A Case of Sporadic Caffey's Disease(Infantil Cortical Hyperostosis) Without Mandibular Involvement
Journal of the Korean Pediatric Society
;
: 1294-1299, 2000.
Article
Dans Coréen
| WPRIM
| ID: wpr-208773
ABSTRACT
Caffey's disease(infantile cortical hyperostosis) is an uncommon benign and self limited disorder of unknown etiology, affecting the skeleton and its contiguous fasciae and muscles. Its occurrence in isolated cases or in multiple members in families suggests the existence of two different forms, namely a sporadic form and a familial form. The tibia is the predominant bone known to be affected in the familial form, while the mandible is mostly affected in the sporadic form. This benign and self-limited disorder has rarely late recurrence or persistence of symptoms with deformity. The patient in this case had immediate and complete resolution of her symptoms while receiving acetaminophen with no recurrent bone formation during treatment with antiinflammatory drugs. We describe sporadic, nonfamilial Caffey's disease, affecting both radii and tibiae, but not involving the mandibular in a 4-month-old female infant.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Ostéogenèse
/
Récidive
/
Squelette
/
Malformations
/
Tibia
/
Hyperostose corticale infantile
/
Fascia
/
Mandibule
/
Acétaminophène
/
Muscles
Limites du sujet:
Femelle
/
Humains
/
Bébé
langue:
Coréen
Texte intégral:
Journal of the Korean Pediatric Society
Année:
2000
Type:
Article
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