Osteogenesis imperfecta and hyperplastic callus formation in a family:: a report of three cases and a review of the literature

被引:16
作者
Ramírez, N
Vilella, FE
Colón, M
Flynn, JM
机构
[1] Mayaguez Med Ctr, Dept Orthopaed, Mayaguez, PR USA
[2] Univ Puerto Rico, Sch Med, Dept Orthopaed, San Juan, PR 00936 USA
[3] Vet Adm Hosp, Orthopaed Sect, San Juan, PR USA
来源
JOURNAL OF PEDIATRIC ORTHOPAEDICS-PART B | 2003年 / 12卷 / 02期
关键词
osteogenesis imperfecta; hyperplastic callus;
D O I
10.1097/01202412-200303000-00002
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Osteogenesis imperfecta is one of the most common groups of inherited disorders of connective tissue. Hyperplastic callus formation in patients with osteogenesis imperfecta after fracture or surgery is a rare occurrence that has often been misdiagnosed as osteosarcoma. Previous series reported that hyperplastic callus formation is more often present in osteogenesis imperfecta male patients, with white sclerae, and a negative family history of the disorder. This is the first time that this complication has been presented in three female siblings, with a positive family history of osteogenesis imperfecta type IV. An association between osteogenesis imperfecta type IV and hyperplastic callus formation is unclear. This association might, however, be a separate, specific subtype of osteogenesis imperfecta, with an unknown inheritance pattern. (C) 2003 Lippincott Williams Wilkins.
引用
收藏
页码:88 / 96
页数:9
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