The case of a 49-year-old man with Maffucci’s syndrome, who developed multiple spindle cell hemangioendotheliomas, is presented. The case provides support for recent reports suggesting an association between this peculiar vascular lesion and skeletal enchondromatosis.
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Stanford Univ, Dept Dermatol, Div Pediat Dermatol, Sch Med, Stanford, CA 94305 USA
Mahidol Univ, Ramathibodi Hosp, Div Ambulatory & Adolescent Med, Dept Pediat,Sect Dermatol,Fac Med, Bangkok, ThailandStanford Univ, Dept Dermatol, Div Pediat Dermatol, Sch Med, Stanford, CA 94305 USA
Lekwuttikarn, Ramrada
Chang, James
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Stanford Univ, Med Ctr, Div Plast & Reconstruct Surg, Stanford, CA 94305 USAStanford Univ, Dept Dermatol, Div Pediat Dermatol, Sch Med, Stanford, CA 94305 USA
Chang, James
Teng, Joyce M. C.
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Stanford Univ, Dept Dermatol, Div Pediat Dermatol, Sch Med, Stanford, CA 94305 USAStanford Univ, Dept Dermatol, Div Pediat Dermatol, Sch Med, Stanford, CA 94305 USA