Tănăsescu R, Ticmeanu Marina, Cojocaru Inimioara Mihaela, Luca Dimela, Nicolau Adriana, Hristea Adriana, Băicuş C
University of Medicine and Pharmacy Carol Davila, Bucharest, Romania.
Rom J Intern Med. 2008;46(3):199-205.
At the crossover of specialties, the osmotic demyelination syndromes are under-diagnosed clinical entities. Even if the knowledge and the management of these entities have evolved in the latest years, many issues are still unsolved. Initially described as diseases affecting alcoholics and malnourished and considered affecting solely the pons, it is now known that osmotic demyelination can produce extrapontine lesions (extrapontine myelinolysis). Rapid correction of sodium in hyponatremic patients is pathogenically involved in the genesis of central pontine and extrapontine myelinolysis. The aim of this review is to focus on the main characteristics of the disease, which can represent a challenge for the clinicians in respect to its recognition and treatment.
在专业交叉领域,渗透性脱髓鞘综合征是临床诊断不足的疾病实体。尽管近年来对这些疾病实体的认识和治疗方法有所进展,但许多问题仍未解决。最初这些疾病被描述为影响酗酒者和营养不良者的疾病,且被认为仅累及脑桥,现在已知渗透性脱髓鞘可产生脑桥外病变(脑桥外髓鞘溶解)。低钠血症患者血钠的快速纠正与中央脑桥和脑桥外髓鞘溶解的发生机制有关。本综述的目的是聚焦于该疾病的主要特征,这些特征在其识别和治疗方面可能对临床医生构成挑战。