Cargando…
Human Immunodeficiency Virus-associated primary effusion lymphoma: An exceedingly rare entity in cerebrospinal fluid
Primary effusion lymphoma (PEL) in patients with Human Immunodeficiency Virus (HIV) infection may involve pleural, pericardial, and peritoneal cavities. PEL involving the cerebrospinal fluid (CSF) is exceedingly rare, and to our knowledge has only been reported in two cases. We report another case o...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630777/ https://www.ncbi.nlm.nih.gov/pubmed/26604975 http://dx.doi.org/10.4103/1742-6413.168059 |
_version_ | 1782398770062819328 |
---|---|
author | Jain, Sarika Palekar, Alka Monaco, Sara E. Craig, Fiona E. Bejjani, Ghassan Pantanowitz, Liron |
author_facet | Jain, Sarika Palekar, Alka Monaco, Sara E. Craig, Fiona E. Bejjani, Ghassan Pantanowitz, Liron |
author_sort | Jain, Sarika |
collection | PubMed |
description | Primary effusion lymphoma (PEL) in patients with Human Immunodeficiency Virus (HIV) infection may involve pleural, pericardial, and peritoneal cavities. PEL involving the cerebrospinal fluid (CSF) is exceedingly rare, and to our knowledge has only been reported in two cases. We report another case of PEL diagnosed in CSF from a 61-year-old male with Acquired Immunodeficiency Syndrome that presented with neurological symptoms. Imaging studies of his brain showed leptomeningeal/periventricular enhancement, but no mass lesion. His CSF demonstrated human herpesvirus-8 positive pleomorphic lymphoplasmacytoid cells of null cell phenotype. This case highlights that albeit rare, PEL should be included in the differential diagnosis when large atypical cells are encountered in CSF of HIV-positive patients, even when such patients have no history of lymphoma. As in this case, ancillary studies are required to make an accurate diagnosis of PEL in CSF cytology. |
format | Online Article Text |
id | pubmed-4630777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-46307772015-11-24 Human Immunodeficiency Virus-associated primary effusion lymphoma: An exceedingly rare entity in cerebrospinal fluid Jain, Sarika Palekar, Alka Monaco, Sara E. Craig, Fiona E. Bejjani, Ghassan Pantanowitz, Liron Cytojournal Case Report Primary effusion lymphoma (PEL) in patients with Human Immunodeficiency Virus (HIV) infection may involve pleural, pericardial, and peritoneal cavities. PEL involving the cerebrospinal fluid (CSF) is exceedingly rare, and to our knowledge has only been reported in two cases. We report another case of PEL diagnosed in CSF from a 61-year-old male with Acquired Immunodeficiency Syndrome that presented with neurological symptoms. Imaging studies of his brain showed leptomeningeal/periventricular enhancement, but no mass lesion. His CSF demonstrated human herpesvirus-8 positive pleomorphic lymphoplasmacytoid cells of null cell phenotype. This case highlights that albeit rare, PEL should be included in the differential diagnosis when large atypical cells are encountered in CSF of HIV-positive patients, even when such patients have no history of lymphoma. As in this case, ancillary studies are required to make an accurate diagnosis of PEL in CSF cytology. Medknow Publications & Media Pvt Ltd 2015-10-23 /pmc/articles/PMC4630777/ /pubmed/26604975 http://dx.doi.org/10.4103/1742-6413.168059 Text en Copyright: © 2015 Jain, et al.; Licensee Cytopathology Foundation Inc. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Jain, Sarika Palekar, Alka Monaco, Sara E. Craig, Fiona E. Bejjani, Ghassan Pantanowitz, Liron Human Immunodeficiency Virus-associated primary effusion lymphoma: An exceedingly rare entity in cerebrospinal fluid |
title | Human Immunodeficiency Virus-associated primary effusion lymphoma: An exceedingly rare entity in cerebrospinal fluid |
title_full | Human Immunodeficiency Virus-associated primary effusion lymphoma: An exceedingly rare entity in cerebrospinal fluid |
title_fullStr | Human Immunodeficiency Virus-associated primary effusion lymphoma: An exceedingly rare entity in cerebrospinal fluid |
title_full_unstemmed | Human Immunodeficiency Virus-associated primary effusion lymphoma: An exceedingly rare entity in cerebrospinal fluid |
title_short | Human Immunodeficiency Virus-associated primary effusion lymphoma: An exceedingly rare entity in cerebrospinal fluid |
title_sort | human immunodeficiency virus-associated primary effusion lymphoma: an exceedingly rare entity in cerebrospinal fluid |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630777/ https://www.ncbi.nlm.nih.gov/pubmed/26604975 http://dx.doi.org/10.4103/1742-6413.168059 |
work_keys_str_mv | AT jainsarika humanimmunodeficiencyvirusassociatedprimaryeffusionlymphomaanexceedinglyrareentityincerebrospinalfluid AT palekaralka humanimmunodeficiencyvirusassociatedprimaryeffusionlymphomaanexceedinglyrareentityincerebrospinalfluid AT monacosarae humanimmunodeficiencyvirusassociatedprimaryeffusionlymphomaanexceedinglyrareentityincerebrospinalfluid AT craigfionae humanimmunodeficiencyvirusassociatedprimaryeffusionlymphomaanexceedinglyrareentityincerebrospinalfluid AT bejjanighassan humanimmunodeficiencyvirusassociatedprimaryeffusionlymphomaanexceedinglyrareentityincerebrospinalfluid AT pantanowitzliron humanimmunodeficiencyvirusassociatedprimaryeffusionlymphomaanexceedinglyrareentityincerebrospinalfluid |