Dima Alina, Dumitrescu Laura, Berza Ioana, Balea Marius Ioan, Mujdaba-Elmi Ayghiul, Popescu Bogdan Ovidiu, Baicus Cristian
Second Department of Internal Medicine, Colentina Clinical Hospital, Bucharest, Romania.
Second Department of Neurology, Colentina Clinical Hospital, Bucharest, Romania.
Maedica (Bucur). 2016 Mar;11(1):61-63.
Bilateral phrenic neuropathy is a rare cause of acute ventilatory failure posing both diagnostic and therapeutic difficulties. We report the case of a 55-years-old diabetic male presenting with acute onset orthopnea. Clinical and radioscopic evaluations suggested bilateral diaphragmatic paralysis, electroneuromyographic studies revealed bilateral acute phrenic neuropathy, and cerebrospinal fluid examination found albuminocytologic dissociation. The administration of high-dose intravenous immunoglobulin was followed by prompt improvement. During the next months the symptoms continued to regress. There were no recurrences. We consider the patient had a spatially limited form of acute inflammatory demyelinating polyradiculoneuropathy. The case underlies the importance of considering an immune mediated etiology in patients with acute bilateral phrenic neuropathy. To the best of our knowledge no similar case has been reported.
双侧膈神经病变是急性呼吸衰竭的罕见病因,在诊断和治疗上均存在困难。我们报告一例55岁糖尿病男性患者,以急性发作的端坐呼吸为表现。临床和影像学评估提示双侧膈肌麻痹,神经电生理检查显示双侧急性膈神经病变,脑脊液检查发现蛋白细胞分离。给予大剂量静脉注射免疫球蛋白后症状迅速改善。在接下来的几个月里,症状持续缓解。未出现复发。我们认为该患者患有一种空间局限性的急性炎症性脱髓鞘性多发性神经根神经病。该病例强调了在急性双侧膈神经病变患者中考虑免疫介导病因的重要性。据我们所知,尚无类似病例报道。