Mussini J M, Mathé J F, Prost A, Gray F, Labat J J, Fève J R
Rev Neurol (Paris). 1982;138(1):25-37.
A case of rigid spine syndrome in a woman is reported. There were a diffuse myopathic process, with atrophy and mild weakness not involving the face and a major rigidity of the spine. Contractures were present as well as a pure restrictive respiratory failure. Heart-rythm disorders and prolapse of the mitral valve were present. Histological features of a deltoid muscle biopsy were slight necrosis, lack of fibrosis and major disproportion in fiber-types. There were a high rate of fiber I and absence of fiber IIB. This case was similar to others described as Dubowitz's rigid spine syndrome. The histological features belonged to the second neuropathological group of cases, with disproportion in fiber-types. The rigid spine syndrome may be considered as a clinically definite disease and distinguished from other myopathies with orthopedic deformations. It should not be confused with arthrogryposis multiplex. The disease is probably autosomic recessive.
报告了一例女性的僵硬脊柱综合征病例。存在弥漫性肌病过程,伴有萎缩和轻度肌无力,但不涉及面部,且脊柱严重僵硬。存在挛缩以及单纯的限制性呼吸衰竭。存在心律失常和二尖瓣脱垂。三角肌活检的组织学特征为轻度坏死、缺乏纤维化以及纤维类型严重不均衡。I型纤维比例高且无IIB型纤维。该病例与其他被描述为杜波维茨僵硬脊柱综合征的病例相似。组织学特征属于纤维类型不均衡的第二组神经病理学病例。僵硬脊柱综合征可被视为一种临床确诊疾病,并与其他伴有骨科畸形的肌病相区分。不应将其与多发性关节挛缩症相混淆。该疾病可能为常染色体隐性遗传。