Teive Hélio A G, de Quadros Aníbal, Barros Felipe Cabral, Werneck Lineu César
Serviço de Neurologia, Departamento de Clínica Médica, Hospital de Clínicas, Universidade Federal de Paraná, Curitiba, PR, Brasil.
Arq Neuropsiquiatr. 2002 Dec;60(4):1025-9. doi: 10.1590/s0004-282x2002000600027. Epub 2003 Jan 15.
We report the case of a 78 years old female patient with primary restless legs syndrome (RLS) with an autosomal dominant pattern of inheritance. In addition, the patient also had depression. We emphasize the worsening of symptoms of RLS after the use of a selective serotonin uptake inhibitor (mirtazapine), with improvement after the drug was discontinued, and an excellent recovery with the use of low dose dopaminergic agonist (pramipexol).
我们报告了一例78岁患有原发性不宁腿综合征(RLS)且呈常染色体显性遗传模式的女性患者。此外,该患者还患有抑郁症。我们强调使用选择性5-羟色胺再摄取抑制剂(米氮平)后不宁腿综合征症状恶化,停药后症状改善,以及使用低剂量多巴胺能激动剂(普拉克索)后实现了良好康复。