Clinical Reasoning: A 28-Year-Old Man with Subacute-Onset Ataxic Gait.

IF 0.6 Q4 CLINICAL NEUROLOGY
Mauricio Benetti, Francisco Caiza-Zambrano, Ricardo Reisin, Claudia Shanley, Nicolás Roccatagliata, Luciana León-Cejas
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Abstract

The diagnostic approach to subacute progressive polyneuropathy can be challenging, particularly when accompanied by systemic features. We present a 28-year-old man with subacute-onset ataxic gait. Four months before his initial evaluation at our center, he was assessed by orthopedics for a poorly differentiated tumor of the right tibia. He also reported intermittent fever and unintentional weight loss. Neurologic examination revealed marked weakness in all four limbs, with deep tendon reflexes absent in the lower extremities. Sensory testing demonstrated a stocking-glove distribution of hypoesthesia. Vibration and proprioception were decreased in all four limbs. Romberg sign was positive, and he had a broad-based ataxic gait with bilateral steppage. Nerve conduction studies demonstrated a demyelinating sensorimotor polyneuropathy. Initial laboratory and imaging studies showed thrombocytosis and radiologic evidence of organomegaly. This case highlights a stepwise diagnostic approach to progressive polyneuropathy with red flags for systemic disease and emphasizes the importance of integrating neurologic and systemic findings to expand the differential diagnosis, guide targeted investigations, and identify potentially treatable underlying conditions.

临床推理:一个28岁的男性亚急性发作的共济失调步态。
亚急性进行性多神经病变的诊断方法具有挑战性,特别是当伴有全身特征时。我们提出一个28岁的男子亚急性发作的共济失调步态。在他在我们中心进行初次评估的四个月前,矫形科对他进行了右胫骨低分化肿瘤的评估。他还报告间歇性发烧和体重意外减轻。神经学检查显示四肢明显无力,下肢无深肌腱反射。感觉测试显示感觉减退呈长袜手套分布。四肢振动和本体感觉均减弱。Romberg征是阳性的,他有广泛的共济失调步态和双侧步。神经传导研究显示脱髓鞘感觉运动多发性神经病。最初的实验室和影像学检查显示血小板增多和器官肿大的放射学证据。本病例强调了对进行性多神经病变的分步诊断方法,并强调了将神经系统和全身检查结果结合起来扩大鉴别诊断、指导有针对性的调查和识别潜在可治疗的潜在疾病的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neurohospitalist
Neurohospitalist CLINICAL NEUROLOGY-
CiteScore
1.60
自引率
0.00%
发文量
108
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