Alexander S, David V G, Varughese S, Tamilarasi V, Jacob C K
Department of Nephrology, Christian Medical College, Vellore, Tamil Nadu, India.
Indian J Nephrol. 2013 Mar;23(2):137-9. doi: 10.4103/0971-4065.109439.
Posterior reversible encephalopathy syndrome (PRES) is an uncommon post-renal transplant complication. We report a 16-year-old boy who had an acute cellular rejection immediate post-transplant and was given intravenous methylprednisolone along with an increase in tacrolimus dose. He was diagnosed to have PRES based on clinical and radiological features within 6 h of intensified immunosuppression. This is an unusual case report of successfully managing PRES with continuation of the intensified immunosuppression as warranted by the clinical situation, along with aggressive blood pressure control. After 6 weeks, magnetic resonance imaging showed complete resolution of lesions. He has good graft function and no residual neurological deficits while on small doses of three antihypertensives, 12 months after transplantation.
后部可逆性脑病综合征(PRES)是一种罕见的肾移植后并发症。我们报告一名16岁男孩,他在移植后立即发生急性细胞排斥反应,接受了静脉注射甲泼尼龙并增加了他克莫司剂量。在强化免疫抑制治疗后6小时内,根据临床和影像学特征,他被诊断为患有PRES。这是一例不同寻常的病例报告,根据临床情况继续进行强化免疫抑制治疗,并积极控制血压,成功地治疗了PRES。6周后,磁共振成像显示病变完全消退。移植12个月后,他在服用小剂量三种抗高血压药物的情况下,移植肾功能良好,没有残留神经功能缺损。