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夏科-马里-图思病的足踝表现

Foot and ankle manifestations of Charcot-Marie-Tooth disease.

作者信息

Holmes J R, Hansen S T

机构信息

Department of Orthopaedics, University of Washington, Harborview Medical Center, Seattle.

出版信息

Foot Ankle. 1993 Oct;14(8):476-86. doi: 10.1177/107110079301400809.

Abstract

The term Charcot-Marie-Tooth disease represents a spectrum of neurological dysfunction more recently described as hereditary motor-sensory neuropathies. An abnormality of myelination is thought to be responsible for the clinical manifestations. While histological findings have been well described, the exact biochemical basis for this disorder remains unknown. Over one half of patients with Charcot-Marie-Tooth disease manifest foot and ankle problems, including pain, weakness, deformity, and, rarely, paresthesias. Characteristic patterns of neuromuscular weakness have been identified. Bilateral pes cavovarus is the most common pathologic foot deformity seen. The specific components include hindfoot varus, anterior or forefoot cavus, and, often clawtoes. The etiology of this abnormal foot posture usually results from tibialis posterior overpowering peroneus brevis coupled with peroneus longus overpowering tibialis anterior. Multiple treatment options have been described. Rationale for specific tendon transfers, soft tissue release, osteotomies, and arthrodesis is discussed. Results of surgical intervention are difficult to interpret and compare because of the wide spectrum of both neurological dysfunction and described operative procedures. In the presence of flexible deformity, early soft tissue release and tendon transfers may help prevent or delay more extensive bony procedures. The clinical results of triple arthrodesis in the Charcot-Marie-Tooth disease patient appear to deteriorate with time. Genetic transmission, progression of the neurological dysfunction, flexibility of the deformity, distribution of muscular weakness, and anticipated foot demands vary a great deal within this patient population. Treatment decisions, therefore, must be individualized and based upon a clear history, careful examination, and well-defined patient goals.

摘要

夏科-马里-图思病这一术语代表了一系列神经功能障碍,最近被描述为遗传性运动感觉神经病。髓鞘形成异常被认为是临床表现的原因。虽然组织学发现已有详细描述,但这种疾病的确切生化基础仍然未知。超过一半的夏科-马里-图思病患者表现出足踝问题,包括疼痛、无力、畸形,很少有感觉异常。已经确定了神经肌肉无力的特征性模式。双侧高弓内翻足是最常见的病理性足部畸形。具体组成部分包括后足内翻、前足或前脚掌高弓,且常伴有爪形趾。这种异常足部姿势的病因通常是胫后肌力量超过腓骨短肌,同时腓骨长肌力量超过胫前肌。已经描述了多种治疗选择。讨论了特定肌腱转移、软组织松解、截骨术和关节融合术的理论依据。由于神经功能障碍和所描述的手术操作范围广泛,手术干预的结果难以解释和比较。在存在柔韧性畸形的情况下,早期软组织松解和肌腱转移可能有助于预防或延迟更广泛的骨手术。夏科-马里-图思病患者行三关节融合术的临床结果似乎会随着时间推移而恶化。在这一患者群体中,遗传传递、神经功能障碍的进展、畸形的柔韧性、肌肉无力的分布以及预期的足部需求差异很大。因此,治疗决策必须个体化,基于清晰的病史、仔细的检查以及明确的患者目标。

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