Treatment of Ribbing disease with 5-year follow-up and literature review.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 28101629.
- Also identified by DOI 10.1007/s00198-016-3896-9.
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Abstract
Ribbing disease, or multiple diaphyseal sclerosis, is a rare diaphyseal sclerosis of unknown etiology. Patients with this pathology usually present with asymmetric pain limited to the lower extremities. Though all efforts are made to relieve the progressive pain associated with Ribbing disease, no medical or surgical treatments have been established yet. In this case report, we followed up a Ribbing case with sclerotic bone fenestration for 5 years. The radiological changes and the clinical effects are described, and the different Ribbing treatments are then briefly reviewed.
Medical subject headings
- Camurati-Engelmann Syndrome
- Osteoma, Osteoid