Sonar Mehmet, Isik Mustafa, Ekmekci Aslihan Yilmaz, Solmaz Ozgen Arslan
Department of Orthopaedics, Elazig Training and research Hospital, Elazig, Turkey.
BMJ Case Rep. 2012 Oct 19;2012:bcr2012007047. doi: 10.1136/bcr-2012-007047.
Jaffe-Campanacci's syndrome is a very rare condition and was first described by Jaffe in 1958. It is presented by non-ossifying fibromas, café-au-lait spots and axillar freckling. Non-ossifying fibromas are usually found after minor traumas or stress fractures. Differential diagnosis to neurofibromatosis include the absence of Lisch granules, neurofibromatous skin lesions and schwannomatous soft tissue masses. In this case, we report a 13-year-old white boy with Jaffe-Campanacci's syndrome, and bilateral pathological lower limbs fracture.
贾菲-坎帕纳奇综合征是一种非常罕见的病症，于1958年由贾菲首次描述。它表现为非骨化性纤维瘤、咖啡斑和腋窝雀斑。非骨化性纤维瘤通常在轻微创伤或应力性骨折后被发现。与神经纤维瘤病的鉴别诊断包括无Lisch结节、神经纤维瘤性皮肤病变和神经鞘瘤性软组织肿块。在此病例中，我们报告了一名患有贾菲-坎帕纳奇综合征的13岁白人男孩，其双侧下肢发生病理性骨折。
