{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,8,28]],"date-time":"2025-08-28T12:34:56Z","timestamp":1756384496945,"version":"3.40.4"},"reference-count":16,"publisher":"BMJ","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["BMJ Case Reports"],"abstract":"<jats:p>Jaffe-Campanacci's syndrome is a very rare condition and was first described by Jaffe in 1958. It is presented by non-ossifying fibromas, caf\u00e9-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.<\/jats:p>","DOI":"10.1136\/bcr-2012-007047","type":"journal-article","created":{"date-parts":[[2012,10,19]],"date-time":"2012-10-19T22:57:43Z","timestamp":1350687463000},"page":"bcr2012007047","source":"Crossref","is-referenced-by-count":4,"title":["Pathological fractures on both lower limbs with Jaffe-Campanacci's syndrome"],"prefix":"10.1136","volume":"2012","author":[{"given":"Mehmet","family":"Sonar","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mustafa","family":"Isik","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Aslihan Yilmaz","family":"Ekmekci","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ozgen Arslan","family":"Solmaz","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[2012,10,19]]},"reference":[{"key":"2025042707225358000_2012.oct19_1.bcr2012007047.1","unstructured":"Jaffe HL . Tumors and tumorous conditions of the bones and joints. Philadelphia: Lea and Febiger,1958:242\u201354. Neurofibromatosis."},{"key":"2025042707225358000_2012.oct19_1.bcr2012007047.2","first-page":"104","article-title":"Jaffe-Campanacci syndrome","volume":"26","author":"Al-Rikabi","year":"2005","journal-title":"Saudi Med J"},{"key":"2025042707225358000_2012.oct19_1.bcr2012007047.3","first-page":"1","article-title":"Non-ossifying fibroma, fibrous cortical defect and Jaffe-Campanacci syndrome: a biologic and clinical review","volume":"93","author":"Mankin","year":"2009","journal-title":"Chir Organi Mov"},{"key":"2025042707225358000_2012.oct19_1.bcr2012007047.4","doi-asserted-by":"publisher","DOI":"10.1007\/BF00350960"},{"key":"2025042707225358000_2012.oct19_1.bcr2012007047.5","doi-asserted-by":"crossref","first-page":"634","DOI":"10.2106\/00004623-200204000-00022","article-title":"Jaffe\u2013Campanacci syndrome. 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Bone and soft tissue tumors: clinical features, imaging, pathology and treatment. 2nd edn. 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