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Paroxysmal sympathetic hyperactivity syndrome in tuberculous meningitis with paradoxical reaction
INTRODUCTION AND IMPORTANCE: Paroxysmal sympathetic hyperactivity syndrome is frequently reported in traumatic brain injury. However, it may occur in non-traumatic brain injury, such as tuberculous meningitis with hydrocephalus. CASE PRESENTATION: We reported a 38-year-old male who presented with ac...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9568713/ https://www.ncbi.nlm.nih.gov/pubmed/36096085 http://dx.doi.org/10.1016/j.ijscr.2022.107619 |
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author | Siahaan, Andre Marolop Pangihutan Tandean, Steven Indharty, Rr Suzy Nainggolan, Bahagia Willibrodus Maria Susanto, Martin |
author_facet | Siahaan, Andre Marolop Pangihutan Tandean, Steven Indharty, Rr Suzy Nainggolan, Bahagia Willibrodus Maria Susanto, Martin |
author_sort | Siahaan, Andre Marolop Pangihutan |
collection | PubMed |
description | INTRODUCTION AND IMPORTANCE: Paroxysmal sympathetic hyperactivity syndrome is frequently reported in traumatic brain injury. However, it may occur in non-traumatic brain injury, such as tuberculous meningitis with hydrocephalus. CASE PRESENTATION: We reported a 38-year-old male who presented with acute decrease of consciousness and hemiparesis that was developed during antitubercular drugs therapy. CT Scan showed hydrocephalus and granuloma lesion. Emergency ventriculoperitoneal shunting were performed. During treatment, the patient developed paroxysmal sympathetic syndrome during treatment that was controlled based on symptom elimination and prevention. CLINICAL DISCUSSION: Brain tuberculosis remains a difficult problem for clinicians. Even when antitubercular drugs are administered according to protocol, paradoxical reactions can occur. If hydrocephalus develops, ventriculoperitoneal shunting is one of the options for lowering intracranial pressure. Paroxysmal sympathetic hyperactivity may occur in brain tuberculosis and should be detected as soon as possible to avoid serious morbidity. CONCLUSION: Paroxysmal sympathetic hyperactivity may be developed in brain tuberculosis. Early identification and treatment are mandatory. |
format | Online Article Text |
id | pubmed-9568713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-95687132022-10-16 Paroxysmal sympathetic hyperactivity syndrome in tuberculous meningitis with paradoxical reaction Siahaan, Andre Marolop Pangihutan Tandean, Steven Indharty, Rr Suzy Nainggolan, Bahagia Willibrodus Maria Susanto, Martin Int J Surg Case Rep Case Report INTRODUCTION AND IMPORTANCE: Paroxysmal sympathetic hyperactivity syndrome is frequently reported in traumatic brain injury. However, it may occur in non-traumatic brain injury, such as tuberculous meningitis with hydrocephalus. CASE PRESENTATION: We reported a 38-year-old male who presented with acute decrease of consciousness and hemiparesis that was developed during antitubercular drugs therapy. CT Scan showed hydrocephalus and granuloma lesion. Emergency ventriculoperitoneal shunting were performed. During treatment, the patient developed paroxysmal sympathetic syndrome during treatment that was controlled based on symptom elimination and prevention. CLINICAL DISCUSSION: Brain tuberculosis remains a difficult problem for clinicians. Even when antitubercular drugs are administered according to protocol, paradoxical reactions can occur. If hydrocephalus develops, ventriculoperitoneal shunting is one of the options for lowering intracranial pressure. Paroxysmal sympathetic hyperactivity may occur in brain tuberculosis and should be detected as soon as possible to avoid serious morbidity. CONCLUSION: Paroxysmal sympathetic hyperactivity may be developed in brain tuberculosis. Early identification and treatment are mandatory. Elsevier 2022-09-08 /pmc/articles/PMC9568713/ /pubmed/36096085 http://dx.doi.org/10.1016/j.ijscr.2022.107619 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Siahaan, Andre Marolop Pangihutan Tandean, Steven Indharty, Rr Suzy Nainggolan, Bahagia Willibrodus Maria Susanto, Martin Paroxysmal sympathetic hyperactivity syndrome in tuberculous meningitis with paradoxical reaction |
title | Paroxysmal sympathetic hyperactivity syndrome in tuberculous meningitis with paradoxical reaction |
title_full | Paroxysmal sympathetic hyperactivity syndrome in tuberculous meningitis with paradoxical reaction |
title_fullStr | Paroxysmal sympathetic hyperactivity syndrome in tuberculous meningitis with paradoxical reaction |
title_full_unstemmed | Paroxysmal sympathetic hyperactivity syndrome in tuberculous meningitis with paradoxical reaction |
title_short | Paroxysmal sympathetic hyperactivity syndrome in tuberculous meningitis with paradoxical reaction |
title_sort | paroxysmal sympathetic hyperactivity syndrome in tuberculous meningitis with paradoxical reaction |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9568713/ https://www.ncbi.nlm.nih.gov/pubmed/36096085 http://dx.doi.org/10.1016/j.ijscr.2022.107619 |
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