Rothe M J, Rivas R, Gould E, Kerdel F A
Department of Dermatology and Cutaneous Surgery, University of Miami School of Medicine, Florida.
Int J Dermatol. 1989 Dec;28(10):657-60. doi: 10.1111/j.1365-4362.1989.tb02436.x.
A case of scleromyxedema with associated rhabdomyolysis is reported. This appears to be a well-documented, although rare complication of scleromyxedema. This case is unique in that mucin was demonstrated in the muscle as well as the skin, and spontaneous resolution of the rhabdomyolysis occurred with the implementation of IV fluids and bed rest.
报告了一例伴有横纹肌溶解症的硬化性黏液水肿病例。这似乎是一例有充分文献记载的、尽管罕见的硬化性黏液水肿并发症。该病例的独特之处在于,在肌肉和皮肤中均发现了黏蛋白,并且通过静脉输液和卧床休息,横纹肌溶解症得以自发缓解。