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Parallel evolution of two distinct lymphoid proliferations in clonal haematopoiesis
AIMS: Angioimmunoblastic T‐cell lymphoma (AITL) is genetically characterized by TET2 and DNMT3A mutations occurring in haematopoietic progenitor cells, and late events (e.g. the RHOA‐G17V mutation) associated with malignant transformation. As TET2/DNMT3A‐mutated progenitor cells can differentiate in...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310594/ https://www.ncbi.nlm.nih.gov/pubmed/35064935 http://dx.doi.org/10.1111/his.14619 |
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author | Attygalle, Ayoma D Dobson, Rachel Chak, Pui Kwan Vroobel, Katherine M Wren, Dorte Mugalaasi, Hood Morgan, Yvonne Kaur, Manmit Ahmad, Raida Chen, Zi Naresh, Kikkeri N Du, Ming‐Qing |
author_facet | Attygalle, Ayoma D Dobson, Rachel Chak, Pui Kwan Vroobel, Katherine M Wren, Dorte Mugalaasi, Hood Morgan, Yvonne Kaur, Manmit Ahmad, Raida Chen, Zi Naresh, Kikkeri N Du, Ming‐Qing |
author_sort | Attygalle, Ayoma D |
collection | PubMed |
description | AIMS: Angioimmunoblastic T‐cell lymphoma (AITL) is genetically characterized by TET2 and DNMT3A mutations occurring in haematopoietic progenitor cells, and late events (e.g. the RHOA‐G17V mutation) associated with malignant transformation. As TET2/DNMT3A‐mutated progenitor cells can differentiate into multilineage progenies and give rise to both AITL and myeloid neoplasms, they may also have the potential to lead to other metachronous/synchronous neoplasms. We report two cases showing parallel evolution of two distinct potentially neoplastic lymphoid proliferations from a common mutated haematopoietic progenitor cell population. METHODS AND RESULTS: Both cases presented with generalized lymphadenopathy. In case 1 (a 67‐year‐old female), an initial lymph node (LN) biopsy was dismissed as reactive, but a repeat biopsy showed a nodal marginal zone lymphoma (NMZL)‐like proliferation with an increase in the number of T‐follicular helper (TFH) cells. Immunohistochemistry, and clonality and mutational analyses by targeted sequencing of both whole tissue sections and microdissected NMZL‐like lesions, demonstrated a clonal B‐cell proliferation that harboured the BRAF‐G469R mutation and shared TET2 and DNMT3A mutations with an underlying RHOA‐G17V‐mutant TFH proliferation. Review of the original LN biopsy showed histological and immunophenotypic features of AITL. In case 2 (a 66‐year‐old male), cytotoxic T‐cell lymphoma with an increase in the number of Epstein–Barr virus‐positive large B cells was diagnosed on initial biopsy. On review together with the relapsed biopsy, we identified an additional occult neoplastic TFH proliferation/smouldering AITL. Both T‐cell proliferations shared TET2 and DNMT3A mutations while RHOA‐G17V was confined to the smouldering AITL. CONCLUSIONS: In addition to demonstrating diagnostic challenges, these cases expand the potential of clonal haematopoiesis in the development of different lineage neoplastic proliferations. |
format | Online Article Text |
id | pubmed-9310594 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93105942022-07-29 Parallel evolution of two distinct lymphoid proliferations in clonal haematopoiesis Attygalle, Ayoma D Dobson, Rachel Chak, Pui Kwan Vroobel, Katherine M Wren, Dorte Mugalaasi, Hood Morgan, Yvonne Kaur, Manmit Ahmad, Raida Chen, Zi Naresh, Kikkeri N Du, Ming‐Qing Histopathology Original Articles AIMS: Angioimmunoblastic T‐cell lymphoma (AITL) is genetically characterized by TET2 and DNMT3A mutations occurring in haematopoietic progenitor cells, and late events (e.g. the RHOA‐G17V mutation) associated with malignant transformation. As TET2/DNMT3A‐mutated progenitor cells can differentiate into multilineage progenies and give rise to both AITL and myeloid neoplasms, they may also have the potential to lead to other metachronous/synchronous neoplasms. We report two cases showing parallel evolution of two distinct potentially neoplastic lymphoid proliferations from a common mutated haematopoietic progenitor cell population. METHODS AND RESULTS: Both cases presented with generalized lymphadenopathy. In case 1 (a 67‐year‐old female), an initial lymph node (LN) biopsy was dismissed as reactive, but a repeat biopsy showed a nodal marginal zone lymphoma (NMZL)‐like proliferation with an increase in the number of T‐follicular helper (TFH) cells. Immunohistochemistry, and clonality and mutational analyses by targeted sequencing of both whole tissue sections and microdissected NMZL‐like lesions, demonstrated a clonal B‐cell proliferation that harboured the BRAF‐G469R mutation and shared TET2 and DNMT3A mutations with an underlying RHOA‐G17V‐mutant TFH proliferation. Review of the original LN biopsy showed histological and immunophenotypic features of AITL. In case 2 (a 66‐year‐old male), cytotoxic T‐cell lymphoma with an increase in the number of Epstein–Barr virus‐positive large B cells was diagnosed on initial biopsy. On review together with the relapsed biopsy, we identified an additional occult neoplastic TFH proliferation/smouldering AITL. Both T‐cell proliferations shared TET2 and DNMT3A mutations while RHOA‐G17V was confined to the smouldering AITL. CONCLUSIONS: In addition to demonstrating diagnostic challenges, these cases expand the potential of clonal haematopoiesis in the development of different lineage neoplastic proliferations. John Wiley and Sons Inc. 2022-03-01 2022-04 /pmc/articles/PMC9310594/ /pubmed/35064935 http://dx.doi.org/10.1111/his.14619 Text en © 2022 The Authors. Histopathology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Attygalle, Ayoma D Dobson, Rachel Chak, Pui Kwan Vroobel, Katherine M Wren, Dorte Mugalaasi, Hood Morgan, Yvonne Kaur, Manmit Ahmad, Raida Chen, Zi Naresh, Kikkeri N Du, Ming‐Qing Parallel evolution of two distinct lymphoid proliferations in clonal haematopoiesis |
title | Parallel evolution of two distinct lymphoid proliferations in clonal haematopoiesis |
title_full | Parallel evolution of two distinct lymphoid proliferations in clonal haematopoiesis |
title_fullStr | Parallel evolution of two distinct lymphoid proliferations in clonal haematopoiesis |
title_full_unstemmed | Parallel evolution of two distinct lymphoid proliferations in clonal haematopoiesis |
title_short | Parallel evolution of two distinct lymphoid proliferations in clonal haematopoiesis |
title_sort | parallel evolution of two distinct lymphoid proliferations in clonal haematopoiesis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310594/ https://www.ncbi.nlm.nih.gov/pubmed/35064935 http://dx.doi.org/10.1111/his.14619 |
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