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Paroxysmal nocturnal hemoglobinuria presenting as cerebral venous sinus thrombosis: a case report

Paroxysmal Nocturnal Hemoglobinuria (PNH) is a rare type of acquired hemolytic anemia that is frequently associated with thrombophilia. It may rarely present with cerebral venous sinus thrombosis, which manifests clinically with signs of raised intracranial pressure and requires lifelong anticoagula...

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Autores principales: Memon, Abdul Rauf, Khan, Rizwan, Rauf, Mohammad Uzair Abdul, Shafique, Kashif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4138960/
https://www.ncbi.nlm.nih.gov/pubmed/25143784
http://dx.doi.org/10.1186/1755-7682-7-39
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author Memon, Abdul Rauf
Khan, Rizwan
Rauf, Mohammad Uzair Abdul
Shafique, Kashif
author_facet Memon, Abdul Rauf
Khan, Rizwan
Rauf, Mohammad Uzair Abdul
Shafique, Kashif
author_sort Memon, Abdul Rauf
collection PubMed
description Paroxysmal Nocturnal Hemoglobinuria (PNH) is a rare type of acquired hemolytic anemia that is frequently associated with thrombophilia. It may rarely present with cerebral venous sinus thrombosis, which manifests clinically with signs of raised intracranial pressure and requires lifelong anticoagulation therapy. One such rare presentation was seen in a 28 years old male who had history of recurrent episodes of passing red colored urine and this time presented with severe headache. He was diagnosed to have cerebral venous sinus thrombosis and on further workup was found to be suffering from PNH.
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spelling pubmed-41389602014-08-21 Paroxysmal nocturnal hemoglobinuria presenting as cerebral venous sinus thrombosis: a case report Memon, Abdul Rauf Khan, Rizwan Rauf, Mohammad Uzair Abdul Shafique, Kashif Int Arch Med Case Report Paroxysmal Nocturnal Hemoglobinuria (PNH) is a rare type of acquired hemolytic anemia that is frequently associated with thrombophilia. It may rarely present with cerebral venous sinus thrombosis, which manifests clinically with signs of raised intracranial pressure and requires lifelong anticoagulation therapy. One such rare presentation was seen in a 28 years old male who had history of recurrent episodes of passing red colored urine and this time presented with severe headache. He was diagnosed to have cerebral venous sinus thrombosis and on further workup was found to be suffering from PNH. BioMed Central 2014-08-15 /pmc/articles/PMC4138960/ /pubmed/25143784 http://dx.doi.org/10.1186/1755-7682-7-39 Text en Copyright © 2014 Memon et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Memon, Abdul Rauf
Khan, Rizwan
Rauf, Mohammad Uzair Abdul
Shafique, Kashif
Paroxysmal nocturnal hemoglobinuria presenting as cerebral venous sinus thrombosis: a case report
title Paroxysmal nocturnal hemoglobinuria presenting as cerebral venous sinus thrombosis: a case report
title_full Paroxysmal nocturnal hemoglobinuria presenting as cerebral venous sinus thrombosis: a case report
title_fullStr Paroxysmal nocturnal hemoglobinuria presenting as cerebral venous sinus thrombosis: a case report
title_full_unstemmed Paroxysmal nocturnal hemoglobinuria presenting as cerebral venous sinus thrombosis: a case report
title_short Paroxysmal nocturnal hemoglobinuria presenting as cerebral venous sinus thrombosis: a case report
title_sort paroxysmal nocturnal hemoglobinuria presenting as cerebral venous sinus thrombosis: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4138960/
https://www.ncbi.nlm.nih.gov/pubmed/25143784
http://dx.doi.org/10.1186/1755-7682-7-39
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