SciELO - Scientific Electronic Library Online

 
vol.41 issue3Linear Epidermal Nevus with Epidermolytic Hyperkeratosis Case description author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

  • Have no cited articlesCited by SciELO

Related links

  • Have no similar articlesSimilars in SciELO

Share


Pediatría (Asunción)

On-line version ISSN 1683-9803

Abstract

GRAU, Lorena et al. Sclerosing Osteomyelitis of Garre: Report of a Case in a Pediatrics Department. Pediatr. (Asunción) [online]. 2014, vol.41, n.3, pp.219-222. ISSN 1683-9803.

Introduction: Chronic sclerosing osteomyelitis of Garre (GSO) is a rare entity that affects children and young adults. The GSO process is characterized by a marked osteoblastic response, generally appearing in the long bones or mandible, with the original description being of a case in the mandible. Case Report: A male patient aged 14 years with a one-week history of swelling of the face with inflammatory signs and spontaneous drainage of purulent liquid.  He was initially treated with antibiotics due to the presence of an area of cellulitis. Drainage of the abscess and tooth extraction were also performed. No microorganism was isolated. In view of poor response to antibiotic therapy a bone scan was done that found increased uptake in the mandibullar ramus, with GSO later confirmed by bone biopsy. Discussion: Few clinical cases of Garre’s sclerosing osteomyelitis have been reported. Most agree that GSO affects children and young adults. The most common locations are the metaphyseal portions of the long bones and the jaw. The cause is unknown, but microscopic findings suggest a possible infectious origin.

Keywords : Sclerosing osteomyelitis; Garre’s; children.

        · abstract in Spanish     · text in Spanish     · Spanish ( pdf )

 

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License