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Title: Horner Syndrome due to a solitary osteochondroma of C7: a case report and review of the literature. Author: Zhao CQ, Jiang SD, Jiang LS, Dai LY. Journal: Spine (Phila Pa 1976); 2007 Jul 15; 32(16):E471-4. PubMed ID: 17632387. Abstract: STUDY DESIGN: Case report and review of the literature. OBJECTIVE: To report a 23-year-old woman with osteochondroma of the lower cervical spine who presented with Horner syndrome and to review the relevant literature. SUMMARY OF BACKGROUND DATA: Osteochondroma is the most common benign lesion of bone but rarely affects the spine. METHODS: Clinical history, routine radiographs, and computed tomography study of the patient were described. A review of the relevant literature was also done. RESULTS: The patient demonstrated a complete disappearance of clinical symptoms on the follow-up examination 60 days after surgery. No patients with Horner syndrome due to a solitary cervical osteochondroma have been previously reported in English-language medical literature. CONCLUSION: Vertebral involvement of osteochondroma is rare, especially with neurologic compromise. A young patient is presented with a symptomatic solitary osteochondroma of the seventh cervical vertebra who had Horner syndrome. This case report supports surgical intervention of symptomatic osteochondroma of the cervical spine.[Abstract] [Full Text] [Related] [New Search]