A new syndrome mimicking Jaffe-Campanacci syndrome: a case report


SEVENCAN A., İNAN U., KÖSE N.

EKLEM HASTALIKLARI VE CERRAHISI-JOINT DISEASES AND RELATED SURGERY, vol.24, no.1, pp.46-48, 2013 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 24 Issue: 1
  • Publication Date: 2013
  • Doi Number: 10.5606/ehc.2013.11
  • Journal Name: EKLEM HASTALIKLARI VE CERRAHISI-JOINT DISEASES AND RELATED SURGERY
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
  • Page Numbers: pp.46-48
  • Keywords: Abnormality, cafe-au-lait spots, Jaffe-Campanacci syndrome, neurofibromatosis, non-ossifying fibroma, simple bone cyst, skeleton
  • Eskisehir Osmangazi University Affiliated: Yes

Abstract

Jaffe-Campanacci syndrome (JCS) is a well-known condition with its clinical and radiological characteristics. Extraskeletal congenital anomalies of this syndrome include cafe-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.