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Paroxysmal Sympathetic Hyperactivity in a 73-Year-Old Female With Acute Myeloid Leukemia

Paroxysmal Sympathetic Hyperactivity (PSH) is a syndrome of recurrent exaggerated sympathetic responses in combination with motor features typically observed in the setting of traumatic brain injury and rarely seen without it. Here, we present a case of PSH in a 73-year-old female with acute myeloid...

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Autores principales: Lokineni, Sravani, Tirthani, Ekta, Wuest, Julia, Ayyad, Rania
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351252/
https://www.ncbi.nlm.nih.gov/pubmed/34381652
http://dx.doi.org/10.7759/cureus.16293
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author Lokineni, Sravani
Tirthani, Ekta
Wuest, Julia
Ayyad, Rania
author_facet Lokineni, Sravani
Tirthani, Ekta
Wuest, Julia
Ayyad, Rania
author_sort Lokineni, Sravani
collection PubMed
description Paroxysmal Sympathetic Hyperactivity (PSH) is a syndrome of recurrent exaggerated sympathetic responses in combination with motor features typically observed in the setting of traumatic brain injury and rarely seen without it. Here, we present a case of PSH in a 73-year-old female with acute myeloid leukemia (AML) without any brain injuries presenting with recurrent intermittent episodes of tachycardia, tachypnea, hypertension, fever, dystonia. These episodes resolved with clonidine and clonazepam thus confirming the diagnosis of PSH. PSH is an unusual and rare presentation in AML and not much literature has been reported.
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spelling pubmed-83512522021-08-10 Paroxysmal Sympathetic Hyperactivity in a 73-Year-Old Female With Acute Myeloid Leukemia Lokineni, Sravani Tirthani, Ekta Wuest, Julia Ayyad, Rania Cureus Neurology Paroxysmal Sympathetic Hyperactivity (PSH) is a syndrome of recurrent exaggerated sympathetic responses in combination with motor features typically observed in the setting of traumatic brain injury and rarely seen without it. Here, we present a case of PSH in a 73-year-old female with acute myeloid leukemia (AML) without any brain injuries presenting with recurrent intermittent episodes of tachycardia, tachypnea, hypertension, fever, dystonia. These episodes resolved with clonidine and clonazepam thus confirming the diagnosis of PSH. PSH is an unusual and rare presentation in AML and not much literature has been reported. Cureus 2021-07-10 /pmc/articles/PMC8351252/ /pubmed/34381652 http://dx.doi.org/10.7759/cureus.16293 Text en Copyright © 2021, Lokineni et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Neurology
Lokineni, Sravani
Tirthani, Ekta
Wuest, Julia
Ayyad, Rania
Paroxysmal Sympathetic Hyperactivity in a 73-Year-Old Female With Acute Myeloid Leukemia
title Paroxysmal Sympathetic Hyperactivity in a 73-Year-Old Female With Acute Myeloid Leukemia
title_full Paroxysmal Sympathetic Hyperactivity in a 73-Year-Old Female With Acute Myeloid Leukemia
title_fullStr Paroxysmal Sympathetic Hyperactivity in a 73-Year-Old Female With Acute Myeloid Leukemia
title_full_unstemmed Paroxysmal Sympathetic Hyperactivity in a 73-Year-Old Female With Acute Myeloid Leukemia
title_short Paroxysmal Sympathetic Hyperactivity in a 73-Year-Old Female With Acute Myeloid Leukemia
title_sort paroxysmal sympathetic hyperactivity in a 73-year-old female with acute myeloid leukemia
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351252/
https://www.ncbi.nlm.nih.gov/pubmed/34381652
http://dx.doi.org/10.7759/cureus.16293
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