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LIPOMATOSIS OF SKELETAL MUSCLE IN MAFFUCCI'S SYNDROME

A. H. Cameron 1; and D. H. McMillan 1

1 The Department of Pathology, University of Sheffield, Department of Orthopaedics, Sheffield Royal Infirmary

A boy aged eleven with a solitary chondroma of the right tibia, and angiomata of the skeletal muscle, subcutaneous tissues, and periarticular tissues of the same limb, is considered to be a case of Maffucci's syndrome (dyschondroplasia with angiomata), although there was not the severe deformity encountered in the previously reported cases. There was a secondary atrophy and adiposity of skeletal muscle, and this was attributed to anoxic effects produced by the angiomata.
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Registered charity no: 209299     Print ISSN: 0301-620X
Hip, Knee, Trauma, Upper limb, Foot & Ankle, Paediatrics, Oncology, Spine, Arthroplasty, General