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Pure dysarthria and dysarthria-facial paresis syndrome due to internal capsule and/or corona radiata infarction

BACKGROUND: Pure dysarthria (PD) and dysarthria-facial paresis syndrome (DFP) mainly result from lenticulostriate artery territory infarction. PD and DFP are rare clinical entities, often grouped without distinction. The purpose of this study was to examine clinical and radiographic differences betw...

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Autores principales: Tanaka, Koji, Yamada, Takeshi, Torii, Takako, Yoshimura, Takeo, Takase, Kei-ichiro, Togao, Osamu, Wakata, Yoshifumi, Hiwatashi, Akio, Nakashima, Naoki, Kira, Jun-ichi, Murai, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4597455/
https://www.ncbi.nlm.nih.gov/pubmed/26445963
http://dx.doi.org/10.1186/s12883-015-0439-5
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author Tanaka, Koji
Yamada, Takeshi
Torii, Takako
Yoshimura, Takeo
Takase, Kei-ichiro
Togao, Osamu
Wakata, Yoshifumi
Hiwatashi, Akio
Nakashima, Naoki
Kira, Jun-ichi
Murai, Hiroyuki
author_facet Tanaka, Koji
Yamada, Takeshi
Torii, Takako
Yoshimura, Takeo
Takase, Kei-ichiro
Togao, Osamu
Wakata, Yoshifumi
Hiwatashi, Akio
Nakashima, Naoki
Kira, Jun-ichi
Murai, Hiroyuki
author_sort Tanaka, Koji
collection PubMed
description BACKGROUND: Pure dysarthria (PD) and dysarthria-facial paresis syndrome (DFP) mainly result from lenticulostriate artery territory infarction. PD and DFP are rare clinical entities, often grouped without distinction. The purpose of this study was to examine clinical and radiographic differences between PD and DFP due to unilateral internal capsule and/or corona radiata infarction. METHODS: Using a database that included consecutive patients with ischemic stroke admitted to the neurological stroke units of three hospitals within 7 days from onset between September 2011 and April 2014, we retrospectively extracted first-ever stroke patient data, who presented with PD or DFP with a single ischemic lesion localized in the internal capsule and/or corona radiata. Patients with weakness, ataxia, sensory deficit, or cortical symptoms were excluded. Ischemic lesion volume was calculated by the ABC/2 method on diffusion-weighted imaging (DWI). DWI images were normalized and superimposed to the template for PD and DFP. We compared patients' characteristics between PD and DFP. RESULTS: A total of 2126 patients, including 65 patients (3.1 %) with PD or DFP, were registered. Of these, 13 PD patients and 18 patients with DFP due to unilateral internal capsule and/or corona radiata infarction were included for analysis. Compared with DFP patients, PD patients had longer onset-to-door time (median 37.5 vs. 10.8 h, p = 0.031), shorter vertical length (C component) of ischemic lesions (median 12.0 vs. 18.8 mm, p = 0.007), and smaller ischemic lesion volume (median 285 vs. 828 mm(3), p = 0.023). Ischemic lesions causing PD were located more frequently in the left hemisphere than DFP (92 % vs. 56 %, p = 0.045). The superimposed lesion pattern indicated that DFP had lesions more medial and involving posterior portions of the putamen and the caudate body, as well as more of the genu and posterior limb of the internal capsule, than PD. Ninety days after onset, symptoms disappeared in 21 (72 %) out of 29 patients. CONCLUSIONS: In cerebral infarction limited to the internal capsule and/or corona radiata, PD is derived from smaller and left-sided lesions with delay in diagnosis compared with DFP. The clinical course of those with PD and DFP might be benign.
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spelling pubmed-45974552015-10-09 Pure dysarthria and dysarthria-facial paresis syndrome due to internal capsule and/or corona radiata infarction Tanaka, Koji Yamada, Takeshi Torii, Takako Yoshimura, Takeo Takase, Kei-ichiro Togao, Osamu Wakata, Yoshifumi Hiwatashi, Akio Nakashima, Naoki Kira, Jun-ichi Murai, Hiroyuki BMC Neurol Research Article BACKGROUND: Pure dysarthria (PD) and dysarthria-facial paresis syndrome (DFP) mainly result from lenticulostriate artery territory infarction. PD and DFP are rare clinical entities, often grouped without distinction. The purpose of this study was to examine clinical and radiographic differences between PD and DFP due to unilateral internal capsule and/or corona radiata infarction. METHODS: Using a database that included consecutive patients with ischemic stroke admitted to the neurological stroke units of three hospitals within 7 days from onset between September 2011 and April 2014, we retrospectively extracted first-ever stroke patient data, who presented with PD or DFP with a single ischemic lesion localized in the internal capsule and/or corona radiata. Patients with weakness, ataxia, sensory deficit, or cortical symptoms were excluded. Ischemic lesion volume was calculated by the ABC/2 method on diffusion-weighted imaging (DWI). DWI images were normalized and superimposed to the template for PD and DFP. We compared patients' characteristics between PD and DFP. RESULTS: A total of 2126 patients, including 65 patients (3.1 %) with PD or DFP, were registered. Of these, 13 PD patients and 18 patients with DFP due to unilateral internal capsule and/or corona radiata infarction were included for analysis. Compared with DFP patients, PD patients had longer onset-to-door time (median 37.5 vs. 10.8 h, p = 0.031), shorter vertical length (C component) of ischemic lesions (median 12.0 vs. 18.8 mm, p = 0.007), and smaller ischemic lesion volume (median 285 vs. 828 mm(3), p = 0.023). Ischemic lesions causing PD were located more frequently in the left hemisphere than DFP (92 % vs. 56 %, p = 0.045). The superimposed lesion pattern indicated that DFP had lesions more medial and involving posterior portions of the putamen and the caudate body, as well as more of the genu and posterior limb of the internal capsule, than PD. Ninety days after onset, symptoms disappeared in 21 (72 %) out of 29 patients. CONCLUSIONS: In cerebral infarction limited to the internal capsule and/or corona radiata, PD is derived from smaller and left-sided lesions with delay in diagnosis compared with DFP. The clinical course of those with PD and DFP might be benign. BioMed Central 2015-10-07 /pmc/articles/PMC4597455/ /pubmed/26445963 http://dx.doi.org/10.1186/s12883-015-0439-5 Text en © Tanaka et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Tanaka, Koji
Yamada, Takeshi
Torii, Takako
Yoshimura, Takeo
Takase, Kei-ichiro
Togao, Osamu
Wakata, Yoshifumi
Hiwatashi, Akio
Nakashima, Naoki
Kira, Jun-ichi
Murai, Hiroyuki
Pure dysarthria and dysarthria-facial paresis syndrome due to internal capsule and/or corona radiata infarction
title Pure dysarthria and dysarthria-facial paresis syndrome due to internal capsule and/or corona radiata infarction
title_full Pure dysarthria and dysarthria-facial paresis syndrome due to internal capsule and/or corona radiata infarction
title_fullStr Pure dysarthria and dysarthria-facial paresis syndrome due to internal capsule and/or corona radiata infarction
title_full_unstemmed Pure dysarthria and dysarthria-facial paresis syndrome due to internal capsule and/or corona radiata infarction
title_short Pure dysarthria and dysarthria-facial paresis syndrome due to internal capsule and/or corona radiata infarction
title_sort pure dysarthria and dysarthria-facial paresis syndrome due to internal capsule and/or corona radiata infarction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4597455/
https://www.ncbi.nlm.nih.gov/pubmed/26445963
http://dx.doi.org/10.1186/s12883-015-0439-5
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