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PubMed · 15756363

Jaffe-Campanacci syndrome.

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

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Bone NeoplasmsCafe-au-Lait SpotsChildDiagnosis, DifferentialFibromaHumansMaleNeurofibromatosesSyndromeCase ReportsJournal Article

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BibTeXRIS

Ammar C Al-Rikabi, Jyothi C Ramaswamy, Venkatraman V Bhat. 2005. Jaffe-Campanacci syndrome.. https://pubmed.ncbi.nlm.nih.gov/15756363/

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