Asynchronous progressive diaphyseal dysplasia

Oxford University Press (OUP) - Tập 15 - Trang 450-453 - 2005
Toshinori Sakai1, Yoshito Matsui1, Shinsuke Katoh1, Kiminori Yukata1, Daisuke Hamada1, Yoichiro Takata1, Hiromichi Yokoi2, Natsuo Yasui1
1Department of Orthopedics, Institute of Health Biosciences, The University of Tokushima Graduate School, Tokushima, Japan
2Department of Orthopedics, National Kagawa Children's Hospital, Kagawa, Japan

Tóm tắt

We report the case of a 42-year-old Japanese woman with unusual diaphyseal dysplasia of bilateral femora. Radiographs showed thickening and sclerosis of the cortex with resultant enlargement of the diaphysis, unclear demarcation of the surface of the cortex, and no periosteal reaction. These changes were found on the left femur at the first presentation, and those on the right femur developed within several years. Although this patient partly presented characteristics of Ribbing disease and Camurati–Engelmann disease, the focal involvement of bilateral femora suggested an unknown pathogenesis.

Tài liệu tham khảo

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