Diagnostic uncertainty of steroid-modified Marburg's variant of multiple sclerosis even at autopsy: A case suggesting lymphoma and related myelin loss [0.03%]
类固醇治疗的Marburg变异型多发性硬化诊断不确定性甚至在尸体解剖时亦然：一例提示淋巴瘤及继发脱髓鞘病变的情况
Akira Hanazono,Keita Yasuda,Hinako Shimada et al.
Akira Hanazono et al.
MS (multiple sclerosis) has specific criteria to avoid misdiagnosis. However, the Marburg variant of MS is so fulminant that initial axonal damage and other atypical observations have been allowed in past reports. We present a 74-year-old a...
Case Reports
eNeurologicalSci. 2024 Jul 11:36:100515. DOI:10.1016/j.ensci.2024.100515 2024
Successful use of intra venous tenecteplase for acute ischemic stroke in pregnancy [0.03%]
妊娠期急性缺血性卒中成功使用静脉内替奈普酶治疗
Balamurugan Namasivayam,Chitra Sengodan,Lavanya Mohanasundaram et al.
Balamurugan Namasivayam et al.
Intravenous thrombolysis (IVT) with tenecteplase or alteplase is the standard of care in, patients with Acute Ischemic Stroke (AIS) presenting within 3-4.5 h. However here, are no established guidelines for such treatment during pregnancy. ...
Case Reports
eNeurologicalSci. 2024 Jun 19:36:100510. DOI:10.1016/j.ensci.2024.100510 2024
Effects of vaccination on COVID-19 infection symptoms in multiple sclerosis patients [0.03%]
疫苗接种对多发性硬化症患者感染新冠肺炎症状的影响
Parisa Sharifi,Nasim Rezaeimanesh,Amir Moradi et al.
Parisa Sharifi et al.
Background: Patients with multiple sclerosis (MS) are at higher risk of having infections due to receiving disease modifying therapies. The current study was conducted among Iranian MS patients who had experienced at leas...
Acute Motor Conduction Block Neuropathy After Initiation of Omalizumab: Case Report and Literature Review for Possible Causality [0.03%]
奥马珠单抗治疗后急性运动轴索性神经病1例及因果关系分析文献复习
Hosna S Elshony,Abdulaziz Al-Ghamdi
Hosna S Elshony
Background: Omalizumab is an established therapy for allergic conditions, yet its neurological effects remain underexplored compared to other biological agents. ...
Case Reports
eNeurologicalSci. 2024 Jun 15:36:100512. DOI:10.1016/j.ensci.2024.100512 2024
Is endocrine surveillance important in the care of Duchenne Muscular Dystrophy? Results from a national survey to patients and families on endocrine complications [0.03%]
Duchenne肌营养不良症的内分泌监护重要吗？对患者的全国调查结果：内分泌并发症
Despoina Galetaki,Vivian Szymczuk,Melody Shi et al.
Despoina Galetaki et al.
Glucocorticoids are standard of care for patients with Duchenne muscular dystrophy (DMD). Although prolonged exposure is associated with multiple endocrine side effects, current guidelines related to monitoring and management of endocrinopa...
Shoko Ota,Kazuo Kakinuma,Wataru Narita et al.
Shoko Ota et al.
Some patients with primary progressive aphasia (PPA) demonstrate only anomia. The lack of longitudinal observations of anomic PPA precluded us from determining whether progressive anomic aphasia was simply an early stage of semantic or logo...
Case Reports
eNeurologicalSci. 2024 Jun 6:35:100508. DOI:10.1016/j.ensci.2024.100508 2024
A case of chronic progressive autoimmune GFAP astrocytopathy with extensive meningoencephalomyelitis and contrast enhancement on MRI [0.03%]
一例慢性进行性自身免疫性胶质纤维酸性蛋白星形胶质细胞病合并广泛脑膜脑脊髓炎和磁共振成像增强的病例报告
Hironori Oka,Takumi Nakamura,Takashi Sugawara et al.
Hironori Oka et al.
•We herein present a case of chronic progressive autoimmune GFAP astrocytopathy.•Symmetrical high-intensity signals on FLAIR were observed in the white matter of the temporal and occipital lobes, lateral cerebral ventricle walls, hippocam...
Unforeseen effects: Hiccups unveiled by high-dose steroids in demyelination [0.03%]
意想不到的效应：高剂量激素导致脱髓鞘疾病出现打嗝现象
Sai Niharika Tammineedi,Ramit Singla,Marilhia Cornejo Leon et al.
Sai Niharika Tammineedi et al.
Background: Intractable hiccups, persisting beyond 48 h, pose a clinical challenge, particularly in demyelinating diseases like Neuromyelitis Optica (NMO) and Multiple Sclerosis (MS). Understanding the complex neural path...
A novel SPAST gene splicing variant (c.1617-2A>C) in a heterozygous carrier with hereditary spastic paraplegia [0.03%]
SPAST基因新型突变(c.1617-2A>C)的遗传性痉挛性截瘫杂合子携带者一例
Elvira Sbragia,Andrea Assini,Silvia Calzavara et al.
Elvira Sbragia et al.
Hereditary spastic paraplegia (HSP) is a group of genetically heterogenous neurodegenerative disorders characterized by progressive spasticity and weakness of lower limbs. We report a novel splicing variant (c.1617-2A>C) of the SPAST gene i...
Case Reports
eNeurologicalSci. 2024 May 29:35:100506. DOI:10.1016/j.ensci.2024.100506 2024
Spinal melanoma with optic neuropathy -rare manifestation of Neurocutaneous melanosis and PET-MRI findings [0.03%]
脊柱黑色素瘤伴视神经病变-神经皮肤黑色素病的罕见表现及PET-MRI影像学特征分析
Dipti Baskar,Seena Vengalil,Priyanka Chakkera et al.
Dipti Baskar et al.
Neurocutaneous melanocytosis (NCM) is a rare, sporadic neuroectodermal dysplasia characterized by the presence of large or multiple congenital cutaneous nevi and melanocytic deposits in the central nervous system. Hitherto, unreported we de...
Case Reports
eNeurologicalSci. 2024 May 14:35:100504. DOI:10.1016/j.ensci.2024.100504 2024