Orimolade E A, Ikem I C, Oginni L M, Odunsi A O
Department of Orthopaedic Surgery and Traumatology, Obafemi Awolowo University Teaching Hospital, Ile-Ife, Nigeria.
Niger J Clin Pract. 2011 Oct-Dec;14(4):492-4. doi: 10.4103/1119-3077.91764.
Femoral bifurcation and tibia hemimelia are rare anomalies. Hereby, we present a case report of a 2-year-old boy who first presented in our orthopedic clinic as a 12-day-old neonate, with a grossly deformed right lower limb from a combination of complete tibia hemimelia and ipsilateral femoral bifurcation. Excision of femoral exostosis, knee disarticulation and prosthetic fitting gives satisfactory early outcome.
股动脉分叉和胫骨半侧发育不全是罕见的畸形。在此,我们报告一例2岁男孩的病例,该男孩12天大时首次到我们的骨科门诊就诊,因合并完全性胫骨半侧发育不全和同侧股动脉分叉导致右下肢严重畸形。切除股骨外生骨疣、膝关节离断术和假肢安装取得了满意的早期效果。