDO	0015383	E		validated
UMLS	C5231314	E		validated
GARD	19941	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):

ORPHA:68329Rare maxillo-facial surgical disease

Parents in the classifications (1):

ORPHA:155835Cysts and fistulae of the face and oral cavity
rare developmental anomalies during embryogenesis; rare otorhinolaryngological diseases

No children.

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No 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/141067
This record as JSON: /data/d/141067.json