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穆勒 - 魏斯综合征中的扁平足:病例系列

Flatfoot in Müller-Weiss syndrome: a case series.

作者信息

Wang Xu, Ma Xin, Zhang Chao, Huang Jia-Zhang, Jiang Jian-Yuan

机构信息

Department of Orthopedics, Huashan Hospital, Fudan University, No, 12 Wulumuqi Middle Road, Shanghai, 200040, China.

出版信息

J Med Case Rep. 2012 Aug 1;6:228. doi: 10.1186/1752-1947-6-228.

Abstract

INTRODUCTION

Spontaneous osteonecrosis of the navicular bone in adults is a rare entity, known as Müller-Weiss syndrome. We report here on our experience with six patients with Müller-Weiss syndrome accompanied by flatfoot deformity, but on a literature search found no reports on this phenomenon. Because the natural history and treatment are controversial, an understanding of how to manage this deformity may be helpful for surgeons when choosing the most appropriate operative procedure.

CASE PRESENTATION

Six patients (five women, one man; average age, 54 years) with flatfoot caused by osteonecrosis of the navicular bone were followed up between January 2005 and December 2008 (mean follow-up period, 23.2 months). Conservative treatment, such as physical therapy, and non-steroidal anti-inflammatory drugs were used, but failed. Physical examinations revealed flattening of the medial arch of the involved foot and mild tenderness at the mid-tarsal joint. Weight-bearing X-rays (anterior-posterior and lateral views), computed tomography, and MRI scans were performed for each case. Talonavicular joint arthrodesis was performed in cases of single talonavicular joint arthritis. Triple arthrodesis was performed in cases of triple joint arthritis to reconstruct the medial arch. Clinical outcomes were assessed using the American Orthopaedic Foot and Ankle Society ankle-hindfoot scale; the scores were 63.0 pre-operatively and 89.8 post-operatively. All patients developed bony fusion.

CONCLUSIONS

The reason for the development of flatfoot in patients with Müller-Weiss syndrome is unknown. Surgical treatment may achieve favorable outcomes in terms of deformity correction, pain relief, and functional restoration. The choice of operative procedure may differ in patients with both flatfoot and posterior tibial tendon dysfunction.

摘要

引言

成人舟状骨自发性骨坏死是一种罕见病症,即米勒-魏斯综合征。我们在此报告6例伴有扁平足畸形的米勒-魏斯综合征患者的治疗经验,但经文献检索未发现关于此现象的报道。由于其自然病程和治疗方法存在争议,了解如何处理这种畸形可能有助于外科医生选择最合适的手术方式。

病例报告

2005年1月至2008年12月期间,对6例因舟状骨骨坏死导致扁平足的患者(5例女性,1例男性;平均年龄54岁)进行了随访(平均随访期23.2个月)。采用了物理治疗和非甾体类抗炎药等保守治疗方法,但均失败。体格检查发现患侧足内侧弓扁平,中跗关节轻度压痛。对每例患者均进行了负重X线检查(前后位和侧位片)、计算机断层扫描和磁共振成像扫描。对于单关节距舟关节炎患者行距舟关节融合术。对于三关节关节炎患者行三关节融合术以重建内侧弓。采用美国矫形足踝协会踝-后足评分系统评估临床疗效;术前评分为63.0,术后为89.8。所有患者均实现了骨融合。

结论

米勒-魏斯综合征患者出现扁平足的原因尚不清楚。手术治疗在矫正畸形、缓解疼痛和恢复功能方面可能取得良好效果。对于同时患有扁平足和胫后肌腱功能障碍的患者,手术方式的选择可能有所不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/724f/3459784/13a7a6c30f4d/1752-1947-6-228-1.jpg

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