Roy Ujjawal, Srivastava Achal Kumar, Cartwright Michael S, Panwar Ajay, Harsh Viraat
Senior Consultant, Department of Neurology, Roy Neuro Care Centre, Ranchi, India.
Professor, Department of Neurology, All India Institute of Medical Sciences, New Delhi, India.
Neuromuscul Disord. 2025 Jan;46:105243. doi: 10.1016/j.nmd.2024.105243. Epub 2024 Nov 15.
Neuromyotonia or Isaacs syndrome is a rare neuromuscular disorder secondary to hyperexcitable peripheral nerves which fire continuously causing motor unit activation and manifests clinically as cramps, muscle twitches, or visible muscle contraction associated with impaired muscle relaxation. Clinical suspicion and subsequent diagnostic work-up, including electrophysiology, aid in the diagnosis. However, when contractions are not appreciated clinically, there is a high possibility of misdiagnosis. Misdiagnosis may also be attributable to a lack of knowledge of symptoms among physicians and a paucity of diagnostic modalities, hence additional tools have been sought. Here we present the case of 15-year-old girl who presented to us with complaints of painful posturing and stiffness of both hands, which was initially diagnosed and managed as dystonia without symptomatic relief. We suspected the diagnosis of neuromyotonia only after we performed neuromuscular ultrasound, which became the main guiding light to reach the diagnosis.
神经性肌强直或艾萨克斯综合征是一种罕见的神经肌肉疾病,继发于外周神经兴奋性过高,神经持续放电导致运动单位激活,临床症状表现为痉挛、肌肉抽搐或可见的肌肉收缩,并伴有肌肉松弛受损。临床怀疑及后续包括电生理检查在内的诊断性检查有助于确诊。然而,当临床上未察觉到肌肉收缩时,误诊的可能性很高。误诊也可能归因于医生对症状认识不足以及诊断方法有限,因此人们一直在寻求更多的诊断工具。在此,我们报告一例15岁女孩的病例,她因双手疼痛性姿势异常和僵硬前来就诊,最初被诊断为肌张力障碍并进行相应治疗,但症状未缓解。直到我们进行了神经肌肉超声检查后,才怀疑是神经性肌强直,而这一检查成为确诊的主要指引。