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A new therapy in Epstein-Barr virus-associated lymphoproliferative disease: a case report and a revision of the literature

BACKGROUND: Systemic chronic active Epstein-Barr virus infection is an extremely rare childhood disease. Since chronic active Epstein-Barr virus infection can trigger the onset of Epstein-Barr virus-associated lymphoproliferative disease. The clinical manifestations of the disease vary according to...

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Autores principales: Xu, Lingling, Ba, Hongjun, Lin, Hongrong, Zhong, Liangying, Li, Suping, Tang, Wen, Ke, Zhiyong, Ye, Ziyin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827238/
https://www.ncbi.nlm.nih.gov/pubmed/31685000
http://dx.doi.org/10.1186/s13052-019-0741-8
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author Xu, Lingling
Ba, Hongjun
Lin, Hongrong
Zhong, Liangying
Li, Suping
Tang, Wen
Ke, Zhiyong
Ye, Ziyin
author_facet Xu, Lingling
Ba, Hongjun
Lin, Hongrong
Zhong, Liangying
Li, Suping
Tang, Wen
Ke, Zhiyong
Ye, Ziyin
author_sort Xu, Lingling
collection PubMed
description BACKGROUND: Systemic chronic active Epstein-Barr virus infection is an extremely rare childhood disease. Since chronic active Epstein-Barr virus infection can trigger the onset of Epstein-Barr virus-associated lymphoproliferative disease. The clinical manifestations of the disease vary according to the site of involvement; therefore, management may be challenging. Currently, there are no standardized guidelines for treating Chronic active Epstein-Barr virus infection effectively. CASE PRESENTATION: We report a case of chronic active Epstein-Barr virus infection in a 5-year-old Chinese boy with intestinal, vascular, and neurological involvement. At age of 2 years and 7 months old, he had hepatomegaly and been diagnosed with Epstein-Barr virus infection. After treatment, he showed some clinical improvement. At age of 3 years and 3 months old, he presented with recurrent fever and diarrhea. Then he received methylprednisolone for 1 year and his symptoms ameliorated. At the age of 5 years, his symptoms recurred and had gastrointestinal hemorrhage and developed polyuria, frequent convulsions and hyponatremia. He was transferred to our hospital for further management. He was unconscious on admission and was diagnosised Epstein-Barr virus-lymphoproliferative disorder, based on the results in situ hybridization of EBV-encoded miRNA in sigmoid colon. Three-dimensional CT angiography demonstrated an aneurysm in the right internal carotid artery. Abdominal CT showed dilatation of vessels in part of the intestinal wall. He was also diagnosised Epstein-Barr virus encephalitis based on the elevated Epstein-Barr virus antibody titers and presence of Epstein-Barr virus DNA in the Cerebrospinal Fluid. A repeated duodenal artery embolization and symptomatic therapy could not control the hemorrhage after admission. He subsequently received treatment with ganciclovir, glucocorticoid, thalidomide, and propranolol. Hemorrhage was controlled in 5 days; his symptoms improved. The fever did not recur and the CSF pressure was also normalized. A follow-up CT at 3 months after admission showed regression of the aneurysm in the right internal carotid artery and the vascular lesion in the duodenum. DISCUSSION AND CONCLUSIONS: A new treatment protocol including thalidomide and propranolol resulted in a marked improvement in his clinical symptoms, and shows promise as a novel and effective therapeutic approach for Chronic active Epstein-Barr virus infection-associated lymphoproliferative disorder.
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spelling pubmed-68272382019-11-07 A new therapy in Epstein-Barr virus-associated lymphoproliferative disease: a case report and a revision of the literature Xu, Lingling Ba, Hongjun Lin, Hongrong Zhong, Liangying Li, Suping Tang, Wen Ke, Zhiyong Ye, Ziyin Ital J Pediatr Case Report BACKGROUND: Systemic chronic active Epstein-Barr virus infection is an extremely rare childhood disease. Since chronic active Epstein-Barr virus infection can trigger the onset of Epstein-Barr virus-associated lymphoproliferative disease. The clinical manifestations of the disease vary according to the site of involvement; therefore, management may be challenging. Currently, there are no standardized guidelines for treating Chronic active Epstein-Barr virus infection effectively. CASE PRESENTATION: We report a case of chronic active Epstein-Barr virus infection in a 5-year-old Chinese boy with intestinal, vascular, and neurological involvement. At age of 2 years and 7 months old, he had hepatomegaly and been diagnosed with Epstein-Barr virus infection. After treatment, he showed some clinical improvement. At age of 3 years and 3 months old, he presented with recurrent fever and diarrhea. Then he received methylprednisolone for 1 year and his symptoms ameliorated. At the age of 5 years, his symptoms recurred and had gastrointestinal hemorrhage and developed polyuria, frequent convulsions and hyponatremia. He was transferred to our hospital for further management. He was unconscious on admission and was diagnosised Epstein-Barr virus-lymphoproliferative disorder, based on the results in situ hybridization of EBV-encoded miRNA in sigmoid colon. Three-dimensional CT angiography demonstrated an aneurysm in the right internal carotid artery. Abdominal CT showed dilatation of vessels in part of the intestinal wall. He was also diagnosised Epstein-Barr virus encephalitis based on the elevated Epstein-Barr virus antibody titers and presence of Epstein-Barr virus DNA in the Cerebrospinal Fluid. A repeated duodenal artery embolization and symptomatic therapy could not control the hemorrhage after admission. He subsequently received treatment with ganciclovir, glucocorticoid, thalidomide, and propranolol. Hemorrhage was controlled in 5 days; his symptoms improved. The fever did not recur and the CSF pressure was also normalized. A follow-up CT at 3 months after admission showed regression of the aneurysm in the right internal carotid artery and the vascular lesion in the duodenum. DISCUSSION AND CONCLUSIONS: A new treatment protocol including thalidomide and propranolol resulted in a marked improvement in his clinical symptoms, and shows promise as a novel and effective therapeutic approach for Chronic active Epstein-Barr virus infection-associated lymphoproliferative disorder. BioMed Central 2019-11-04 /pmc/articles/PMC6827238/ /pubmed/31685000 http://dx.doi.org/10.1186/s13052-019-0741-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Xu, Lingling
Ba, Hongjun
Lin, Hongrong
Zhong, Liangying
Li, Suping
Tang, Wen
Ke, Zhiyong
Ye, Ziyin
A new therapy in Epstein-Barr virus-associated lymphoproliferative disease: a case report and a revision of the literature
title A new therapy in Epstein-Barr virus-associated lymphoproliferative disease: a case report and a revision of the literature
title_full A new therapy in Epstein-Barr virus-associated lymphoproliferative disease: a case report and a revision of the literature
title_fullStr A new therapy in Epstein-Barr virus-associated lymphoproliferative disease: a case report and a revision of the literature
title_full_unstemmed A new therapy in Epstein-Barr virus-associated lymphoproliferative disease: a case report and a revision of the literature
title_short A new therapy in Epstein-Barr virus-associated lymphoproliferative disease: a case report and a revision of the literature
title_sort new therapy in epstein-barr virus-associated lymphoproliferative disease: a case report and a revision of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827238/
https://www.ncbi.nlm.nih.gov/pubmed/31685000
http://dx.doi.org/10.1186/s13052-019-0741-8
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