常染色体显性遗传性多囊肾病的疼痛评估与管理。
Evaluation and management of pain in autosomal dominant polycystic kidney disease.
机构信息
Department of Medicine, Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN 55905, USA.
出版信息
Adv Chronic Kidney Dis. 2010 May;17(3):e1-e16. doi: 10.1053/j.ackd.2010.01.005.
Abstract
Transient episodes of pain are common in autosomal dominant polycystic kidney disease (ADPKD). A small fraction of patients have disabling chronic pain. In this review, we discuss the etiologies of pain in ADPKD; review how ADPKD patients should be assessed; and discuss medical, surgical, and other management options.
摘要
常染色体显性多囊肾病（ADPKD）患者常出现短暂性疼痛发作。少数患者存在致残性慢性疼痛。在本篇综述中，我们讨论了 ADPKD 患者疼痛的病因；回顾了 ADPKD 患者的评估方法；并讨论了药物、手术和其他治疗选择。
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