Ollier disease
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| Ollier disease | |
|---|---|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| ICD-10 | Q78.4 |
| ICD-9-CM | 756.4 |
| OMIM | 166000 |
| DiseasesDB | 9212 |
| eMedicine | radio/247 |
| Patient UK | Ollier disease |
| MeSH | D004687 |
Ollier disease is a rare nonhereditary sporadic disorder where intraosseous benign cartilaginous tumors (enchondroma) develop close to growth plate cartilage. Prevalence is estimated at around 1 in 100,000.[1]
Contents
Eponyms
The disorder is named after French surgeon Louis Léopold Ollier.[2]
Clinical features
Nominally, the disease consists of multiple enchondromas which usually develop in childhood. The growth of these endochondromas usually stops after skeletal maturation.[3] The affected extremity is shortened (asymmetric dwarfism) and sometimes bowed due to epiphyseal fusion anomalies. Persons with Ollier disease are prone to breaking bones and normally have swollen, aching limbs.
Diagnosis
On radiographs, streaks of low density are seen projecting through the diaphyses into the epiphyses of the long bones, due to ectopic cartilage deposits. With age, the cartilage may calcify in the typical "snowflake" pattern.
Treatment
The deformities are managed surgically to preserve the function of the limb.[4]
Epidemiology
One person in every 100,000 is affected. Ollier disease is not normally diagnosed until toddler years because it is not very visible.
Associated conditions
Ollier disease carries a high risk of skeletal, visceral and brain malignancy which occurs in approximately 25% of patients. Regular systemic screening is recommended.[5] Juvenile granulosa cell tumour has been associated with the disease.[6] The incidence of secondary chondrosarcoma in Ollier disease is not known, but may be as high as 25%, pelvis and shoulder girdle being the commonest locations.[4] A related disorder called Maffucci syndrome named after Angelo Maffucci is characterized by enchondromas associated with multiple hemangiomas which usually occur in the hands and feet. Maffucci syndrome carries a higher risk for cancer.
Additional images
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Morbus Ollier Finger Roentgen.png
X-ray showing calcified enchondromas localized in finger a 37-year-old patient affected with Ollier disease
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Morbus Ollier Humerus Roentgen.jpg
X-ray showing enchondromas localized in the humerus of a 37-year-old patient affected with Ollier disease
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Morbus Ollier Radius Roentgen.png
X-ray showing enchondromas localized in the lower part of the radius of a 37-year-old patient affected with Ollier disease
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Morbus Ollier Radius MRT T1.png
MRI showing enchondromas localized in the lower part of the radius of a 37-year-old patient affected with Ollier disease
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Morbus Ollier Radius MRT T2.png
MRI showing enchondromas localized in the lower part of the radius of a 37-year-old patient affected with Ollier disease.
See also
References
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- ↑ synd/1813 at Who Named It?
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