胫骨和腓骨骨折后同时出现屈伸格氏畸形:一例罕见病例,同时进行手术治疗。

Kunihiko Arakawa, Youichi Yasui, Hirotaka Kawano, Wataru Miyamoto
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引用次数: 0

摘要

躅趾的格氏畸形通常表现为踝关节背屈时第一跖趾关节僵硬屈曲,但踝关节跖屈时具有灵活性,这可以被命名为屈曲格氏畸形,而伸展格氏畸形是一种罕见的情况,表现为踝关节跖屈时第一跖趾关节僵硬伸展,而踝关节背屈时具有灵活性。但是,屈伸并存的格氏畸形尚未见报道。患者是一名 27 岁的男性,在胫骨和腓骨骨折 3 年后转到我科,在之前的医院接受了切开复位和内固定治疗。他的主诉是疼痛和患侧大脚趾跖屈功能受损。诊断结果显示,该患者患有双核畸形,其特点是由于骨折后拇长屈肌(FHL)和拇长伸肌(EHL)肌腱粘连,导致拇趾屈伸同时僵硬。患者接受了手术治疗,包括使用后足内窥镜横断FHL肌腱,并将EHL肌腱转移到伸拇长肌上,手术取得了成功,术后未出现并发症。术后两年,患者的预后良好。本报告是首例有记录的双足畸形病例,强调了考虑这种情况的重要性以及手术干预的潜在优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Simultaneous flexion and extension checkrein deformity following tibial and fibular fractures: a rare case treated with concomitant surgical intervention.

Checkrein deformity of the hallux is commonly characterized by rigid flexion of the interphalangeal joint in ankle dorsiflexion but with flexibility in ankle plantarflexion which can be named as flexion checkrein deformity and as rare condition, extension checkrein deformity, characterized by rigid extension of the first metatarsophalangeal joint in ankle plantarflexion and flexibility in ankle dorsiflexion, has been reported. However, there has not reported coexistence of flexion and extension checkrein deformity. The patient, a 27-year-old male, was referred to our department 3 years after tibial and fibular fractures which was treated by open reduction and internal fixation at a previous hospital. His chief complaint was pain and impaired plantarflexion of the affected great toe. The diagnosis was double checkrein deformity characterized by simultaneous rigidity in both flexion and extension of the hallux due to the adhesion of the flexor hallucis longus (FHL) muscle and the extensor hallucis longus (EHL) tendon after a fracture. Surgical intervention was performed, which involved the transection of the FHL tendon using hindfoot endoscopy and transfer of the EHL to the extensor digitorum longus, resulting in a successful outcome with no postoperative complications. The patient demonstrated a favorable prognosis 2 years after the procedure. This report represents the first documented case of double checkrein deformity and underscores the importance of considering this condition and the potential advantages of surgical intervention.

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