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Hopkins syndrome following the first episode of bronchial asthma associated with enterovirus D68: a case report
BACKGROUND: Hopkins syndrome (HS) is a rare disorder presenting with acute flaccid paralysis of the limbs following an asthma attack. Neurologists encounter a diagnostic challenge if patients without a history of bronchial asthma develop neurologic features mimicking HS following acute respiratory d...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5966892/ https://www.ncbi.nlm.nih.gov/pubmed/29792179 http://dx.doi.org/10.1186/s12883-018-1075-7 |
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author | Hayashi, Fumie Hayashi, Shintaro Matsuse, Dai Yamasaki, Ryo Yonekura, Keiji Kira, Jun-ichi |
author_facet | Hayashi, Fumie Hayashi, Shintaro Matsuse, Dai Yamasaki, Ryo Yonekura, Keiji Kira, Jun-ichi |
author_sort | Hayashi, Fumie |
collection | PubMed |
description | BACKGROUND: Hopkins syndrome (HS) is a rare disorder presenting with acute flaccid paralysis of the limbs following an asthma attack. Neurologists encounter a diagnostic challenge if patients without a history of bronchial asthma develop neurologic features mimicking HS following acute respiratory distress. We report a case of HS occurring after a first episode of bronchial asthma associated with enterovirus D68 infection. CASE PRESENTATION: A 5-year-old girl developed acute respiratory distress. On the fourth hospital day, both her legs became paralyzed except for slight muscle contraction in the right lower limb. Tendon reflexes in the lower limbs were diminished and there was a positive Babinski sign on the right. Sensation was normal in all modalities, and there was no uro-rectal disturbance. Spinal magnetic resonance imaging identified T2-hyperintense lesions with spinal cord edema, mainly involving the bilateral T11 to L1 anterior horns, with left side dominance extending to the left posterior horn. The neurological and neuro-radiological findings of our case were suggestive of HS; however, she had no history of bronchial asthma. An acetylcholine inhalation challenge eventually proved the presence of reversible airway hyper-responsiveness, allowing us to diagnose HS. We identified enterovirus D68 in the patient’s intratracheal aspirates using a sensitive polymerase chain reaction assay. Intravenous immunoglobulin administrations at 2 g/kg(2) for 5 consecutive days were repeated every month up to four times. After these treatments, the muscle strength of her right lower limb slightly improved while her left lower leg remained completely paralyzed. CONCLUSION: This case emphasizes the importance of provocation tests to reveal the presence of airway hyper-responsiveness when a child shows neurological signs mimicking HS following acute respiratory distress. Furthermore, the present case suggests a possible link between HS and acute flaccid paralysis following lower respiratory tract infection by enterovirus D68. |
format | Online Article Text |
id | pubmed-5966892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59668922018-05-24 Hopkins syndrome following the first episode of bronchial asthma associated with enterovirus D68: a case report Hayashi, Fumie Hayashi, Shintaro Matsuse, Dai Yamasaki, Ryo Yonekura, Keiji Kira, Jun-ichi BMC Neurol Case Report BACKGROUND: Hopkins syndrome (HS) is a rare disorder presenting with acute flaccid paralysis of the limbs following an asthma attack. Neurologists encounter a diagnostic challenge if patients without a history of bronchial asthma develop neurologic features mimicking HS following acute respiratory distress. We report a case of HS occurring after a first episode of bronchial asthma associated with enterovirus D68 infection. CASE PRESENTATION: A 5-year-old girl developed acute respiratory distress. On the fourth hospital day, both her legs became paralyzed except for slight muscle contraction in the right lower limb. Tendon reflexes in the lower limbs were diminished and there was a positive Babinski sign on the right. Sensation was normal in all modalities, and there was no uro-rectal disturbance. Spinal magnetic resonance imaging identified T2-hyperintense lesions with spinal cord edema, mainly involving the bilateral T11 to L1 anterior horns, with left side dominance extending to the left posterior horn. The neurological and neuro-radiological findings of our case were suggestive of HS; however, she had no history of bronchial asthma. An acetylcholine inhalation challenge eventually proved the presence of reversible airway hyper-responsiveness, allowing us to diagnose HS. We identified enterovirus D68 in the patient’s intratracheal aspirates using a sensitive polymerase chain reaction assay. Intravenous immunoglobulin administrations at 2 g/kg(2) for 5 consecutive days were repeated every month up to four times. After these treatments, the muscle strength of her right lower limb slightly improved while her left lower leg remained completely paralyzed. CONCLUSION: This case emphasizes the importance of provocation tests to reveal the presence of airway hyper-responsiveness when a child shows neurological signs mimicking HS following acute respiratory distress. Furthermore, the present case suggests a possible link between HS and acute flaccid paralysis following lower respiratory tract infection by enterovirus D68. BioMed Central 2018-05-23 /pmc/articles/PMC5966892/ /pubmed/29792179 http://dx.doi.org/10.1186/s12883-018-1075-7 Text en © The Author(s). 2018 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 | Case Report Hayashi, Fumie Hayashi, Shintaro Matsuse, Dai Yamasaki, Ryo Yonekura, Keiji Kira, Jun-ichi Hopkins syndrome following the first episode of bronchial asthma associated with enterovirus D68: a case report |
title | Hopkins syndrome following the first episode of bronchial asthma associated with enterovirus D68: a case report |
title_full | Hopkins syndrome following the first episode of bronchial asthma associated with enterovirus D68: a case report |
title_fullStr | Hopkins syndrome following the first episode of bronchial asthma associated with enterovirus D68: a case report |
title_full_unstemmed | Hopkins syndrome following the first episode of bronchial asthma associated with enterovirus D68: a case report |
title_short | Hopkins syndrome following the first episode of bronchial asthma associated with enterovirus D68: a case report |
title_sort | hopkins syndrome following the first episode of bronchial asthma associated with enterovirus d68: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5966892/ https://www.ncbi.nlm.nih.gov/pubmed/29792179 http://dx.doi.org/10.1186/s12883-018-1075-7 |
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