Jaffe-Campanacci syndrome.

Authors

• Ammar C. Al-Rikabi
• Jyothi C. Ramaswamy
• Venkatraman V. Bhat

Abstract

This case report describes the clinical, radiological and histopathological features of the Jaffe-Campanacci syndrome as seen in a 6-year-old Qatari male patient who was initially misdiagnosed as a case of systemic neurofibromatosis. Our case has all the diagnostic stigmata of Jaffe-Campanacci syndrome as described in the literature and these include cafe au lait macules, skeletal deformities and multiple histologically confirmed non-ossifying fibromas of the long bones.

Article Type

Case Report

First Page

104

Last Page

106

Recommended Citation

Al-Rikabi, Ammar C.; Ramaswamy, Jyothi C.; and Bhat, Venkatraman V. (2005) "Jaffe-Campanacci syndrome.," Saudi Medical Journal: Vol. 26: Iss. 1, Article 19.
DOI: https://doi.org/10.15537/1658-3175.2792