Haymon M, Willis R B, Ehlayel M S, Lacassie Y
Department of Radiology, Children's Hospital, New Orleans, Louisiana, USA.
Pediatr Radiol. 1997 May;27(5):415-8. doi: 10.1007/s002470050158.
Satoyoshi syndrome is a rare disorder of unknown etiology characterized by progressive, painful intermittent muscle spasms, severe skeletal abnormalities mimicking a skeletal dysplasia, malabsorption, alopecia, and amenorrhea. We further report on a 20 1/2-year-old Caucasian woman with characteristic manifestations of the syndrome. Since the establishment of the diagnosis 1 year ago, she has been treated with prednisone with good response. However, treatment of the multiple deformities and fractures has been difficult and challenging. The early recognition and treatment of this disorder is of utmost importance, as the skeletal deformities and fractures seem to be secondary to the muscular spasms, as suggested by Satoyoshi.
里吉综合征是一种病因不明的罕见疾病,其特征为进行性、疼痛性间歇性肌肉痉挛、类似骨骼发育异常的严重骨骼畸形、吸收不良、脱发和闭经。我们进一步报告一名20岁半的白种女性,她具有该综合征的典型表现。自1年前确诊以来,她接受了泼尼松治疗,反应良好。然而,对多种畸形和骨折的治疗一直困难且具有挑战性。正如里吉所指出的,由于骨骼畸形和骨折似乎继发于肌肉痉挛,因此对这种疾病的早期识别和治疗至关重要。