摘要
进行性骨化性肌炎是以先天性拇趾畸形和肌健、韧带、筋膜以及骨胳肌进行性异位骨化为特征。开始为颈后、胸背部红、肿、疼痛、压痛、筋膜下结节，继而从近侧向远侧，从中轴向周围，从背侧向腹侧发展。有的结节自行缩小，有的则形成成熟的异位骨。由于继发关节外的僵直，形成严重的伤残。发病年龄在１０岁以内。根据临床特征和Ｘ线表现可以诊断。不宜活组织检查，以免促使病情恶化。
yositis
ossifcans progressive is an extremely rare disorder of differentiation that is characterized by
congenital malformation of the great toes and by progressing heterotopic ossification of thd
tendons ,ligament ,fasciae and skeletal muscle heterotopic ossification typical appears in the
first decade of life,often begining as painful ,erythematous,tender and subrfaicial nodules in the
posterior potion of the neck and in the back,then proximal -to-distal
progression,axial-to-appendicular progressionl.Indicidual nodules may regress of they
progress fo form mature heterotopic bone.Severe dissability develops secondary to
extracrrticular ankylosis of thd joints The digno-sis can be made thd basis of clinical features
and roentgenographic criteria.Biopsy is not needed to make the dignosis;biopsy uniformly
exacerdates the comdition and shoule be avoided.
出处
《颈腰痛杂志》
1995年第2期71-73,共3页
The Journal of Cervicodynia and Lumbodynia
