Hisaoka M, Aoki T, Kouho H, Chosa H, Hashimoto H
Department of Pathology and Oncology, School of Medicine, University of Occupational and Environmental Health, Yahatanishi-ku, Kitakyushu, Japan.
Skeletal Radiol. 1997 Mar;26(3):191-4. doi: 10.1007/s002560050219.
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.
