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| LETTER TO EDITOR |
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| Year : 2017 | Volume
: 14
| Issue : 4 | Page : 240 |
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Ollier disease
Robert U Ashford
Department of Cancer Studies, University Hospitals of Leicester NHS Trust, Leicester Royal Infirmary, Leicester, LE1 5WW, United Kingdom
| Date of Web Publication | 5-Feb-2018 |
Correspondence Address:
Robert U Ashford
Department of Cancer Studies, University Hospitals of Leicester NHS Trust, Leicester Royal Infirmary, Leicester, LE1 5WW
United Kingdom
 Source of Support: None, Conflict of Interest: None
DOI: 10.4103/am.am_3_18
How to cite this article:
Ashford RU. Ollier disease. Apollo Med 2017;14:240 |
The article by Ali is entitled Ollier Disease (Apollo Medicine 2017; 14: 72-74).
The author then describes a case of a child with multiple exostoses, confirmed by the radiology.
Ollier disease is multiple enchondromata rather than multiple exostoses. It is likely the child had multiple hereditary exostoses (formerly known as diaphyseal aclasis) rather than Ollier disease.
It is important to recognize the difference between the two conditions.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
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