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Epstein–Barr Virus(+) Smooth Muscle Tumors as Manifestation of Primary Immunodeficiency Disorders
Epstein–Barr virus positive (EBV(+)) smooth muscle tumors (SMTs) constitute a very rare oncological entity. They usually develop in the context of secondary immunodeficiency caused by human immunodeficiency virus infection or immunosuppressive treatment after solid organ transplantation. However, in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835094/ https://www.ncbi.nlm.nih.gov/pubmed/29535735 http://dx.doi.org/10.3389/fimmu.2018.00368 |
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author | Magg, Thomas Schober, Tilmann Walz, Christoph Ley-Zaporozhan, Julia Facchetti, Fabio Klein, Christoph Hauck, Fabian |
author_facet | Magg, Thomas Schober, Tilmann Walz, Christoph Ley-Zaporozhan, Julia Facchetti, Fabio Klein, Christoph Hauck, Fabian |
author_sort | Magg, Thomas |
collection | PubMed |
description | Epstein–Barr virus positive (EBV(+)) smooth muscle tumors (SMTs) constitute a very rare oncological entity. They usually develop in the context of secondary immunodeficiency caused by human immunodeficiency virus infection or immunosuppressive treatment after solid organ transplantation. However, in a small fraction of predominantly pediatric patients, EBV(+) SMTs may occur in patients with primary immunodeficiency disorders (PIDs), such as GATA2 and CARMIL2 deficiency. In secondary immunodeficiencies and when the underlying condition can not be cured, the treatment of EBV(+) SMTs is based on surgery in combination with antiretroviral and reduced or altered immunosuppressive pharmacotherapy, respectively. Importantly, without definitive reconstitution of cellular immunity, long-term survival is poor. This is particularly relevant for patients with EBV(+) SMTs on the basis of PIDs. Recently, allogeneic hematopoietic stem cell transplantation resulted in cure of immunodeficiency and EBV(+) SMTs in a GATA2-deficient patient. We propose that in the absence of secondary immunodeficiency disorders patients presenting with EBV(+) SMTs should be thoroughly evaluated for PIDs. Allogeneic hematopoietic stem cell transplantation should be taken into consideration, ideally in the setting of a prospective clinical trial. |
format | Online Article Text |
id | pubmed-5835094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58350942018-03-13 Epstein–Barr Virus(+) Smooth Muscle Tumors as Manifestation of Primary Immunodeficiency Disorders Magg, Thomas Schober, Tilmann Walz, Christoph Ley-Zaporozhan, Julia Facchetti, Fabio Klein, Christoph Hauck, Fabian Front Immunol Immunology Epstein–Barr virus positive (EBV(+)) smooth muscle tumors (SMTs) constitute a very rare oncological entity. They usually develop in the context of secondary immunodeficiency caused by human immunodeficiency virus infection or immunosuppressive treatment after solid organ transplantation. However, in a small fraction of predominantly pediatric patients, EBV(+) SMTs may occur in patients with primary immunodeficiency disorders (PIDs), such as GATA2 and CARMIL2 deficiency. In secondary immunodeficiencies and when the underlying condition can not be cured, the treatment of EBV(+) SMTs is based on surgery in combination with antiretroviral and reduced or altered immunosuppressive pharmacotherapy, respectively. Importantly, without definitive reconstitution of cellular immunity, long-term survival is poor. This is particularly relevant for patients with EBV(+) SMTs on the basis of PIDs. Recently, allogeneic hematopoietic stem cell transplantation resulted in cure of immunodeficiency and EBV(+) SMTs in a GATA2-deficient patient. We propose that in the absence of secondary immunodeficiency disorders patients presenting with EBV(+) SMTs should be thoroughly evaluated for PIDs. Allogeneic hematopoietic stem cell transplantation should be taken into consideration, ideally in the setting of a prospective clinical trial. Frontiers Media S.A. 2018-02-27 /pmc/articles/PMC5835094/ /pubmed/29535735 http://dx.doi.org/10.3389/fimmu.2018.00368 Text en Copyright © 2018 Magg, Schober, Walz, Ley-Zaporozhan, Facchetti, Klein and Hauck. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Magg, Thomas Schober, Tilmann Walz, Christoph Ley-Zaporozhan, Julia Facchetti, Fabio Klein, Christoph Hauck, Fabian Epstein–Barr Virus(+) Smooth Muscle Tumors as Manifestation of Primary Immunodeficiency Disorders |
title | Epstein–Barr Virus(+) Smooth Muscle Tumors as Manifestation of Primary Immunodeficiency Disorders |
title_full | Epstein–Barr Virus(+) Smooth Muscle Tumors as Manifestation of Primary Immunodeficiency Disorders |
title_fullStr | Epstein–Barr Virus(+) Smooth Muscle Tumors as Manifestation of Primary Immunodeficiency Disorders |
title_full_unstemmed | Epstein–Barr Virus(+) Smooth Muscle Tumors as Manifestation of Primary Immunodeficiency Disorders |
title_short | Epstein–Barr Virus(+) Smooth Muscle Tumors as Manifestation of Primary Immunodeficiency Disorders |
title_sort | epstein–barr virus(+) smooth muscle tumors as manifestation of primary immunodeficiency disorders |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835094/ https://www.ncbi.nlm.nih.gov/pubmed/29535735 http://dx.doi.org/10.3389/fimmu.2018.00368 |
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