Sobell Department of Motor Neuroscience and Movement Disorders, University College London (UCL) Institute of Neurology, London, United Kingdom.
Mov Disord. 2013 Sep;28(10):1325-9. doi: 10.1002/mds.25490. Epub 2013 Jun 4.
Back arching was reported in one of the very first patients with neurodegeneration with brain iron accumulation syndrome (NBIAs) published in 1936. However, recent reports have mainly focused on the genetic and imaging aspects of these disorders, and the phenotypic characterization of the dystonia has been lost. In evaluating patients with NBIAs in our centers, we have observed that action-induced dystonic opisthotonus is a common and characteristic feature of NBIAs. Here, we present a case series of patients with NBIAs presenting this feature demonstrated by videos. We suggest that dystonic opisthotonus could be a useful "red flag" for clinicians to suspect NBIAs, and we discuss the differential diagnosis of this feature. This would be particularly useful in identifying patients with NBIAs and no iron accumulation as yet on brain imaging (for example, as in phospholipase A2, group IV (cytosolic, calcium-independent) [PLA2G6]-related disorders), and it has management implications.
早在 1936 年就有报道称,首例神经退行性脑铁沉积综合征(NBIAs)患者出现了脊柱后凸。然而,最近的报道主要集中在这些疾病的遗传和影像学方面,而扭转痉挛的表型特征已经消失。在我们中心评估 NBIAs 患者时,我们观察到,运动诱发的痉挛性角弓反张是 NBIAs 的常见且特征性表现。在此,我们通过视频展示了一组具有这种特征的 NBIAs 患者的病例系列。我们建议,痉挛性角弓反张可能是临床医生怀疑 NBIAs 的有用“警示标志”,并讨论了该特征的鉴别诊断。这对于识别尚未出现脑影像学铁沉积的 NBIAs 患者(例如,磷脂酶 A2,第四组(胞质,钙非依赖性)[PLA2G6]相关疾病)尤为有用,并且具有管理意义。