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A new syndrome mimicking Jaffe-Campanacci syndrome: a case report
Adnan Sevencan1, Ulukan İnan, Nusret Köse
1Department of Orthopedics and Traumatology, Medical Faculty of Eskişehir Osmangazi University, 26480 Meşelik, Eskişehir, Turkey. adnansevencan@hotmail.com
Abstract:
Jaffe-Campanacci syndrome (JCS) is a well-known condition with its clinical and radiological characteristics. Extraskeletal congenital anomalies of this syndrome include café-au-lait spots, mental retardation, cardiovascular abnormalities, ocular deformities, hypogonadism or cryptorchidism. Multiple non-ossifying fibromas are also characteristic bone lesions. In this article, we present a new syndrome mimicking JCS, which is characterized by a simple bone cyst and extraskeletal lesions.
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