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Putative pathophysiological mechanisms in recurrent hemicrania from aortic dissection: a case report

BACKGROUND: Transient or permanent neurological symptoms occur in 17–40% of patients with aortic dissection. They can distract from or even mask the underlying life-threatening condition. CASE PRESENTATION: We present the case of a young Caucasian man who consulted for recurrent episodes of stereoty...

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Autores principales: Kamtchum Tatuene, Joseph, Excoffier, Sophie, Vallee, Jean-Paul, Kleinschmidt, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4470358/
https://www.ncbi.nlm.nih.gov/pubmed/26082134
http://dx.doi.org/10.1186/s13104-015-1223-8
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author Kamtchum Tatuene, Joseph
Excoffier, Sophie
Vallee, Jean-Paul
Kleinschmidt, Andreas
author_facet Kamtchum Tatuene, Joseph
Excoffier, Sophie
Vallee, Jean-Paul
Kleinschmidt, Andreas
author_sort Kamtchum Tatuene, Joseph
collection PubMed
description BACKGROUND: Transient or permanent neurological symptoms occur in 17–40% of patients with aortic dissection. They can distract from or even mask the underlying life-threatening condition. CASE PRESENTATION: We present the case of a young Caucasian man who consulted for recurrent episodes of stereotyped right-sided sudden-onset severe headache. Upon questioning, he also reported a dull chest pain. Clinical examination and brain magnetic resonance imaging were unremarkable. The concomitant presence of chest pain made us consider aortic dissection. Contrast-enhanced cervico-thoraco-abdominal computerized tomography revealed type A aortic dissection. The patient underwent surgical replacement of the ascending aorta and reported no further episode of headache thereafter. Differential diagnosis of headache in this case includes paroxysmal hemicrania, cluster headache, migraine, trigeminal neuralgia and short lasting unilateral neuralgiform headache with conjunctival injection and tearing. Failure to match diagnostic criteria for any of these primary headache disorders and the resolution of pain episodes following surgery led us to postulate that these new-onset hemicrania episodes were symptomatic of aortic dissection. We hypothesize that aortic wall ischemia could have activated the trigeminovascular system and thereby caused hemicranial pain. Such an effect might be mediated by two different pathways that can be referred to as anatomical and humoral. The humoral hypothesis would posit that ischemia results in synthesis of pro-inflammatory mediators released from the aortic wall into the blood stream, such that they reach the central nervous system and directly stimulate specific receptors. The anatomical hypothesis would imply that pain signals generated by nociceptors in the aortic wall are transferred to the trigeminal ganglion via the cardiac plexus, the first cervical ganglion and the internal carotid nerve such that pain perception is referred to related cranio-cervical dermatomes. CONCLUSION: In cases of isolated headache that does not match key diagnostic criteria for a primary headache entity; a thorough review of systems should be performed to look for symptoms that may indicate symptomatic headache from potentially life-threatening conditions. Neurologists should consider aortic dissection in patients presenting with acute headache and chest pain. Further clinical or experimental studies are required to refute or validate the pathophysiological hypothesis discussed here.
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spelling pubmed-44703582015-06-18 Putative pathophysiological mechanisms in recurrent hemicrania from aortic dissection: a case report Kamtchum Tatuene, Joseph Excoffier, Sophie Vallee, Jean-Paul Kleinschmidt, Andreas BMC Res Notes Case Report BACKGROUND: Transient or permanent neurological symptoms occur in 17–40% of patients with aortic dissection. They can distract from or even mask the underlying life-threatening condition. CASE PRESENTATION: We present the case of a young Caucasian man who consulted for recurrent episodes of stereotyped right-sided sudden-onset severe headache. Upon questioning, he also reported a dull chest pain. Clinical examination and brain magnetic resonance imaging were unremarkable. The concomitant presence of chest pain made us consider aortic dissection. Contrast-enhanced cervico-thoraco-abdominal computerized tomography revealed type A aortic dissection. The patient underwent surgical replacement of the ascending aorta and reported no further episode of headache thereafter. Differential diagnosis of headache in this case includes paroxysmal hemicrania, cluster headache, migraine, trigeminal neuralgia and short lasting unilateral neuralgiform headache with conjunctival injection and tearing. Failure to match diagnostic criteria for any of these primary headache disorders and the resolution of pain episodes following surgery led us to postulate that these new-onset hemicrania episodes were symptomatic of aortic dissection. We hypothesize that aortic wall ischemia could have activated the trigeminovascular system and thereby caused hemicranial pain. Such an effect might be mediated by two different pathways that can be referred to as anatomical and humoral. The humoral hypothesis would posit that ischemia results in synthesis of pro-inflammatory mediators released from the aortic wall into the blood stream, such that they reach the central nervous system and directly stimulate specific receptors. The anatomical hypothesis would imply that pain signals generated by nociceptors in the aortic wall are transferred to the trigeminal ganglion via the cardiac plexus, the first cervical ganglion and the internal carotid nerve such that pain perception is referred to related cranio-cervical dermatomes. CONCLUSION: In cases of isolated headache that does not match key diagnostic criteria for a primary headache entity; a thorough review of systems should be performed to look for symptoms that may indicate symptomatic headache from potentially life-threatening conditions. Neurologists should consider aortic dissection in patients presenting with acute headache and chest pain. Further clinical or experimental studies are required to refute or validate the pathophysiological hypothesis discussed here. BioMed Central 2015-06-17 /pmc/articles/PMC4470358/ /pubmed/26082134 http://dx.doi.org/10.1186/s13104-015-1223-8 Text en © Kamtchum Tatuene et al. 2015 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
Kamtchum Tatuene, Joseph
Excoffier, Sophie
Vallee, Jean-Paul
Kleinschmidt, Andreas
Putative pathophysiological mechanisms in recurrent hemicrania from aortic dissection: a case report
title Putative pathophysiological mechanisms in recurrent hemicrania from aortic dissection: a case report
title_full Putative pathophysiological mechanisms in recurrent hemicrania from aortic dissection: a case report
title_fullStr Putative pathophysiological mechanisms in recurrent hemicrania from aortic dissection: a case report
title_full_unstemmed Putative pathophysiological mechanisms in recurrent hemicrania from aortic dissection: a case report
title_short Putative pathophysiological mechanisms in recurrent hemicrania from aortic dissection: a case report
title_sort putative pathophysiological mechanisms in recurrent hemicrania from aortic dissection: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4470358/
https://www.ncbi.nlm.nih.gov/pubmed/26082134
http://dx.doi.org/10.1186/s13104-015-1223-8
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