Coincidence of Congenital Pseudarthrosis of the Tibia and Hemihypertrophy in a Patient With Neurofibromatosis Type 1.

IF 2.1 Q2 ORTHOPEDICS
Fahad A Alshayhan, Reggie C Hamdy
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引用次数: 0

Abstract

Neurofibromatosis type 1 (NF-1) leads to cutaneous, neurological, and musculoskeletal manifestations. Congenital pseudarthrosis of the tibia treatment is considered aggressive in achieving bone union. Most of those patients get a short limb at the end of treatment because of pathological bone resection and malalignment. One of the manifestations that can appear in patients is localized hemihypertrophy of the limb. In our case, we present the first time a coexistence of congenital pseudarthrosis of the tibia and hemihypertrophy in the same leg was reported.

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1型神经纤维瘤病患者先天性胫骨假关节和半肥厚的重合。
1型神经纤维瘤病(NF-1)导致皮肤、神经和肌肉骨骼表现。先天性胫骨假关节治疗被认为是实现骨愈合的积极手段。大多数患者在治疗结束时由于病理性骨切除和不对齐而导致肢体短。患者可能出现的表现之一是肢体局部半肥厚。在我们的病例中,我们首次报道了同一条腿先天性胫骨假关节和半肥厚并存的情况。
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来源期刊
CiteScore
2.60
自引率
6.70%
发文量
282
审稿时长
8 weeks
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