Asaka T
Department of Neurology, Kanazawa University School of Medicine, Japan.
Acta Neurol Scand. 1994 Apr;89(4):307-8. doi: 10.1111/j.1600-0404.1994.tb01686.x.
A 22-year-old male college student had a syndactyly between the second and third fingers of his left hand, which was congenitally small in size. His left pectoralis muscles were absent. He first walked at the age of 12 months, but soon developed difficulties in walking due to weakness of the legs. Atrophy and weakness of the legs aggravated gradually. He was diagnosed as having peroneal muscular atrophy and Poland syndrome, an association of which has not been reported before. A small number of similar cases of peroneal muscular atrophy with various skeletal abnormalities in the literature suggest that the association is not incidental, but of clinical significance.
一名22岁的男大学生左手第二和第三指之间有并指，且该并指先天性较小。他左侧胸肌缺失。他12个月大时开始走路，但很快因腿部无力而出现行走困难。腿部萎缩和无力逐渐加重。他被诊断为腓骨肌萎缩症和波兰综合征，此前尚未有这两种病症关联的报道。文献中少数伴有各种骨骼异常的腓骨肌萎缩症类似病例表明，这种关联并非偶然，而是具有临床意义。
