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淀粉样变肌病的磁共振成像评估

MRI evaluation of amyloid myopathy.

作者信息

Metzler J P, Fleckenstein J L, White C L, Haller R G, Frenkel E P, Greenlee R G

机构信息

Department of Radiology, University of Texas Southwestern Medical Center, Dallas.

出版信息

Skeletal Radiol. 1992;21(7):463-5. doi: 10.1007/BF00190993.

Abstract

Amyloid myopathy is a rare complication of primary amyloidosis. The magnetic resonance imaging (MRI) features of two patients with amyloid myopathy were studied. Slight prolongation of muscle T1 and T2 relaxation times was evident but the striking abnormality was marked reticulation of the subcutaneous fat. The clinical findings of indurated extremities far exceeds the minimal signal intensity alteration seen in the muscles. The MR appearance of amyloid myopathy differs from that of other neuromuscular conditions in the minimal changes found in muscle, but the striking abnormality seen in subcutaneous fat makes it distinct from many neuromuscular conditions.

摘要

淀粉样变肌病是原发性淀粉样变性的一种罕见并发症。对两名淀粉样变肌病患者的磁共振成像(MRI)特征进行了研究。肌肉T1和T2弛豫时间有轻微延长,但明显的异常是皮下脂肪显著呈网状改变。肢体硬结的临床所见远远超过肌肉中所见的最小信号强度改变。淀粉样变肌病的磁共振表现与其他神经肌肉疾病不同,其在肌肉中的改变最小,但皮下脂肪的明显异常使其有别于许多神经肌肉疾病。

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