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Updated: May 11, 2026

Culture of Murine Embryonic Metatarsals: A Physiological Model of Endochondral Ossification
Published on: December 3, 2016
An unusual complication in a 9-year-old patient with hereditary multiple osteochondromatosis
Carlos E Calvo1, Maricarmen Cruz, Edwardo Ramos
1VA Caribbean Healthcare System, Physical Medicine and Rehabilitation, 10 Casia St, San Juan, PR. cec338@yahoo.com
Abstract:
This case report describes the presentation of a 9-year-old boy with a history of hereditary multiple osteochondromatosis who presented to the outpatient setting with progressive difficulty in ambulation. Magnetic resonance imaging of the spine revealed a thoracic spinal tumor, which was surgically removed. After surgery, the boy's ambulation and spasticity/contractures improved. This case is unique because this complication of hereditary multiple osteochondromatosis was identified at an age and in a region that are not typical. From a clinical standpoint, early identification of this complication is important because surgical treatment typically leads to good outcomes.
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