Atypical presentations of Lhermitte's sign after treatment for human papillomavirus-associated oropharyngeal squamous cell carcinoma.

IF 0.4 Q3 MEDICINE, GENERAL & INTERNAL
Alifya Altaf Lokhandwala, Jonathan Paly, Thomas Roberts, Jong Chul Park, Manisha Patel, Lori Wirth, Gilbert Youssef, Jennifer L Powers, Ross D Merkin
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引用次数: 0

Abstract

Lhermitte's sign (LS) is characterised by a brief electric shock-like sensation elicited by neck flexion that radiates down the spine and may extend into the posterior aspects of the legs. It is a clinical indicator of cervical or upper thoracic dorsal column dysfunction, most commonly due to demyelination or intrinsic spinal cord pathology. It may occur after head and neck (chemo)radiotherapy. We describe two patients with human papillomavirus-associated oropharyngeal squamous cell carcinoma who developed LS following chemoradiotherapy. One patient developed protracted LS lasting 20 months beyond completion of definitive concurrent chemoradiotherapy with volumetric modulated arc radiotherapy and weekly cisplatin and another patient developed protracted LS after adjuvant de-escalated volumetric modulated arc radiotherapy lasting 12 months beyond treatment completion. These cases show the variable course of LS in the modern conformal era and highlight its benign prognosis but potential for persistent symptoms that affect patient quality of life.

人乳头瘤病毒相关口咽鳞状细胞癌治疗后Lhermitte症状的不典型表现
Lhermitte症候群(LS)的特征是颈部弯曲引起的短暂的类似电击的感觉,这种感觉向下辐射到脊柱,并可能延伸到腿的后部。它是颈椎或上胸背柱功能障碍的临床指标,最常见的原因是脱髓鞘或内在脊髓病理。它可能发生在头颈部(化疗)放疗后。我们描述了两例人乳头瘤病毒相关口咽鳞状细胞癌患者在放化疗后发展为LS。一名患者在完成明确的同步放化疗(包括体积调节弧线放疗和每周一次顺铂)后出现了持续20个月的迟发性LS,另一名患者在辅助降糖体积调节弧线放疗后持续12个月出现了迟发性LS。这些病例显示了LS在现代适形时代的可变病程,并强调其预后良好,但潜在的持续症状影响患者的生活质量。
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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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