Moise Elena-Sonia, Bratu Razvan Matei, Hanganu Andreea, Sajin Maria
Department of Pathology, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Department of Anatomy, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Diagnostics (Basel). 2022 Jul 11;12(7):1691. doi: 10.3390/diagnostics12071691.
Chronic Inflammatory Demyelinating Polyneuropathy is an immune-mediated pathology of the peripheral nerves and nerve roots that leads to weakness and sensory symptoms. Given its clinical heterogeneity, often times diagnosis is challenging. Even though nerve conduction studies and clinical features are the main criteria used for diagnosis, supplementary investigations, such as nerve biopsies, cerebral spinal fluid examination and magnetic resonance studies, may be used in order to confirm the diagnosis. Given the fact that the hallmark in CIDP physiopathology is the demyelination process, nerve biopsies are used to demonstrate and assess the magnitude of the phenomenon. The question and the main interest of this review is whether histopathological findings are relevant for the diagnosis and can be useful in disease assessment.
慢性炎症性脱髓鞘性多发性神经病是一种由免疫介导的周围神经和神经根病变,可导致肌无力和感觉症状。鉴于其临床异质性,诊断往往具有挑战性。尽管神经传导研究和临床特征是诊断的主要标准,但为了确诊,可能会采用补充检查,如神经活检、脑脊液检查和磁共振检查。鉴于CIDP病理生理学的标志是脱髓鞘过程,神经活检用于证实和评估该现象的严重程度。本综述的问题及主要关注点在于组织病理学发现是否与诊断相关,以及是否有助于疾病评估。