OSTEOFIBROUS DYSPLASIA OF THE ULNA

Author:

Kamineni S.1,Briggs T. W. R.1,Saifuddin A.2,Sandison A.3

Affiliation:

1. Department of Orthopaedic Surgery

2. Department of Radiology

3. Department of Pathology, The Royal National Orthopaedic Hospital NHS Trust, Brockley Hill, Stanmore, Middlesex HA7 4LP, UK.

Abstract

Osteofibrous dysplasia is a rare condition usually affecting the tibiae and fibulae of males in the first two decades of life. Involvement at the ulna has also been reported in some cases. We describe an extensive, rapidly progressive lesion of the ulna in a three-year-old girl. The progression of the disease accelerated after a local marginal removal, and required extensive resection of the ulna with reconstruction using a fibular autograft. The particular features of this case are the change in the aggressive nature of the condition, which has not been previously reported. We believe that this is only the second recorded case of histologically proven involvement of the ulna.

Publisher

British Editorial Society of Bone & Joint Surgery

Subject

Orthopedics and Sports Medicine,Surgery

Cited by 10 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Osteofibrous dysplasia of the 8th rib: a case report;Indian Journal of Thoracic and Cardiovascular Surgery;2024-08-02

2. Progress in Clinical Research of Osteofibrous Dysplasia;Advances in Clinical Medicine;2024

3. Osteofibrous dysplasia of the tibia;The Bone & Joint Journal;2022-02-01

4. Bone (Orthopedic Pathology);Oncological Surgical Pathology;2020

5. Does osteofibrous dysplasia progress to adamantinoma and how should they be treated?;The Bone & Joint Journal;2017-03

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