多发性遗传性骨软骨瘤病中的髋关节半脱位：两例报告。
Subluxation of the hip joint in multiple hereditary osteochondromatosis: report of two cases.
作者信息
Woodward M N, Daly K E, Dodds R D, Fixsen J A
机构信息
Great Ormond Street Hospital for Sick Children, London, England.
出版信息
J Pediatr Orthop. 1999 Jan-Feb;19(1):119-21.
PMID:9890300
Abstract
We report two cases of children with multiple hereditary osteochondromatosis (MHO) in whom painful restriction of hip movement developed due to intraacetabular osteochondromata. Excision of the lesions relieved pain and restored joint movement after 14 and 3 months' follow-up, respectively. Long-term follow-up of these patients is essential.
摘要
我们报告两例患有多发性遗传性骨软骨瘤病（MHO）的儿童，他们因髋臼内骨软骨瘤而出现髋关节活动受限伴疼痛。分别在14个月和3个月的随访后，切除病灶缓解了疼痛并恢复了关节活动。对这些患者进行长期随访至关重要。
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