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肌原纤维肌病中不同的肌肉成像模式。

Distinct muscle imaging patterns in myofibrillar myopathies.

作者信息

Fischer D, Kley R A, Strach K, Meyer C, Sommer T, Eger K, Rolfs A, Meyer W, Pou A, Pradas J, Heyer C M, Grossmann A, Huebner A, Kress W, Reimann J, Schröder R, Eymard B, Fardeau M, Udd B, Goldfarb L, Vorgerd M, Olivé M

机构信息

Department of Neurology, University Hospital Basel, Switzerland.

出版信息

Neurology. 2008 Sep 2;71(10):758-65. doi: 10.1212/01.wnl.0000324927.28817.9b.

Abstract

OBJECTIVE

To compare muscle imaging findings in different subtypes of myofibrillar myopathies (MFM) in order to identify characteristic patterns of muscle alterations that may be helpful to separate these genetic heterogeneous muscular disorders.

METHODS

Muscle imaging and clinical findings of 46 patients with MFM were evaluated (19 desminopathy, 12 myotilinopathy, 11 filaminopathy, 1 alphaB-crystallinopathy, and 3 ZASPopathy). The data were collected retrospectively in 43 patients and prospectively in 3 patients.

RESULTS

In patients with desminopathy, the semitendinosus was at least equally affected as the biceps femoris, and the peroneal muscles were never less involved than the tibialis anterior (sensitivity of these imaging criteria to detect desminopathy in our cohort 100%, specificity 95%). In most of the patients with myotilinopathy, the adductor magnus showed more alterations than the gracilis muscle, and the sartorius was at least equally affected as the semitendinosus (sensitivity 90%, specificity 93%). In filaminopathy, the biceps femoris and semitendinosus were at least equally affected as the sartorius muscle, and the medial gastrocnemius was more affected than the lateral gastrocnemius. The semimembranosus mostly showed more alterations than the adductor magnus (sensitivity 88%, specificity 96%). Early adult onset and cardiac involvement was most often associated with desminopathy. In patients with filaminopathy, muscle weakness typically beginning in the 5th decade of life was mostly pronounced proximally, while late adult onset (>50 years) with distal weakness was more often present in myotilinopathy.

CONCLUSIONS

Muscle imaging in combination with clinical data may be helpful for separation of distinct myofibrillar myopathy subtypes and in scheduling of genetic analysis.

摘要

目的

比较不同亚型的肌原纤维肌病(MFM)的肌肉影像学表现,以识别可能有助于区分这些遗传异质性肌肉疾病的肌肉改变特征模式。

方法

对46例MFM患者的肌肉影像学和临床资料进行评估(19例结蛋白病、12例肌联蛋白病、11例细丝蛋白病、1例αB-晶状体蛋白病和3例ZASP病)。43例患者的数据为回顾性收集,3例患者的数据为前瞻性收集。

结果

在结蛋白病患者中,半腱肌与股二头肌受影响程度至少相同,腓骨肌受累程度从不低于胫骨前肌(在我们的队列中,这些影像学标准检测结蛋白病的敏感性为100%,特异性为95%)。在大多数肌联蛋白病患者中,大收肌的改变比股薄肌更多,缝匠肌与半腱肌受影响程度至少相同(敏感性90%,特异性93%)。在细丝蛋白病中,股二头肌和半腱肌与缝匠肌受影响程度至少相同,腓肠肌内侧头比外侧头受累更严重。半膜肌的改变大多比大收肌更多(敏感性88%,特异性96%)。早发成年期和心脏受累最常与结蛋白病相关。在细丝蛋白病患者中,通常在生命的第五个十年开始的肌无力大多在近端明显,而在肌联蛋白病中更常出现成年晚期发病(>50岁)且伴有远端肌无力。

结论

肌肉影像学结合临床数据可能有助于区分不同的肌原纤维肌病亚型并安排基因分析。

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