Peces Ramón, Peces Carlos, Pérez-Dueñas Virginia, Vega-Cabrera Cristina, Campos Isabel
Servicio de Nefrología , Hospital Universitario La Paz, Madrid.
Area de Tecnología de la Información, SESCAM, Toledo , Spain.
NDT Plus. 2009 Oct;2(5):360-1. doi: 10.1093/ndtplus/sfp040. Epub 2009 Apr 21.
This is the first report of a case of sacral radicular cysts in a patient with autosomal dominant polycystic kidney disease (ADPKD). A 46-year-old woman with ADPKD was found to have bilateral sacral radicular cysts discovered incidentally by magnetic resonance imaging (MRI). Cysts arising from arachnoid or spinal meningeal sac should be considered one of the manifestations of a more widespread connective tissue disorder associated with ADPKD.
这是首例关于常染色体显性遗传性多囊肾病(ADPKD)患者出现骶神经根囊肿的报告。一名患有ADPKD的46岁女性通过磁共振成像(MRI)偶然发现双侧骶神经根囊肿。源自蛛网膜或脊髓脑膜囊的囊肿应被视为与ADPKD相关的更广泛结缔组织疾病的表现之一。