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Treatment of Ribbing disease with 5-year follow-up and literature review
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 m...
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Published in: | Osteoporosis international 2017-04, Vol.28 (4), p.1499-1502 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 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 5Â years. The radiological changes and the clinical effects are described, and the different Ribbing treatments are then briefly reviewed. |
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ISSN: | 0937-941X 1433-2965 |
DOI: | 10.1007/s00198-016-3896-9 |