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A case report of primary central nervous system lymphoma
Most patients with primary central system lymphoma (PCNSL) have immune dysfunction. PCNSL without immune dysfunction is rare and extremely challenging to diagnose. Here, we report the case of a 52-year-old woman without immune dysfunction who presented with PCNSL. The patient died a few months after...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7361490/ https://www.ncbi.nlm.nih.gov/pubmed/32660288 http://dx.doi.org/10.1177/0300060520937839 |
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author | Zeng, Xu Lu, Xiaofei Li, Xinlong Peng, Lilei Chen, Ligang |
author_facet | Zeng, Xu Lu, Xiaofei Li, Xinlong Peng, Lilei Chen, Ligang |
author_sort | Zeng, Xu |
collection | PubMed |
description | Most patients with primary central system lymphoma (PCNSL) have immune dysfunction. PCNSL without immune dysfunction is rare and extremely challenging to diagnose. Here, we report the case of a 52-year-old woman without immune dysfunction who presented with PCNSL. The patient died a few months after diagnosis and during treatment. A review of this PCNSL patient’s case highlighted that poor interpretation of imaging features and the poor correlation of laboratory test results with clinical findings led to a difficulty in making a diagnosis and administering the best treatment. For an accurate diagnosis of early stage PCNSL, positron-emission tomography computed tomography and corticosteroids should be used cautiously before stereotactic biopsy. |
format | Online Article Text |
id | pubmed-7361490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-73614902020-07-22 A case report of primary central nervous system lymphoma Zeng, Xu Lu, Xiaofei Li, Xinlong Peng, Lilei Chen, Ligang J Int Med Res Case Report Most patients with primary central system lymphoma (PCNSL) have immune dysfunction. PCNSL without immune dysfunction is rare and extremely challenging to diagnose. Here, we report the case of a 52-year-old woman without immune dysfunction who presented with PCNSL. The patient died a few months after diagnosis and during treatment. A review of this PCNSL patient’s case highlighted that poor interpretation of imaging features and the poor correlation of laboratory test results with clinical findings led to a difficulty in making a diagnosis and administering the best treatment. For an accurate diagnosis of early stage PCNSL, positron-emission tomography computed tomography and corticosteroids should be used cautiously before stereotactic biopsy. SAGE Publications 2020-07-13 /pmc/articles/PMC7361490/ /pubmed/32660288 http://dx.doi.org/10.1177/0300060520937839 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Report Zeng, Xu Lu, Xiaofei Li, Xinlong Peng, Lilei Chen, Ligang A case report of primary central nervous system lymphoma |
title | A case report of primary central nervous system lymphoma |
title_full | A case report of primary central nervous system lymphoma |
title_fullStr | A case report of primary central nervous system lymphoma |
title_full_unstemmed | A case report of primary central nervous system lymphoma |
title_short | A case report of primary central nervous system lymphoma |
title_sort | case report of primary central nervous system lymphoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7361490/ https://www.ncbi.nlm.nih.gov/pubmed/32660288 http://dx.doi.org/10.1177/0300060520937839 |
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