Deng Lixia, Lin Yi, Lin Yu, Huang Weibin
Department of Neurology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China.
Department of Neurology, The Third Hospital of Xiamen, Xiamen, Fujian, China.
Front Neurosci. 2024 Feb 16;18:1373358. doi: 10.3389/fnins.2024.1373358. eCollection 2024.
To investigate the etiology, clinical manifestations, imaging features, and treatment of patients with infratentorial superficial siderosis (iSS), enhance clinicians' comprehension of this rare disease, and conduct oral deferiprone intervention and subsequent monitoring.
Six patients diagnosed with iSS based on magnetic resonance imaging (MRI) and susceptibility weighted imaging (SWI) were enrolled from 2021 to 2023 at the First Affiliated Hospital of Fujian Medical University. Their clinical datas were summarized, and the etiology and imaging characteristics were analyzed. Follow-up was conducted through telephone or outpatient visits.
Among the 6 patients, there were 3 males and 3 females. The onset age ranged from 35 to 71 years, with an average onset age of 53 years. The clinical symptoms mainly included acoustic disturbances (6/6), gait imbalance (6/6), dysolfactory (6/6), cognitive impairment (2/6), epilepsy (2/6), and pyramidal tract sign (2/6). Evidence of superficial siderosis was observed on MRI across the cortex, brainstem, cerebellum, and spinal cord in all patients. T2-space sequence MRI revealed two instances of dural tear. During the follow-up period ranging from 1 month to 3 years, three patients who received oral deferiprone treatment showed improvement, whereas the remaining three patients who declined deferiprone treatment demonstrated progression.
The primary clinical manifestations of iSS include bilateral sensorineural hearing disturbances, progressive cerebellar ataxia, and spinal cord lesions. The key diagnostic criteria involve the presence of linear hypointensity on T2-WI in the surface region of the nervous system. Dural tear caused by various factors is considered to be the most common cause of iSS, and its treatment mainly involves surgical intervention for hemorrhagic primary diseases as well as pharmacotherapy with deferiprone.
探讨幕下浅表性铁沉积症(iSS)患者的病因、临床表现、影像学特征及治疗方法,提高临床医生对这种罕见疾病的认识,并进行口服去铁酮干预及后续监测。
2021年至2023年在福建医科大学附属第一医院纳入6例经磁共振成像(MRI)和磁敏感加权成像(SWI)诊断为iSS的患者。总结其临床资料,分析病因及影像学特征。通过电话或门诊进行随访。
6例患者中,男性3例,女性3例。发病年龄为35至71岁,平均发病年龄为53岁。临床症状主要包括听觉障碍(6/6)、步态失衡(6/6)、嗅觉障碍(6/6)、认知障碍(2/6)、癫痫(2/6)和锥体束征(2/6)。所有患者的MRI均显示皮质、脑干、小脑和脊髓存在浅表性铁沉积证据。T2加权序列MRI显示2例硬脑膜撕裂。在1个月至3年的随访期内,3例接受口服去铁酮治疗的患者病情改善,而其余3例拒绝去铁酮治疗的患者病情进展。
iSS的主要临床表现包括双侧感音神经性听力障碍、进行性小脑共济失调和脊髓病变。关键诊断标准是神经系统表面区域T2加权像上出现线性低信号。各种因素导致的硬脑膜撕裂被认为是iSS最常见的病因,其治疗主要包括对出血性原发性疾病的手术干预以及去铁酮药物治疗。