原发性神经淋巴瘤,表现为斜视和复视。

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Shiny Joy, Rohit Bhatia, Shariq Ahmad Shah, Mamta Bhushan Singh, Shailesh B Gaikwad, Vaishali Suri, Raghav Singla, Sameer Bakhshi
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引用次数: 0

摘要

男性,25岁左右,有5个月的双侧下肢无力和消瘦史,同时伴有膀胱症状和勃起功能障碍。此外,他还患有双眼复视和双眼睑进行性下垂。他的临床表现提示双侧第三颅神经受累并伴有腰骶部多神经根病。最初用类固醇治疗疑似特发性腰骶部多神经根病综合征无效,因为他的症状逐渐恶化,没有其他全身性表现。我们诊断了一种罕见且可治疗的神经系统疾病,原发性神经淋巴瘤,表现为腰骶部多神经根病伴双侧第三脑神经受累。只有在神经根活检后才能确定明确的诊断,强调活检在确认诊断中的关键作用。我们的病例强调了早期考虑侵入性神经根活检的重要性,可以及时治疗并改善预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary neurolymphomatosis presenting as paraparesis and diplopia in a young man.

A man in his mid-20s presented with a 5-month history of bilateral lower limb weakness and wasting along with bladder symptoms and erectile dysfunction. Additionally, he had binocular diplopia and progressive drooping of both eyelids. His clinical presentation was suggestive of bilateral third cranial nerve involvement with lumbosacral polyradiculopathy. Initial treatment with steroids for suspected idiopathic lumbosacral polyradiculopathy syndrome proved ineffective, as his symptoms progressively worsened without other systemic manifestations. We diagnosed a rare and treatable neurological condition, primary neurolymphomatosis, presenting as lumbosacral polyradiculopathy with bilateral third cranial nerve involvement. A definitive diagnosis was established only after nerve root biopsy, highlighting the crucial role of biopsy in confirming the diagnosis. Our case underscores the importance of early consideration for an invasive nerve root biopsy, enabling prompt treatment and an improved prognosis.

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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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