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Reversible splenial lesion syndrome (RESLES) coinciding with cerebral venous thrombosis: a report of two cases

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机构： [a]Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China [b]Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, No.6 Tiantan Xili, Dongcheng District, Beijing, 100050, China

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关键词： cerebral venous thrombosis MRI RESLES splenium corpus callosum

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A total of two postpartum women with no noteworthy medical history presented with persistent headache. Brain magnetic resonance imaging (MRI) of both revealed extensive cerebral venous thrombosis, concurrently with abnormal signals of the splenium of the corpus callosum (SCC): The splenium appeared hyperintense on T2-weighted sequences, fluid-attenuated inversion recovery (FLAIR), and diffusion-weighted imaging (DWI) imaging, and hypointense on T1 sequences and apparent diffusion coefficient (ADC) map. The patients were given thrombolytic therapy. Clinically, both patients achieved recovery with no neurologic sequelae, and follow-up MRI revealed complete resolution of the lesion in the SCC at day 36 and day 37 after initial presentation, respectively. © 2017, © The Author(s), 2017.

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Liu Jingyi Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China Liu Dacheng Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China Yang Bo Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China Yan Jing Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China Pu Yuehua Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China Zhang Jing Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China Wen Miao Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China Yang Zhonghua Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China Liu Liping Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, No.6 Tiantan Xili, Dongcheng District, Beijing, 100050, China [email protected] 12 2017 10 12 375 379 30 3 2017 30 6 2017 © The Author(s), 2017 2017 SAGE Publications Ltd unless otherwise noted. Manuscript content on this site is licensed under Creative Commons Licenses This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License ( http://www.creativecommons.org/licenses/by-nc/4.0/ ) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages ( https://us.sagepub.com/en-us/nam/open-access-at-sage ). A total of two postpartum women with no noteworthy medical history presented with persistent headache. Brain magnetic resonance imaging (MRI) of both revealed extensive cerebral venous thrombosis, concurrently with abnormal signals of the splenium of the corpus callosum (SCC): The splenium appeared hyperintense on T2-weighted sequences, fluid-attenuated inversion recovery (FLAIR), and diffusion-weighted imaging (DWI) imaging, and hypointense on T1 sequences and apparent diffusion coefficient (ADC) map. The patients were given thrombolytic therapy. Clinically, both patients achieved recovery with no neurologic sequelae, and follow-up MRI revealed complete resolution of the lesion in the SCC at day 36 and day 37 after initial presentation, respectively. cerebral venous thrombosis MRI RESLES splenium corpus callosum Funding This work was supported in part by the National Natural Science Foundation of China (#81501004), and by grant No. Z161100004916104 from the Beijing Municipal Science & Technology Commission. Conflict of interest statement The authors declare that there is no conflict of interest.

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出版当年[2016]版中科院分区表Review为是的期刊

：

大类 | 3 区医学

小类 | 3 区临床神经病学

最新[2025]版：

大类 | 2 区医学

小类 | 2 区临床神经病学

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Reversible splenial lesion syndrome (RESLES) coinciding with cerebral venous thrombosis: a report of two cases

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