Clinical and Magnetic Resonance Imaging Features of Reversible Splenial Lesion Syndrome in Adults: A Small Case Series

被引:4
作者
Xu, Wen [1 ]
Zhou, Yan [2 ]
Jiang, Yan [1 ]
Zhang, Li [1 ]
Tang, Qiqiang [1 ]
机构
[1] Univ Sci & Technol China, Div Life Sci & Med, Affiliated Hosp 1, Dept Neurol, Hefei 230001, Anhui, Peoples R China
[2] Affiliated Anhui Med Univ, Anhui Prov Childrens Hosp, Dept Childrens Hlth Prevent, Hefei, Peoples R China
基金
中国国家自然科学基金;
关键词
Reversible splenial lesion syndrome; Clinical manifestation; Splenium of corpus callosum; Cerebrospinal fluid; Magnetic resonance imaging; CORPUS-CALLOSUM; MILD ENCEPHALITIS/ENCEPHALOPATHY;
D O I
10.1159/000505019
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: To study clinical and magnetic resonance imaging (MRI) features of reversible splenial lesion syndrome (RESLES) in adult patients. Methods: A retrospective analysis was performed using clinical, cerebrospinal fluid (CSF), laboratory results, and neuroimaging data obtained from 6 adult RESLES patients. Results: All 6 patients (3 male cases, 3 female cases) were determined to be acute or subacute onset, most of them associated with infection or fever. All initial MRI data exhibited splenium of corpus callosum lesions with hypointensity on T1WI, hyperintensity on T2WI, diffusion-weighted imaging (DWI) and Flair, without significant gadolinium enhancement. Five patients were treated with glucocorticoids and showed significant improvement in 1-15 days, with the lesion having disappeared or weakened, and one case was lost of follow-up. The cell number and protein amount in CSF were determined to be at normal levels, or slightly increased in 3 patients with thyroid dysfunction. Conclusion: The etiology of adult RESLES was observed to be complex and diverse, primarily related to infection, fever, and thyroid dysfunction. DWI was found to be more sensitive in these lesions, and CSF cytology was observed to be either normal or mildly abnormal. A majority of patients were found to be sensitive to glucocorticoid, and have a good prognosis with lesions that disappeared rapidly.
引用
收藏
页码:86 / 92
页数:7
相关论文
共 26 条
[11]  
Kitami M, 2011, J MED CASE REPORTS, V5, P54
[12]  
Kurokawa Yoshie, 2017, Nihon Rinsho Meneki Gakkai Kaishi, V40, P190, DOI 10.2177/jsci.40.190
[13]   Reversible splenial lesion syndrome associated with lobar pneumonia: Case report and review of literature [J].
Li, Chunrong ;
Wu, Xiujuan ;
Qi, Hehe ;
Cheng, Yanwei ;
Zhang, Bing ;
Zhou, Hongwei ;
Lv, Xiaohong ;
Liu, Kangding ;
Zhang, Hong-Liang .
MEDICINE, 2016, 95 (39)
[14]   Reversible splenial lesion in the corpus callosum following rapid withdrawal of carbamazepine after neurosurgical decompression for trigeminal neuralgia [J].
Mori, Harushi ;
Maeda, Masayuki ;
Takanashi, Jun-ichi ;
Kunimatsu, Akira ;
Matsushima, Nobuyoshi ;
Suzuki, Hidenori ;
Saito, Nobuhito ;
Ohtomo, Kuni .
JOURNAL OF CLINICAL NEUROSCIENCE, 2012, 19 (08) :1182-1184
[15]   A thyroid storm patient with protracted disturbance of consciousness and reversible lesion in the splenium of corpus callosum A case report [J].
Namatame, Chihiro ;
Sonoo, Tomohiro ;
Fukushima, Kazutaka ;
Naraba, Hiromu ;
Hashimoto, Hideki ;
Nakamura, Kensuke .
MEDICINE, 2018, 97 (07)
[16]   An MRI review of acquired corpus callosum lesions [J].
Renard, Dimitri ;
Castelnovo, Giovanni ;
Campello, Chantal ;
Bouly, Stephane ;
Le Floch, Anne ;
Thouvenot, Eric ;
Waconge, Anne ;
Taieb, Guillaume .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2014, 85 (09) :1041-1048
[17]   Kawasaki disease-associated MERS: Pathological insights from SPECT findings [J].
Sato, Tatsuharu ;
Ushiroda, Yoko ;
Oyama, Toshifumi ;
Nakatomi, Akiko ;
Motomura, Hideki ;
Moriuchi, Hiroyuki .
BRAIN & DEVELOPMENT, 2012, 34 (07) :605-608
[18]   Neuropsychological Profile of Agenesis of the Corpus Callosum: A Systematic Review [J].
Siffredi, Vanessa ;
Anderson, Vicki ;
Leventer, Richard J. ;
Spencer-Smith, Megan M. .
DEVELOPMENTAL NEUROPSYCHOLOGY, 2013, 38 (01) :36-57
[19]   Clinically mild encephalitis/encephalopathy with a reversible splenial lesion [J].
Tada, H ;
Takanashi, J ;
Barkovich, AJ ;
Oba, H ;
Maeda, M ;
Tsukahara, H ;
Suzuki, M ;
Yamamoto, T ;
Shimono, T ;
Ichiyama, T ;
Taoka, T ;
Sohma, O ;
Yoshikawa, H ;
Kohno, Y .
NEUROLOGY, 2004, 63 (10) :1854-1858
[20]  
Takanashi J, 2006, AM J NEURORADIOL, V27, P836