Idiopathic CD4 lymphocytopenia with sensorimotor polyneuropathy

被引:1
|
作者
Puri, Vinod [1 ]
Duggal, Ashish Kumar [1 ]
Chaudhry, Neera [1 ]
机构
[1] Govind Ballabh Pant Inst Post Grad Med Educ & Res, Dept Neurol, New Delhi, India
关键词
Idiopathic CD4 lymphocytopenia; immune mediated neuropathy; neuropathy; optic neuropathy; UNEXPLAINED OPPORTUNISTIC INFECTIONS; T-LYMPHOCYTOPENIA; AUTOIMMUNITY; LYMPHOPENIA; PATIENT;
D O I
10.4103/0972-2327.165470
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A, 21-years-old, male, presented with acute onset, gradually progressive, predominantly distal, symmetrical weakness of both upper and lower limbs with arreflexia. He had impaired sensations in glove and stocking distribution with distal gradient. He was found to have absolute CD4 + cell count of 188 cells/mu L, absolute CD8 cell count, 532 cells/mu L and CD4: CD8 ratio of 0.35. Electrophysiology revealed reduced to absent CMAP amplitude as well as SNAPs in various nerves of upper and lower limbs, along with normal conduction velocity and normal F wave latencies. Pattern evoked visual potentials were prolonged, on both sides, P100 being 130 ms, on right and 108 ms, on left side. In the follow up of 2 years, he showed spontaneous but gradual clinical improvement but his electrophysiological parameters as well as CD 4+ cells count did not show any significant improvement.
引用
收藏
页码:381 / 384
页数:4
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