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Reversible cerebral vasoconstriction syndrome: case report

A 28-year-old woman had thunderclap headache (TCH), after 7 days she had left hemiparesis. She had a history of oral contraceptive and citalopram medications. Brain magnetic resonance (MR) angiography demonstrated multiple stenotic segments. Digital subtraction angiography (DSA) showed multiple segm...

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Detalles Bibliográficos
Autores principales: Öz, Oğuzhan, Demirkaya, Şeref, Bek, Semai, Eroğlu, Erdal, Ulaş, Ümit Hıdır, Odabaşı, Zeki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3451746/
https://www.ncbi.nlm.nih.gov/pubmed/19370308
http://dx.doi.org/10.1007/s10194-009-0117-3
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author Öz, Oğuzhan
Demirkaya, Şeref
Bek, Semai
Eroğlu, Erdal
Ulaş, Ümit Hıdır
Odabaşı, Zeki
author_facet Öz, Oğuzhan
Demirkaya, Şeref
Bek, Semai
Eroğlu, Erdal
Ulaş, Ümit Hıdır
Odabaşı, Zeki
author_sort Öz, Oğuzhan
collection PubMed
description A 28-year-old woman had thunderclap headache (TCH), after 7 days she had left hemiparesis. She had a history of oral contraceptive and citalopram medications. Brain magnetic resonance (MR) angiography demonstrated multiple stenotic segments. Digital subtraction angiography (DSA) showed multiple segments of narrowing in vessel calibre. Two probable diagnoses performed; primary angiitis of the central nervous system and reversible cerebral vasoconstriction syndrome (RCVS). Because of clinical characteristics and normal cerebrospinal fluid findings she was set on medication for probable RCVS. Follow-up MR angiography after 4 weeks and DSA after 7 weeks demonstrated improvement in vessel calibre. Thus, diagnosis RCVS was established. Diagnosis and management of TCH contain many potential difficulties. Clinicians should consider the imaging of cerebral arteries, even if computed tomography scan and lumbar puncture are normal in TCH. Potential precipitating factors and triggers should also be known and avoided.
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spelling pubmed-34517462012-11-29 Reversible cerebral vasoconstriction syndrome: case report Öz, Oğuzhan Demirkaya, Şeref Bek, Semai Eroğlu, Erdal Ulaş, Ümit Hıdır Odabaşı, Zeki J Headache Pain Brief Report A 28-year-old woman had thunderclap headache (TCH), after 7 days she had left hemiparesis. She had a history of oral contraceptive and citalopram medications. Brain magnetic resonance (MR) angiography demonstrated multiple stenotic segments. Digital subtraction angiography (DSA) showed multiple segments of narrowing in vessel calibre. Two probable diagnoses performed; primary angiitis of the central nervous system and reversible cerebral vasoconstriction syndrome (RCVS). Because of clinical characteristics and normal cerebrospinal fluid findings she was set on medication for probable RCVS. Follow-up MR angiography after 4 weeks and DSA after 7 weeks demonstrated improvement in vessel calibre. Thus, diagnosis RCVS was established. Diagnosis and management of TCH contain many potential difficulties. Clinicians should consider the imaging of cerebral arteries, even if computed tomography scan and lumbar puncture are normal in TCH. Potential precipitating factors and triggers should also be known and avoided. Springer Milan 2009-04-16 2009-08 /pmc/articles/PMC3451746/ /pubmed/19370308 http://dx.doi.org/10.1007/s10194-009-0117-3 Text en © Springer-Verlag 2009
spellingShingle Brief Report
Öz, Oğuzhan
Demirkaya, Şeref
Bek, Semai
Eroğlu, Erdal
Ulaş, Ümit Hıdır
Odabaşı, Zeki
Reversible cerebral vasoconstriction syndrome: case report
title Reversible cerebral vasoconstriction syndrome: case report
title_full Reversible cerebral vasoconstriction syndrome: case report
title_fullStr Reversible cerebral vasoconstriction syndrome: case report
title_full_unstemmed Reversible cerebral vasoconstriction syndrome: case report
title_short Reversible cerebral vasoconstriction syndrome: case report
title_sort reversible cerebral vasoconstriction syndrome: case report
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3451746/
https://www.ncbi.nlm.nih.gov/pubmed/19370308
http://dx.doi.org/10.1007/s10194-009-0117-3
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