From Clinical Presentation to the Outcome: the Natural History of PML in a Portuguese Population of HIV Infected Patients

Bibliographic Details
Main Author: Nery, F.
Publication Date: 2011
Other Authors: França, M., Almeida, I., Vasconcelos, c.
Format: Article
Language: eng
Source: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Download full: http://hdl.handle.net/10400.16/864
Summary: Background Progressive multifocal leukoencephalopathy (PML) is a demyelinating disease of the central nervous system, associated with immunosuppression states. As there are only some non-published documents concerning PML in HIV infected patients in Portugal, we pretend to characterize natural history of PML infection in a population of HIV patients. Methods We retrospectively reviewed, from 1992 to 2009, PML cases in a population of 724 HIV infected patients followed in our institution. Clinical, biological, imagery features and outcomes were characterized. Results Twenty-five (3.45%) patients were identified as having PML. The mean time between HIV and PML diagnosis was 20.4 months. PML was the presentation of HIV infection in 40% of the patients, and 92% had CD4 T cell count lower than 200/mm3. Paresis was the most common clinical presentation. No specific characteristics were found in cerebrospinal fluid and JCV DNA was positive in 3 of 7 patients. MRI revealed characteristic findings. Combined antiretroviral therapy was started or changed in 96% of the patients. Neurological condition got worse in 12 patients. From the 14 deaths, 5 were directly attributed to PML progression. Follow-up was lost in 8 patients. Conclusions PML was the presentation of HIV infection in more than 1/3 of patients, frequently associated with advanced immunocompromise. MRI sensitivity to PML is high, and JCV DNA determination in CSF was not revealed to be sensible. PML diagnosis should be taken into account in HIV patients presenting any neurological symptoms, and HIV infection should be suspected when radiological findings suggest PML lesions even in previously healthy individuals.
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spelling From Clinical Presentation to the Outcome: the Natural History of PML in a Portuguese Population of HIV Infected PatientsProgressive multifocal leukoencephalopathyJC virusHumanHuman immunodeficiency virusDemyelinating diseaseBackground Progressive multifocal leukoencephalopathy (PML) is a demyelinating disease of the central nervous system, associated with immunosuppression states. As there are only some non-published documents concerning PML in HIV infected patients in Portugal, we pretend to characterize natural history of PML infection in a population of HIV patients. Methods We retrospectively reviewed, from 1992 to 2009, PML cases in a population of 724 HIV infected patients followed in our institution. Clinical, biological, imagery features and outcomes were characterized. Results Twenty-five (3.45%) patients were identified as having PML. The mean time between HIV and PML diagnosis was 20.4 months. PML was the presentation of HIV infection in 40% of the patients, and 92% had CD4 T cell count lower than 200/mm3. Paresis was the most common clinical presentation. No specific characteristics were found in cerebrospinal fluid and JCV DNA was positive in 3 of 7 patients. MRI revealed characteristic findings. Combined antiretroviral therapy was started or changed in 96% of the patients. Neurological condition got worse in 12 patients. From the 14 deaths, 5 were directly attributed to PML progression. Follow-up was lost in 8 patients. Conclusions PML was the presentation of HIV infection in more than 1/3 of patients, frequently associated with advanced immunocompromise. MRI sensitivity to PML is high, and JCV DNA determination in CSF was not revealed to be sensible. PML diagnosis should be taken into account in HIV patients presenting any neurological symptoms, and HIV infection should be suspected when radiological findings suggest PML lesions even in previously healthy individuals.Elmer PressRepositório Científico do Centro Hospitalar Universitário de Santo AntónioNery, F.França, M.Almeida, I.Vasconcelos, c.2011-11-10T07:53:32Z2011-02-122011-02-12T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.16/864engJ Clin Med Res. 2011 February 12; 3(1): 17–22.1918-3003info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-10-20T10:54:09Zoai:repositorio.chporto.pt:10400.16/864Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:37:25.514582Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv From Clinical Presentation to the Outcome: the Natural History of PML in a Portuguese Population of HIV Infected Patients
title From Clinical Presentation to the Outcome: the Natural History of PML in a Portuguese Population of HIV Infected Patients
spellingShingle From Clinical Presentation to the Outcome: the Natural History of PML in a Portuguese Population of HIV Infected Patients
Nery, F.
Progressive multifocal leukoencephalopathy
JC virus
HumanHuman immunodeficiency virus
Demyelinating disease
title_short From Clinical Presentation to the Outcome: the Natural History of PML in a Portuguese Population of HIV Infected Patients
title_full From Clinical Presentation to the Outcome: the Natural History of PML in a Portuguese Population of HIV Infected Patients
title_fullStr From Clinical Presentation to the Outcome: the Natural History of PML in a Portuguese Population of HIV Infected Patients
title_full_unstemmed From Clinical Presentation to the Outcome: the Natural History of PML in a Portuguese Population of HIV Infected Patients
title_sort From Clinical Presentation to the Outcome: the Natural History of PML in a Portuguese Population of HIV Infected Patients
author Nery, F.
author_facet Nery, F.
França, M.
Almeida, I.
Vasconcelos, c.
author_role author
author2 França, M.
Almeida, I.
Vasconcelos, c.
author2_role author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Centro Hospitalar Universitário de Santo António
dc.contributor.author.fl_str_mv Nery, F.
França, M.
Almeida, I.
Vasconcelos, c.
dc.subject.por.fl_str_mv Progressive multifocal leukoencephalopathy
JC virus
HumanHuman immunodeficiency virus
Demyelinating disease
topic Progressive multifocal leukoencephalopathy
JC virus
HumanHuman immunodeficiency virus
Demyelinating disease
description Background Progressive multifocal leukoencephalopathy (PML) is a demyelinating disease of the central nervous system, associated with immunosuppression states. As there are only some non-published documents concerning PML in HIV infected patients in Portugal, we pretend to characterize natural history of PML infection in a population of HIV patients. Methods We retrospectively reviewed, from 1992 to 2009, PML cases in a population of 724 HIV infected patients followed in our institution. Clinical, biological, imagery features and outcomes were characterized. Results Twenty-five (3.45%) patients were identified as having PML. The mean time between HIV and PML diagnosis was 20.4 months. PML was the presentation of HIV infection in 40% of the patients, and 92% had CD4 T cell count lower than 200/mm3. Paresis was the most common clinical presentation. No specific characteristics were found in cerebrospinal fluid and JCV DNA was positive in 3 of 7 patients. MRI revealed characteristic findings. Combined antiretroviral therapy was started or changed in 96% of the patients. Neurological condition got worse in 12 patients. From the 14 deaths, 5 were directly attributed to PML progression. Follow-up was lost in 8 patients. Conclusions PML was the presentation of HIV infection in more than 1/3 of patients, frequently associated with advanced immunocompromise. MRI sensitivity to PML is high, and JCV DNA determination in CSF was not revealed to be sensible. PML diagnosis should be taken into account in HIV patients presenting any neurological symptoms, and HIV infection should be suspected when radiological findings suggest PML lesions even in previously healthy individuals.
publishDate 2011
dc.date.none.fl_str_mv 2011-11-10T07:53:32Z
2011-02-12
2011-02-12T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.16/864
url http://hdl.handle.net/10400.16/864
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv J Clin Med Res. 2011 February 12; 3(1): 17–22.
1918-3003
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv Elmer Press
publisher.none.fl_str_mv Elmer Press
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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