Fountain Hayes B, de Monaco Bernardo A, Jagid Jonathan, Benveniste Ronald, Cordeiro Joacir G
Department of Neurological Surgery, University of Miami Miller School of Medicine, Miami, USA.
Neurosurgery, University of Sao Paulo, Sao Paulo, BRA.
Cureus. 2023 Feb 14;15(2):e34970. doi: 10.7759/cureus.34970. eCollection 2023 Feb.
Autosomal dominant polycystic kidney disease (ADPKD) is a connective tissue disease with vascular abnormalities involving multiple organs. The prevalence of ADPKD associated with a spontaneous subdural hematoma (SDH) is very low, with less than 10 cases reported in the literature to date. Symptomatic chronic SDH is classically treated with a twist drill, burr holes, or craniotomy. Recently, middle meningeal artery (MMA) embolization has emerged as an ancillary modality. We present the first case in the literature of a bilateral SDH in a young ADPKD patient successfully managed with MMA embolization. Moreover, we discuss the role of different treatment modalities on this subset of patients.
常染色体显性多囊肾病(ADPKD)是一种结缔组织疾病,伴有累及多个器官的血管异常。ADPKD合并自发性硬膜下血肿(SDH)的患病率非常低,迄今为止文献报道的病例不足10例。有症状的慢性SDH传统上采用锥颅术、钻孔术或开颅手术治疗。最近,脑膜中动脉(MMA)栓塞已成为一种辅助治疗方式。我们报告了文献中首例年轻ADPKD患者双侧SDH成功通过MMA栓塞治疗的病例。此外,我们还讨论了不同治疗方式对这一亚组患者的作用。