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Stiff-person syndrome coexisting with critical illness polyneuropathy: A case report

RATIONALE: Stiff-person syndrome (SPS) is an uncommon neurological disorder with autoimmune features. Here, we report a 60-year-old man with SPS associated with critical illness polyneuropathy (CIP). CIP was diagnosed during an episode of acute respiratory failure secondary to muscular rigidity and...

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Autores principales: Cai, Qiong, Wu, Chao, Xu, Wenxiao, Liang, Yinxing, Liao, Songjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7738057/
https://www.ncbi.nlm.nih.gov/pubmed/33327330
http://dx.doi.org/10.1097/MD.0000000000023607
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author Cai, Qiong
Wu, Chao
Xu, Wenxiao
Liang, Yinxing
Liao, Songjie
author_facet Cai, Qiong
Wu, Chao
Xu, Wenxiao
Liang, Yinxing
Liao, Songjie
author_sort Cai, Qiong
collection PubMed
description RATIONALE: Stiff-person syndrome (SPS) is an uncommon neurological disorder with autoimmune features. Here, we report a 60-year-old man with SPS associated with critical illness polyneuropathy (CIP). CIP was diagnosed during an episode of acute respiratory failure secondary to muscular rigidity and spasms, which has rarely been reported in this condition. The overlapping of CIP and SPS complicated the case. PATIENT CONCERNS: A 60-year-old man presented with gradual onset of cramps, stiffness, and rigidity in his lower limbs 1 year before admission, which eventually led to inability to stand and walk. The persistent nature of his symptoms progressed to frequent acute episodes of dyspnea and he was admitted to intensive care unit (ICU). DIAGNOSIS: SPS had been diagnosed after 2 tests of electromyography (EMG) and the detection of an elevated anti-GAD65 antibody titer. During the first EMG, low or absent compound muscle action potentials (CMAP), and sensory nerve action potentials (SNAP) were shown. Therefore, the diagnosis of SPS coexisting with CIP was made. INTERVENTIONS: Symptomatic treatment was initiated with oral clonazepam (0.5 mg Bid) and baclofen (5 mg Bid). Intravenous immunoglobulin (IVIG) (0.4 g/kg/d) was administered for the patient for 5 days after admission. We observed a significant clinical improvement during the administration period, and the patient became ambulatory. OUTCOMES: On follow-up, the patient reported complete relief of his pain and rigidity. LESSONS: We report this special case to address the varied clinical features of SPS. Electrophysiological testing is an important diagnostic approach. Accurate recognition of the disease ensures that the patients can be given appropriate treatment without delay.
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spelling pubmed-77380572020-12-16 Stiff-person syndrome coexisting with critical illness polyneuropathy: A case report Cai, Qiong Wu, Chao Xu, Wenxiao Liang, Yinxing Liao, Songjie Medicine (Baltimore) 5300 RATIONALE: Stiff-person syndrome (SPS) is an uncommon neurological disorder with autoimmune features. Here, we report a 60-year-old man with SPS associated with critical illness polyneuropathy (CIP). CIP was diagnosed during an episode of acute respiratory failure secondary to muscular rigidity and spasms, which has rarely been reported in this condition. The overlapping of CIP and SPS complicated the case. PATIENT CONCERNS: A 60-year-old man presented with gradual onset of cramps, stiffness, and rigidity in his lower limbs 1 year before admission, which eventually led to inability to stand and walk. The persistent nature of his symptoms progressed to frequent acute episodes of dyspnea and he was admitted to intensive care unit (ICU). DIAGNOSIS: SPS had been diagnosed after 2 tests of electromyography (EMG) and the detection of an elevated anti-GAD65 antibody titer. During the first EMG, low or absent compound muscle action potentials (CMAP), and sensory nerve action potentials (SNAP) were shown. Therefore, the diagnosis of SPS coexisting with CIP was made. INTERVENTIONS: Symptomatic treatment was initiated with oral clonazepam (0.5 mg Bid) and baclofen (5 mg Bid). Intravenous immunoglobulin (IVIG) (0.4 g/kg/d) was administered for the patient for 5 days after admission. We observed a significant clinical improvement during the administration period, and the patient became ambulatory. OUTCOMES: On follow-up, the patient reported complete relief of his pain and rigidity. LESSONS: We report this special case to address the varied clinical features of SPS. Electrophysiological testing is an important diagnostic approach. Accurate recognition of the disease ensures that the patients can be given appropriate treatment without delay. Lippincott Williams & Wilkins 2020-12-11 /pmc/articles/PMC7738057/ /pubmed/33327330 http://dx.doi.org/10.1097/MD.0000000000023607 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 5300
Cai, Qiong
Wu, Chao
Xu, Wenxiao
Liang, Yinxing
Liao, Songjie
Stiff-person syndrome coexisting with critical illness polyneuropathy: A case report
title Stiff-person syndrome coexisting with critical illness polyneuropathy: A case report
title_full Stiff-person syndrome coexisting with critical illness polyneuropathy: A case report
title_fullStr Stiff-person syndrome coexisting with critical illness polyneuropathy: A case report
title_full_unstemmed Stiff-person syndrome coexisting with critical illness polyneuropathy: A case report
title_short Stiff-person syndrome coexisting with critical illness polyneuropathy: A case report
title_sort stiff-person syndrome coexisting with critical illness polyneuropathy: a case report
topic 5300
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7738057/
https://www.ncbi.nlm.nih.gov/pubmed/33327330
http://dx.doi.org/10.1097/MD.0000000000023607
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