Muscle MRI in neutral lipid storage disease with myopathy carrying mutation c.187+1G>A

作者：Xu, Chunxiao; Zhao, Yawen; Liu, Jing; Zhang, Wei^*; Wang, Zhaoxia; Yuan, Yun

来源：Muscle & Nerve, 2015, 51(6): 922-927.

DOI：10.1002/mus.24507

• adipose triglyceride lipase gene
• magnetic resonance imaging
• mutation c
• 187+1G > A
• myopathy
• neutral lipid storage disease
• patatin-like phospholipase domain-containing 2

IntroductionWe describe the clinical and muscle MRI changes in 2 siblings with neutral lipid storage disease with myopathy (NLSDM) carrying the mutation c.187+1G>A. @@@ MethodsPeripheral blood smears, genetic tests, and muscle biopsies were performed. Thigh MRI was performed to observe fatty replacement, muscle edema, and muscle bulk from axial sections. @@@ ResultsBoth siblings had similar fatty infiltration and edema. T1-weighted images of the gluteus maximus, adductor magnus, semitendinosus, and semimembranosus revealed marked and diffuse fatty infiltration. There was asymmetric involvement in biceps femoris and quadriceps. There was extensive fatty infiltration in the quadriceps, except for the rectus femoris. Gracilis and sartorius were relatively spared. Thigh muscle volume was decreased, while the gracilis and sartorius appeared to show compensatory hypertrophy. @@@ ConclusionsCompared with previous reports in NLSDM, MRI changes in this myopathy tended to be more severe. Asymmetry and relatively selective fatty infiltration were characteristics. Muscle Nerve51: 922-927, 2015

• 出版日期2015-6
• 单位北京大学