Suppr超能文献

[米勒-魏斯病:舟骨特发性缺血性坏死]

[Müller-Weiss disease: idiopathic avascular necrosis of the navicular bone].

作者信息

Goedhart Louren M, Somford Matthijs P, Kempink Dagmar R J, Zeegers A V C M Elgun

机构信息

Medisch Spectrum Twente, afd. Orthopedie, Enschede.

出版信息

Ned Tijdschr Geneeskd. 2015;159:A9036.

Abstract

BACKGROUND

Müller-Weiss disease is a rare and complex foot disorder. The underlying aetiology of this condition involves abnormal loading of the navicular bone combined with delayed ossification. Müller-Weiss disease is progressive and ultimately results in deformation and fragmentation of the navicular bone with plantar-flexed hindfoot varus. In patients with a severe form of this foot deformity, treatment involves arthrodesis of the midfoot with bridging of the navicular bone.

CASE DESCRIPTION

A 43-year-old female patient was seen in our outpatient clinic with pain in her right foot. Her symptoms had been present for seven months and had developed spontaneously without prior trauma. Imaging investigations resulted in the diagnosis of Müller-Weiss disease in both her right and her left foot.

CONCLUSION

It is important to recognize this condition at an early stage so that patients can receive conservative treatment initially.

摘要

背景

米勒-魏斯病是一种罕见且复杂的足部疾病。这种病症的潜在病因包括舟骨异常负重以及骨化延迟。米勒-魏斯病呈进行性发展,最终会导致舟骨变形和碎裂,并伴有后足内翻跖屈。对于患有这种严重足部畸形的患者,治疗方法包括中足关节融合术并跨越舟骨。

病例描述

一名43岁女性患者因右脚疼痛前来我院门诊就诊。她的症状已持续7个月,且无先前创伤史,是自发出现的。影像学检查结果诊断她的左右脚均患有米勒-魏斯病。

结论

早期识别这种病症很重要,以便患者最初能够接受保守治疗。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验