J Korean Pediatr Soc.  2000 Sep;43(9):1294-1299.

A Case of Sporadic Caffey's Disease(Infantil Cortical Hyperostosis) Without Mandibular Involvement

Affiliations
  • 1Department of Pediatrics, Presbyterian Medical Center, Chonju, Korea.

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.

Keyword

Caffey's disease; Infantile cortical hyperostosis; Sporadic; Familial

MeSH Terms

Acetaminophen
Congenital Abnormalities
Fascia
Female
Humans
Hyperostosis, Cortical, Congenital
Infant
Mandible
Muscles
Osteogenesis
Recurrence
Skeleton
Tibia
Acetaminophen
Full Text Links
  • KJP
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr