Maffucci syndrome

Maffucci syndrome is a rare, non-inherited abnormality characterised by multiple enchondromas, bone deformity and vascular (occasionally lymphatic) malformations. The genetic defect is unknown. Ollier’s disease is a related condition in which there are multiple enchondromas, but no vascular malformations.

Enchondromas classically occur in the long bones and in the hands and feet, although involvement of the skull, ribs and vertebrae are described. The vascular malformations often appear as soft tissue masses with a bluish tinge in the skin, and are often partially calcified on x-ray.

The diagnosis is made clinically as there is no specific laboratory test, and patients may come to diagnosis at any age, depending on the severity of the condition.

The risk of malignancy is higher than in Ollier’s disease: the major concern is around the degeneration of enchondromas to central chondrosarcomas, but there can be associated malignancies including brain tumours and it is these which are possibly more likely to be life threatening. As with other rare syndromes estimating the absolute risk of malignancy is difficult: one study of seven patients reported that malignant change was a “certainty”, but this was a small study likely subject to referral bias. There appears to be a consensus that life expectancy is relatively normal.

Treatment tends to be symptomatic: large enchondromas may need curettage, particularly where hand function is impaired. Patients are followed for changes in symptoms or in the size of their enchondromas.

For an overview of enchondromatosis syndromes look at Pansuriya’s article.

The Orphanet entry for Maffucci syndrome can be found here.

3 thoughts on “Maffucci syndrome

  1. I’m getting a bit confused with all these multiple enchondroma type conditions.

    Am I correct in thinking that Olliers and Maffucci are non hereditary and hereditary multiple exostoses is well… hereditary.

    • Spot on – Olliers disease and Maffucci syndrome are sporadic – familial cases are very rare indeed. Multiple osteochondromatosis (aka hereditary multiple exostoses) is an autosomal dominant and is the most common skeletal dysplasia. Does that help?

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