Vanneste J A, Augustijn P B, Stam F C
Department of Neurology, Sint Lukasziekenhuis, Amsterdam, The Netherlands.
J Neurol Neurosurg Psychiatry. 1988 Jan;51(1):131-5. doi: 10.1136/jnnp.51.1.131.
Two half-sisters aged 14 and 18 years are described with a rigid spine syndrome as the cardinal clinical feature of an autosomal dominant neuromuscular disorder. Ten years previously, a diagnosis of multicore disease had been made from the clinical signs and muscle biopsy findings. Long term follow-up revealed a non-specific muscular dystrophy with axial predominance and a rigid spine in the younger girl; the older sister presented at the age of 18 with a rigid spine as the only myopathic sign. Computed tomography of the muscles showed severe involvement of the paraspinal musculature, in contrast with either less or no involvement of the other muscles.
本文描述了两名年龄分别为14岁和18岁的同父异母姐妹,她们患有常染色体显性遗传神经肌肉疾病,主要临床特征为脊柱僵硬综合征。十年前,根据临床症状和肌肉活检结果诊断为多核病。长期随访显示,较年幼的女孩患有以轴性为主的非特异性肌营养不良症且伴有脊柱僵硬;姐姐18岁时出现脊柱僵硬,这是唯一的肌病体征。肌肉计算机断层扫描显示椎旁肌肉组织严重受累,相比之下,其他肌肉受累较少或未受累。