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T-cell/Natural killer-cell neoplasms presenting as leukemia- Case series from single tertiary care center
Background: Mature T/ NK-cell neoplasms are a rare group of disorders and their presentation as leukemia is even rarer. Most of the previous studies have focused on mature B-cell lineage leukemias and there is a paucity of data on mature T/NK-cell lineage leukemias. We, therefore, planned this study...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818784/ https://www.ncbi.nlm.nih.gov/pubmed/27047646 |
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author | Naseem, Shano Kaur, Maninderbir Sachdeva, Manupdesh Singh Ahluwalia, Jasmina Das, Reena Varma, Neelam Varma, Subhash |
author_facet | Naseem, Shano Kaur, Maninderbir Sachdeva, Manupdesh Singh Ahluwalia, Jasmina Das, Reena Varma, Neelam Varma, Subhash |
author_sort | Naseem, Shano |
collection | PubMed |
description | Background: Mature T/ NK-cell neoplasms are a rare group of disorders and their presentation as leukemia is even rarer. Most of the previous studies have focused on mature B-cell lineage leukemias and there is a paucity of data on mature T/NK-cell lineage leukemias. We, therefore, planned this study to analyze their spectrum, frequency, morphology and immunophenotypic features. Subjects and Methods: All cases of lymphomas presenting as leukemia over a period of two and a half years were evaluated. Detailed analysis of cases with T/NK-cell lineage was done for their clinical, hematological and immunophenotypic features. Results: A total of 262 cases of mature lymphoid neoplasms presented as leukemia during the study period. Of whom, only 8 (3.1%) cases were of T /NK-cell lineage and the remaining (96.9%) were of B-cell lineage. Of 8 cases, 4 (50%) had T-prolymphocytic leukemia, 2 (25%) had chronic lymphoproliferative disorder- natural killer cell and 1 (12.5%) case of each T-large granular lymphocytic leukemia and hepatosplenic γ/δ T-NHL. Conclusion: T/NK-cell leukemias are rare. Along with clinical and morphological features, pattern of immunophenotypic markers is vital for their diagnosis and subcategorization. |
format | Online Article Text |
id | pubmed-4818784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center |
record_format | MEDLINE/PubMed |
spelling | pubmed-48187842016-04-04 T-cell/Natural killer-cell neoplasms presenting as leukemia- Case series from single tertiary care center Naseem, Shano Kaur, Maninderbir Sachdeva, Manupdesh Singh Ahluwalia, Jasmina Das, Reena Varma, Neelam Varma, Subhash Int J Hematol Oncol Stem Cell Res Original Article Background: Mature T/ NK-cell neoplasms are a rare group of disorders and their presentation as leukemia is even rarer. Most of the previous studies have focused on mature B-cell lineage leukemias and there is a paucity of data on mature T/NK-cell lineage leukemias. We, therefore, planned this study to analyze their spectrum, frequency, morphology and immunophenotypic features. Subjects and Methods: All cases of lymphomas presenting as leukemia over a period of two and a half years were evaluated. Detailed analysis of cases with T/NK-cell lineage was done for their clinical, hematological and immunophenotypic features. Results: A total of 262 cases of mature lymphoid neoplasms presented as leukemia during the study period. Of whom, only 8 (3.1%) cases were of T /NK-cell lineage and the remaining (96.9%) were of B-cell lineage. Of 8 cases, 4 (50%) had T-prolymphocytic leukemia, 2 (25%) had chronic lymphoproliferative disorder- natural killer cell and 1 (12.5%) case of each T-large granular lymphocytic leukemia and hepatosplenic γ/δ T-NHL. Conclusion: T/NK-cell leukemias are rare. Along with clinical and morphological features, pattern of immunophenotypic markers is vital for their diagnosis and subcategorization. Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2016-01-01 /pmc/articles/PMC4818784/ /pubmed/27047646 Text en Copyright : © International Journal of Hematology-Oncology and Stem Cell Research & Tehran University of Medical Sciences This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Naseem, Shano Kaur, Maninderbir Sachdeva, Manupdesh Singh Ahluwalia, Jasmina Das, Reena Varma, Neelam Varma, Subhash T-cell/Natural killer-cell neoplasms presenting as leukemia- Case series from single tertiary care center |
title | T-cell/Natural killer-cell neoplasms presenting as leukemia- Case series from single tertiary care center |
title_full | T-cell/Natural killer-cell neoplasms presenting as leukemia- Case series from single tertiary care center |
title_fullStr | T-cell/Natural killer-cell neoplasms presenting as leukemia- Case series from single tertiary care center |
title_full_unstemmed | T-cell/Natural killer-cell neoplasms presenting as leukemia- Case series from single tertiary care center |
title_short | T-cell/Natural killer-cell neoplasms presenting as leukemia- Case series from single tertiary care center |
title_sort | t-cell/natural killer-cell neoplasms presenting as leukemia- case series from single tertiary care center |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818784/ https://www.ncbi.nlm.nih.gov/pubmed/27047646 |
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