Paterakis Konstantinos, Brotis Alexandros, Kalogeras Adamantios, Karagianni Maria, Spiliotopoulos Theodosios, Arvaniti Christina, Petsiti Argiro, Vlychou Marianna, Dardiotis Efthimios, Arnaoutoglou Eleni, Fountas Kostas N
Department of Neurosurgery, University Hospital of Larissa, School of Medicine, University of Thessaly, 41500 Larissa, Greece.
Department of Anesthesiology, University Hospital of Larissa, 41334 Larissa, Greece.
Brain Sci. 2025 Mar 12;15(3):296. doi: 10.3390/brainsci15030296.
: End-stage renal failure (ESRF) patients are at an increased risk of various neurological complications, particularly after hemodialysis. The current case report describes a rare presentation of spontaneous intracranial hypotension (SIH) in a patient with ESRF caused by systemic lupus erythematosus (SLE). We present our case report. We also performed a systematic literature search in PubMed, Scopus, and Dimensions for the current literature review. : A total of 296 unique articles were identified, and their full text was retrieved. However, only one case report was relevant to our study and is summarized thereunder. The treatment approach involved high-dose intravenous steroids, surgical evacuation of the cranial subdural collections, and epidural blood patches to seal the presumed dural defect. : This case report describes a rare presentation of SIH in a young patient with ESRF due to SLE. Diagnostic imaging revealed extensive subdural and epidural fluid collections in the brain and spinal cord, respectively, along with a few T2 FLAIR hyperintensities noted in the right thalamus, left cerebellar hemisphere, and right occipital gyrus that subsequently resolved. The treatment approach involved high-dose intravenous steroids, surgical evacuation of the cranial subdural collections, and epidural blood patches to seal the presumed dural defect.
终末期肾衰竭(ESRF)患者出现各种神经并发症的风险增加,尤其是在血液透析后。本病例报告描述了一名由系统性红斑狼疮(SLE)导致ESRF的患者罕见的自发性颅内低压(SIH)表现。我们展示我们的病例报告。我们还在PubMed、Scopus和Dimensions中进行了系统的文献检索以进行当前的文献综述。共识别出296篇独特的文章,并检索了它们的全文。然而,只有一篇病例报告与我们的研究相关,总结如下。治疗方法包括大剂量静脉注射类固醇、手术清除颅内硬膜下积液以及硬膜外血贴以封闭推测的硬脑膜缺损。本病例报告描述了一名因SLE导致ESRF的年轻患者罕见的SIH表现。诊断性影像学检查分别显示脑内广泛的硬膜下积液和脊髓硬膜外积液,同时在右侧丘脑、左侧小脑半球和右侧枕叶回发现一些T2 FLAIR高信号,这些高信号随后消失。治疗方法包括大剂量静脉注射类固醇、手术清除颅内硬膜下积液以及硬膜外血贴以封闭推测的硬脑膜缺损。