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Review
. 1989 Mar-Apr;28(2):162-5.

Osteochondromatosis (diaphyseal aclasis): a case report and literature review

Affiliations
  • PMID: 2661639
Review

Osteochondromatosis (diaphyseal aclasis): a case report and literature review

M D Perlman et al. J Foot Surg. 1989 Mar-Apr.

Abstract

An unusual case of osteochondromatosis is presented with a review of the literature. Osteochondromatosis, also known as hereditary multiple exostoses or diaphyseal aclasis, are inherited, benign, cartilaginous neoplasms that consist of a pedicle of normal bone covered with proliferating cartilage cells. Pathologic, clinical, and radiographic findings will be discussed.

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