Bhuta Kunal, Cordova Sanchez Andres, Soipe Ayorinde, Mobeen Haris, Devkota Kriti
Department of Internal Medicine, State University of New York (SUNY) Upstate Medical University, Syracuse, USA.
Cureus. 2022 Jul 21;14(7):e27095. doi: 10.7759/cureus.27095. eCollection 2022 Jul.
Uremic neuropathy (UN) is a sensorimotor polyneuropathy typically affecting the lower extremities due to length-dependent demyelination and axonal degeneration. Hemodialysis (HD) and peritoneal dialysis (PD) are the two widely used modalities for treating end-stage renal disease (ESRD) patients. Today, with the understanding of solute and water kinetics, PD is considered equivalent to in-center HD. Chronic inflammatory demyelinating polyneuropathy (CIDP) manifests as symmetric, motor-predominant neuropathy that results in both proximal and distal muscle weakness. It is treatable with immune modulatory therapies. Here, we present a series of three patients who developed CIDP following the initiation of PD. Patient A: 39-year-old male with ESRD secondary to renal dysplasia presented with new onset neuropathy four months after starting PD. Patient B: 30-year-old male with ESRD secondary to IgA nephropathy presented with a history of numbness in his feet gradually progressing to his legs 12 months after initiating PD. Patient C: 56-year-old female with ESRD and uncontrolled diabetes mellitus presented with progressive muscle weakness four months after initiating PD. These three patients were all on continuous cycling PD. They were followed at three different dialysis units and were initiated on CCPD at different times. All of these patients were found to have CIDP on electromyography. Patients A and B were treated with IV immunoglobulin (IVIG) and improved, while patient C received plasmapheresis and improved. It has been recognized that PD solution is not physiological and may lead to activation of the host immune system triggering an autoimmune demyelinating process. Immunologic pathogenesis is not clearly understood. Macrophage activation and cytokines may play a role in the demyelination process. With the recent initiative to increase the use of PD, more studies are warranted to understand this uncommon complication.
尿毒症神经病变(UN)是一种感觉运动性多发性神经病变,通常由于长度依赖性脱髓鞘和轴突变性而累及下肢。血液透析(HD)和腹膜透析(PD)是治疗终末期肾病(ESRD)患者的两种广泛应用的方式。如今,随着对溶质和水动力学的认识,腹膜透析被认为等同于中心血液透析。慢性炎症性脱髓鞘性多发性神经病变(CIDP)表现为对称性、以运动为主的神经病变,导致近端和远端肌肉无力。它可用免疫调节疗法治疗。在此,我们报告了3例在开始腹膜透析后发生CIDP的患者。患者A:一名39岁男性,因肾发育不良继发ESRD,在开始腹膜透析4个月后出现新发神经病变。患者B:一名30岁男性,因IgA肾病继发ESRD,在开始腹膜透析12个月后出现足部麻木病史,逐渐发展至腿部。患者C:一名56岁女性,患有ESRD且糖尿病控制不佳,在开始腹膜透析4个月后出现进行性肌肉无力。这3例患者均接受持续循环腹膜透析。他们在3个不同的透析单位接受随访,并在不同时间开始接受持续非卧床腹膜透析。所有这些患者经肌电图检查均被诊断为CIDP。患者A和B接受静脉注射免疫球蛋白(IVIG)治疗后病情改善,而患者C接受血浆置换后病情改善。人们已经认识到腹膜透析液并非生理性的,可能导致宿主免疫系统激活,引发自身免疫性脱髓鞘过程。免疫发病机制尚不清楚。巨噬细胞激活和细胞因子可能在脱髓鞘过程中起作用。随着近期增加腹膜透析使用的倡议,有必要进行更多研究以了解这种罕见并发症。