The neoplastic pathogenesis of solitary and multiple osteochondromas

DE Porter, A Simpson - The Journal of pathology, 1999 - Wiley Online Library
DE Porter, A Simpson
The Journal of pathology, 1999Wiley Online Library
Many theories of osteochondroma pathogenesis have been advanced. Genetic research
into the inherited multiple form, hereditary multiple exostoses, has revealed a new family of
tumour suppressor genes denoted EXT. Patterns of EXT gene mutation in hereditary
multiple exostoses, in solitary and multiple osteochondromas, and in chondrosarcoma are
analogous to those found in other tumour suppressor genes responsible for family cancer
traits and associated malignancies. With one exception, most features of osteochondroma …
Abstract
Many theories of osteochondroma pathogenesis have been advanced. Genetic research into the inherited multiple form, hereditary multiple exostoses, has revealed a new family of tumour suppressor genes denoted EXT. Patterns of EXT gene mutation in hereditary multiple exostoses, in solitary and multiple osteochondromas, and in chondrosarcoma are analogous to those found in other tumour suppressor genes responsible for family cancer traits and associated malignancies. With one exception, most features of osteochondroma behaviour are comparable to those of benign neoplasms. The neoplastic pathogenesis of osteochondromas provides an alternative to the traditional ‘skeletal dysplasia’ theory to explain the growth disturbance associated with hereditary multiple exostoses. Recent studies on the physiological function of EXT genes are reviewed and implications for osteochondroma ‘cell‐of‐origin’ theories are discussed. Copyright © 1999 John Wiley & Sons, Ltd.
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