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Epstein-Barr virus myelitis and Castleman's disease in a patient with acquired immune deficiency syndrome: a case report
INTRODUCTION: Few cases of Epstein-Barr virus myelitis have been described in the literature. Multi-centric Castleman's disease is a lymphoproliferative disorder that is well known for its associations with the human immunodeficiency virus, human herpes virus 8, and Kaposi's sarcoma. The c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3128854/ https://www.ncbi.nlm.nih.gov/pubmed/21615962 http://dx.doi.org/10.1186/1752-1947-5-209 |
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author | Albany, Costantine Psevdos, George Balderacchi, Jasminka Sharp, Victoria L |
author_facet | Albany, Costantine Psevdos, George Balderacchi, Jasminka Sharp, Victoria L |
author_sort | Albany, Costantine |
collection | PubMed |
description | INTRODUCTION: Few cases of Epstein-Barr virus myelitis have been described in the literature. Multi-centric Castleman's disease is a lymphoproliferative disorder that is well known for its associations with the human immunodeficiency virus, human herpes virus 8, and Kaposi's sarcoma. The concurrent presentation of these two diseases in a patient at the same time is extremely unusual. CASE PRESENTATION: We describe the case of a 43-year-old Caucasian man with acquired immune deficiency syndrome who presented with fever, weight loss and diffuse lymphadenopathy, and was diagnosed with multi-centric Castleman's disease. He presented three weeks later with lower extremity weakness and urinary retention, at which time cerebrospinal fluid contained lymphocytic pleocytosis and elevated protein. Magnetic resonance imaging demonstrated abnormal spinal cord signal intensity over several cervical and thoracic segments, suggesting the diagnosis of myelitis. Our patient was ultimately diagnosed with Epstein-Barr virus myelitis, as Epstein-Barr virus DNA was detected by polymerase chain reaction in the cerebrospinal fluid. CONCLUSION: To the best of our knowledge, this is the first case of multi-centric Castleman's disease followed by acute Epstein-Barr virus myelitis in a human immunodeficiency virus-infected patient. Clinicians caring for human immunodeficiency virus-infected patients should be vigilant about monitoring patients with increasing lymphadenopathy, prompting thorough diagnostic investigations when necessary. |
format | Online Article Text |
id | pubmed-3128854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31288542011-07-04 Epstein-Barr virus myelitis and Castleman's disease in a patient with acquired immune deficiency syndrome: a case report Albany, Costantine Psevdos, George Balderacchi, Jasminka Sharp, Victoria L J Med Case Reports Case Report INTRODUCTION: Few cases of Epstein-Barr virus myelitis have been described in the literature. Multi-centric Castleman's disease is a lymphoproliferative disorder that is well known for its associations with the human immunodeficiency virus, human herpes virus 8, and Kaposi's sarcoma. The concurrent presentation of these two diseases in a patient at the same time is extremely unusual. CASE PRESENTATION: We describe the case of a 43-year-old Caucasian man with acquired immune deficiency syndrome who presented with fever, weight loss and diffuse lymphadenopathy, and was diagnosed with multi-centric Castleman's disease. He presented three weeks later with lower extremity weakness and urinary retention, at which time cerebrospinal fluid contained lymphocytic pleocytosis and elevated protein. Magnetic resonance imaging demonstrated abnormal spinal cord signal intensity over several cervical and thoracic segments, suggesting the diagnosis of myelitis. Our patient was ultimately diagnosed with Epstein-Barr virus myelitis, as Epstein-Barr virus DNA was detected by polymerase chain reaction in the cerebrospinal fluid. CONCLUSION: To the best of our knowledge, this is the first case of multi-centric Castleman's disease followed by acute Epstein-Barr virus myelitis in a human immunodeficiency virus-infected patient. Clinicians caring for human immunodeficiency virus-infected patients should be vigilant about monitoring patients with increasing lymphadenopathy, prompting thorough diagnostic investigations when necessary. BioMed Central 2011-05-27 /pmc/articles/PMC3128854/ /pubmed/21615962 http://dx.doi.org/10.1186/1752-1947-5-209 Text en Copyright ©2011 Albany et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Albany, Costantine Psevdos, George Balderacchi, Jasminka Sharp, Victoria L Epstein-Barr virus myelitis and Castleman's disease in a patient with acquired immune deficiency syndrome: a case report |
title | Epstein-Barr virus myelitis and Castleman's disease in a patient with acquired immune deficiency syndrome: a case report |
title_full | Epstein-Barr virus myelitis and Castleman's disease in a patient with acquired immune deficiency syndrome: a case report |
title_fullStr | Epstein-Barr virus myelitis and Castleman's disease in a patient with acquired immune deficiency syndrome: a case report |
title_full_unstemmed | Epstein-Barr virus myelitis and Castleman's disease in a patient with acquired immune deficiency syndrome: a case report |
title_short | Epstein-Barr virus myelitis and Castleman's disease in a patient with acquired immune deficiency syndrome: a case report |
title_sort | epstein-barr virus myelitis and castleman's disease in a patient with acquired immune deficiency syndrome: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3128854/ https://www.ncbi.nlm.nih.gov/pubmed/21615962 http://dx.doi.org/10.1186/1752-1947-5-209 |
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