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从 95 例分析看 Müller-Weiss 病。

Towards understanding Müller-Weiss disease from an analysis of 95 cases.

机构信息

Department of Trauma & Orthopaedics, UK; University of Ulster, Altnagelvin Hospital, Glenshane Road, Londonderry BT47 6SB Northern Ireland, UK.

Department of Trauma & Orthopaedics, UK.

出版信息

Foot Ankle Surg. 2023 Jul;29(5):401-411. doi: 10.1016/j.fas.2023.05.004. Epub 2023 May 16.

Abstract

BACKGROUND

The single existing classification of Müller-Weiss Disease (MWD), based solely upon Méary's angle, serves neither as guide for prognosis nor treatment. This accounts for lack of gold standard in its management.

METHODS

Navicular compression, medial extrusion, metatarsal lengths, Kite's, lateral and dorsoplantar talo-first metatarsal angles were measured in 95 feet with MWD. Joints involved, presence and location of navicular fracture were recorded.

RESULTS

Group 1 "early-onset" MWD feet (n = 11) had greatest compression and medial extrusion, and lowest Kite's angles. All except 1 were index minus and had lateral navicular fracture. Only 1 had moderate degeneration at the talonavicular joint (TNJ) with none requiring surgery yet. Group 2 "Müller-Weissoid" feet (n = 23) had radiologically normal navicular in their fifties and developed MWD on average 5 years later. They had the lowest compression and extrusion, and highest Kite's angles. None had complete fracture. All had TNJ arthritis, with early changes at lateral naviculocuneiform joint (NCJ) in 43%. Group 3 "late-onset" MWD presented in the sixth decade. Only TNJ was involved in Group 3 A (n = 16). Group 3B (n = 20) affected TNJ more than NCJ and had the greatest number of Maceira stage V disease. Group 3 C "reverse Müller-Weiss disease", which affected NCJ more than TNJ (n = 25), had greatest midfoot abduction and overlength of the second metatarsal. No fracture occurred in group 3 A compared to 65% and 32% in groups 3B and 3 C, respectively.

CONCLUSIONS

With need to compare like-for-like pathology, the proposed classification provides a common platform for reporting outcomes of different treatments. We theorize pathogenetic pathways in the various groups.

摘要

背景

目前仅有基于梅里角的单一分类系统用于 Müller-Weiss 病(MWD),该分类系统既不能指导预后,也不能指导治疗。这也是导致其缺乏金标准治疗的原因。

方法

在 95 例 MWD 患者中测量舟骨压缩、内侧突出、跖骨长度、Kite 角、外侧和背跖侧距舟第一跖骨角。记录受累关节、舟骨骨折的存在和位置。

结果

第 1 组“早发性”MWD 足(n=11)的压缩和内侧突出最大,Kite 角最低。除 1 例外,其余均为指数负数且存在外侧舟骨骨折。仅有 1 例在距舟关节(TNJ)有中度退变,且目前无需手术。第 2 组“Müller-Weiss 样”足(n=23)在 50 多岁时舟骨影像学正常,平均 5 年后发展为 MWD。他们的压缩和突出最小,Kite 角最高。无完全骨折。所有患者均有 TNJ 关节炎,43%的患者外侧舟楔关节(NCJ)有早期改变。第 3 组“迟发性”MWD 出现在 60 多岁。第 3 组 A(n=16)仅累及 TNJ。第 3 组 B(n=20)累及 TNJ 多于 NCJ,Maceira 分期 V 疾病的病例数最多。第 3 组 C“反向 Müller-Weiss 病”,即 NCJ 受累多于 TNJ(n=25),中足外展最大,第二跖骨过长。第 3 组 A 中未发生骨折,而第 3 组 B 和 3 组 C 中分别有 65%和 32%发生骨折。

结论

为了比较相似的病理,本研究提出的分类为报告不同治疗结果提供了一个通用平台。我们推测了不同组别的发病机制途径。

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