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Orbital phlebography in idiopathic intracranial hypertension and chronic tension-type headache

BACKGROUND: Pathologic signs in orbital phlebographies have been reported in various neurological diseases. PURPOSE: To study if pathologic signs in orbital phlebography may be markers of inflammation primarily affecting intracranial capillaries, which would cause intracranial hypertension. MATERIAL...

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Autores principales: Hannerz, Jan, Ericson, Kaj, Greitz, Dan, Skejo, Pernille Hanne Bro, Edman, Gunnar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3859250/
https://www.ncbi.nlm.nih.gov/pubmed/24349708
http://dx.doi.org/10.1177/2047981613498861
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author Hannerz, Jan
Ericson, Kaj
Greitz, Dan
Skejo, Pernille Hanne Bro
Edman, Gunnar
author_facet Hannerz, Jan
Ericson, Kaj
Greitz, Dan
Skejo, Pernille Hanne Bro
Edman, Gunnar
author_sort Hannerz, Jan
collection PubMed
description BACKGROUND: Pathologic signs in orbital phlebographies have been reported in various neurological diseases. PURPOSE: To study if pathologic signs in orbital phlebography may be markers of inflammation primarily affecting intracranial capillaries, which would cause intracranial hypertension. MATERIAL AND METHODS: Two groups with different intracranial cerebrospinal fluid pressures (Pcsf) were compared as to inflammatory markers in serum and pathologic signs in orbital phlebographies. Nine consecutive patients with idiopathic intracranial hypertension (IIH) with bilateral papilledema and eight consecutive patients with chronic tension-type headache (CTTH) were investigated prospectively with fibrinogen, orosomucoid, haptoglobin in serum, and invasive orbital phlebograms. The angiograms were evaluated by two skilled neuroradiologists, independent of each other and without knowledge of the diagnoses or aim of the study, as to the following pathologic signs: (i) narrowing of superior ophthalmic veins; (ii) caliber changes of intraorbital veins; (iii) collaterals of intraorbital veins; (iv) flow to cavernous sinus; and (v) asymmetric drainage of cavernous sinus. RESULTS: Mean body mass index was >30 kg/m(2) in both groups. Pcsf was >200 < 250 mm H(2)O in 50% of the CTTH and >350 mm H(2)O in all IIH patients. No difference in inflammatory markers in blood was found. The phlebographies of the IIH patients had more pathologic signs and were considered pathologic significantly more often than the ones of the CTTH patients (P < 0.001). CONCLUSION: The difference as to phlebographic pathologic signs between the IIH and the CTTH patients with different Pcsf supports the hypothesis that such phlebographic signs are markers of inflammation primarily affecting intracranial capillaries, which would disturb cerebrospinal fluid regulation causing intracranial hypertension.
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spelling pubmed-38592502013-12-13 Orbital phlebography in idiopathic intracranial hypertension and chronic tension-type headache Hannerz, Jan Ericson, Kaj Greitz, Dan Skejo, Pernille Hanne Bro Edman, Gunnar Acta Radiol Short Rep Original Article BACKGROUND: Pathologic signs in orbital phlebographies have been reported in various neurological diseases. PURPOSE: To study if pathologic signs in orbital phlebography may be markers of inflammation primarily affecting intracranial capillaries, which would cause intracranial hypertension. MATERIAL AND METHODS: Two groups with different intracranial cerebrospinal fluid pressures (Pcsf) were compared as to inflammatory markers in serum and pathologic signs in orbital phlebographies. Nine consecutive patients with idiopathic intracranial hypertension (IIH) with bilateral papilledema and eight consecutive patients with chronic tension-type headache (CTTH) were investigated prospectively with fibrinogen, orosomucoid, haptoglobin in serum, and invasive orbital phlebograms. The angiograms were evaluated by two skilled neuroradiologists, independent of each other and without knowledge of the diagnoses or aim of the study, as to the following pathologic signs: (i) narrowing of superior ophthalmic veins; (ii) caliber changes of intraorbital veins; (iii) collaterals of intraorbital veins; (iv) flow to cavernous sinus; and (v) asymmetric drainage of cavernous sinus. RESULTS: Mean body mass index was >30 kg/m(2) in both groups. Pcsf was >200 < 250 mm H(2)O in 50% of the CTTH and >350 mm H(2)O in all IIH patients. No difference in inflammatory markers in blood was found. The phlebographies of the IIH patients had more pathologic signs and were considered pathologic significantly more often than the ones of the CTTH patients (P < 0.001). CONCLUSION: The difference as to phlebographic pathologic signs between the IIH and the CTTH patients with different Pcsf supports the hypothesis that such phlebographic signs are markers of inflammation primarily affecting intracranial capillaries, which would disturb cerebrospinal fluid regulation causing intracranial hypertension. SAGE Publications 2013-10-29 /pmc/articles/PMC3859250/ /pubmed/24349708 http://dx.doi.org/10.1177/2047981613498861 Text en © The Foundation Acta Radiologica 2013 Reprints and permissions: sagepub.co.uk/journalsPermissions.nav
spellingShingle Original Article
Hannerz, Jan
Ericson, Kaj
Greitz, Dan
Skejo, Pernille Hanne Bro
Edman, Gunnar
Orbital phlebography in idiopathic intracranial hypertension and chronic tension-type headache
title Orbital phlebography in idiopathic intracranial hypertension and chronic tension-type headache
title_full Orbital phlebography in idiopathic intracranial hypertension and chronic tension-type headache
title_fullStr Orbital phlebography in idiopathic intracranial hypertension and chronic tension-type headache
title_full_unstemmed Orbital phlebography in idiopathic intracranial hypertension and chronic tension-type headache
title_short Orbital phlebography in idiopathic intracranial hypertension and chronic tension-type headache
title_sort orbital phlebography in idiopathic intracranial hypertension and chronic tension-type headache
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3859250/
https://www.ncbi.nlm.nih.gov/pubmed/24349708
http://dx.doi.org/10.1177/2047981613498861
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