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Work-up and management of a high-risk patient with primary central nervous system lymphoma
Primary central nervous system lymphoma (PCNSL) is a rare disorder that, in 95% of cases, represents diffuse large B-cell lymphoma. As such, making an accurate diagnosis is important. At present, stereotactic-guided biopsy is a recognized method of choice for tissue analysis. However, the diagnostic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Chinese Anti-Cancer Association
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5250610/ https://www.ncbi.nlm.nih.gov/pubmed/28154784 http://dx.doi.org/10.20892/j.issn.2095-3941.2016.0070 |
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author | Zeynalova, Pervin A. Tumyan, Gayane S. Dolgushin, Mikhail B. Akhmedov, Mobil I. |
author_facet | Zeynalova, Pervin A. Tumyan, Gayane S. Dolgushin, Mikhail B. Akhmedov, Mobil I. |
author_sort | Zeynalova, Pervin A. |
collection | PubMed |
description | Primary central nervous system lymphoma (PCNSL) is a rare disorder that, in 95% of cases, represents diffuse large B-cell lymphoma. As such, making an accurate diagnosis is important. At present, stereotactic-guided biopsy is a recognized method of choice for tissue analysis. However, the diagnostic work-up for high-risk patients is determined by their performance status. Here, we report a case of PCNSL in a high-risk patient, for whom diagnosis was established by cerebrospinal fluid cytology and flow cytometry, which significantly shortened a diagnostic work-up period and allowed for the immediate treatment of the patient. |
format | Online Article Text |
id | pubmed-5250610 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Chinese Anti-Cancer Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-52506102017-02-02 Work-up and management of a high-risk patient with primary central nervous system lymphoma Zeynalova, Pervin A. Tumyan, Gayane S. Dolgushin, Mikhail B. Akhmedov, Mobil I. Cancer Biol Med Case Report Primary central nervous system lymphoma (PCNSL) is a rare disorder that, in 95% of cases, represents diffuse large B-cell lymphoma. As such, making an accurate diagnosis is important. At present, stereotactic-guided biopsy is a recognized method of choice for tissue analysis. However, the diagnostic work-up for high-risk patients is determined by their performance status. Here, we report a case of PCNSL in a high-risk patient, for whom diagnosis was established by cerebrospinal fluid cytology and flow cytometry, which significantly shortened a diagnostic work-up period and allowed for the immediate treatment of the patient. Chinese Anti-Cancer Association 2016-12 /pmc/articles/PMC5250610/ /pubmed/28154784 http://dx.doi.org/10.20892/j.issn.2095-3941.2016.0070 Text en Copyright 2016 Cancer Biology & Medicine http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Case Report Zeynalova, Pervin A. Tumyan, Gayane S. Dolgushin, Mikhail B. Akhmedov, Mobil I. Work-up and management of a high-risk patient with primary central nervous system lymphoma |
title | Work-up and management of a high-risk patient with primary central nervous system lymphoma |
title_full | Work-up and management of a high-risk patient with primary central nervous system lymphoma |
title_fullStr | Work-up and management of a high-risk patient with primary central nervous system lymphoma |
title_full_unstemmed | Work-up and management of a high-risk patient with primary central nervous system lymphoma |
title_short | Work-up and management of a high-risk patient with primary central nervous system lymphoma |
title_sort | work-up and management of a high-risk patient with primary central nervous system lymphoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5250610/ https://www.ncbi.nlm.nih.gov/pubmed/28154784 http://dx.doi.org/10.20892/j.issn.2095-3941.2016.0070 |
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