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Paroxysmal autonomic instability with dystonia in a patient with tuberculous meningitis: a case report

INTRODUCTION: This case report describes an extremely rare combination of paroxysmal autonomic instability with dystonia and tuberculous meningitis. Paroxysmal autonomic instability with dystonia is normally associated with severe traumatic brain injury. CASE PRESENTATION: A 69-year-old man of Indon...

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Autores principales: Ramdhani, Navin A, Sikma, Maaike A, Witkamp, Theo D, Slooter, Arjen JC, de Lange, Dylan W
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2944193/
https://www.ncbi.nlm.nih.gov/pubmed/20831807
http://dx.doi.org/10.1186/1752-1947-4-304
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author Ramdhani, Navin A
Sikma, Maaike A
Witkamp, Theo D
Slooter, Arjen JC
de Lange, Dylan W
author_facet Ramdhani, Navin A
Sikma, Maaike A
Witkamp, Theo D
Slooter, Arjen JC
de Lange, Dylan W
author_sort Ramdhani, Navin A
collection PubMed
description INTRODUCTION: This case report describes an extremely rare combination of paroxysmal autonomic instability with dystonia and tuberculous meningitis. Paroxysmal autonomic instability with dystonia is normally associated with severe traumatic brain injury. CASE PRESENTATION: A 69-year-old man of Indonesian descent was initially suspected of having a community-acquired pneumonia, which was seen on chest X-ray and computed tomography of the chest. However, a bronchoscopy showed no abnormalities. He was treated with amoxicillin-clavulanic acid in combination with ciprofloxacin. However, nine days after admission he was disorientated and complained of headache. Neurological examination revealed no further abnormalities. A lumbar puncture revealed no evidence of meningitis. He was then transferred to our hospital. At that time, initial cultures of bronchial fluid for Mycobacterium tuberculosis turned positive, as well as polymerase chain reaction for Mycobacterium tuberculosis. Later, during his stay in our intensive care unit, he developed periods with hypertension, sinus tachycardia, excessive transpiration, decreased oxygen saturation with tachypnea, pink foamy sputum, and high fever. This constellation of symptoms was accompanied by dystonia in the first days. These episodes lasted approximately 30 minutes and improved after administration of morphine, benzodiazepines or clonidine. Magnetic resonance imaging showed an abnormal signal in the region of the hippocampus, thalamus and the anterior parts of the lentiform nucleus and caudate nucleus. CONCLUSIONS: In patients with (tuberculous) meningitis and episodes of extreme hypertension and fever, paroxysmal autonomic instability with dystonia should be considered.
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spelling pubmed-29441932010-09-24 Paroxysmal autonomic instability with dystonia in a patient with tuberculous meningitis: a case report Ramdhani, Navin A Sikma, Maaike A Witkamp, Theo D Slooter, Arjen JC de Lange, Dylan W J Med Case Reports Case Report INTRODUCTION: This case report describes an extremely rare combination of paroxysmal autonomic instability with dystonia and tuberculous meningitis. Paroxysmal autonomic instability with dystonia is normally associated with severe traumatic brain injury. CASE PRESENTATION: A 69-year-old man of Indonesian descent was initially suspected of having a community-acquired pneumonia, which was seen on chest X-ray and computed tomography of the chest. However, a bronchoscopy showed no abnormalities. He was treated with amoxicillin-clavulanic acid in combination with ciprofloxacin. However, nine days after admission he was disorientated and complained of headache. Neurological examination revealed no further abnormalities. A lumbar puncture revealed no evidence of meningitis. He was then transferred to our hospital. At that time, initial cultures of bronchial fluid for Mycobacterium tuberculosis turned positive, as well as polymerase chain reaction for Mycobacterium tuberculosis. Later, during his stay in our intensive care unit, he developed periods with hypertension, sinus tachycardia, excessive transpiration, decreased oxygen saturation with tachypnea, pink foamy sputum, and high fever. This constellation of symptoms was accompanied by dystonia in the first days. These episodes lasted approximately 30 minutes and improved after administration of morphine, benzodiazepines or clonidine. Magnetic resonance imaging showed an abnormal signal in the region of the hippocampus, thalamus and the anterior parts of the lentiform nucleus and caudate nucleus. CONCLUSIONS: In patients with (tuberculous) meningitis and episodes of extreme hypertension and fever, paroxysmal autonomic instability with dystonia should be considered. BioMed Central 2010-09-10 /pmc/articles/PMC2944193/ /pubmed/20831807 http://dx.doi.org/10.1186/1752-1947-4-304 Text en Copyright ©2010 Ramdhani et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ramdhani, Navin A
Sikma, Maaike A
Witkamp, Theo D
Slooter, Arjen JC
de Lange, Dylan W
Paroxysmal autonomic instability with dystonia in a patient with tuberculous meningitis: a case report
title Paroxysmal autonomic instability with dystonia in a patient with tuberculous meningitis: a case report
title_full Paroxysmal autonomic instability with dystonia in a patient with tuberculous meningitis: a case report
title_fullStr Paroxysmal autonomic instability with dystonia in a patient with tuberculous meningitis: a case report
title_full_unstemmed Paroxysmal autonomic instability with dystonia in a patient with tuberculous meningitis: a case report
title_short Paroxysmal autonomic instability with dystonia in a patient with tuberculous meningitis: a case report
title_sort paroxysmal autonomic instability with dystonia in a patient with tuberculous meningitis: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2944193/
https://www.ncbi.nlm.nih.gov/pubmed/20831807
http://dx.doi.org/10.1186/1752-1947-4-304
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