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Non-Nodal CD5-Negative Mantle Cell Lymphoma with Secondary TP53 Deletion

Mantle cell lymphoma is a non-Hodgkin lymphoproliferative neoplasm with several clinical and morphologic variants linked, primarily, through genetic derangement of the cyclin D1 locus. Aberrant phenotypes have been described, though prognostic data in such cohorts are limited due to a paucity of cas...

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Detalles Bibliográficos
Autores principales: McCall, Robert K., Pang, Changlee S., Pettenati, Mark J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106885/
https://www.ncbi.nlm.nih.gov/pubmed/32257467
http://dx.doi.org/10.1155/2020/9185432
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author McCall, Robert K.
Pang, Changlee S.
Pettenati, Mark J.
author_facet McCall, Robert K.
Pang, Changlee S.
Pettenati, Mark J.
author_sort McCall, Robert K.
collection PubMed
description Mantle cell lymphoma is a non-Hodgkin lymphoproliferative neoplasm with several clinical and morphologic variants linked, primarily, through genetic derangement of the cyclin D1 locus. Aberrant phenotypes have been described, though prognostic data in such cohorts are limited due to a paucity of cases. We report a case of mantle cell lymphoma with non-nodal clinical presentation, aberrant loss of CD5 expression, and concomitant cytogenetic deletion of 17p. While non-nodal disease is often associated with an improved prognosis in mantle cell lymphoma, this 67-year-old patient experienced a more challenging clinical course with a poor initial response to chemotherapy. Therefore, this case may represent a type of non-nodal mantle cell lymphoma with a prognosis similar to that of classical cases due to the additional phenotypic and genetic alterations found in this patient.
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spelling pubmed-71068852020-04-06 Non-Nodal CD5-Negative Mantle Cell Lymphoma with Secondary TP53 Deletion McCall, Robert K. Pang, Changlee S. Pettenati, Mark J. Case Rep Hematol Case Report Mantle cell lymphoma is a non-Hodgkin lymphoproliferative neoplasm with several clinical and morphologic variants linked, primarily, through genetic derangement of the cyclin D1 locus. Aberrant phenotypes have been described, though prognostic data in such cohorts are limited due to a paucity of cases. We report a case of mantle cell lymphoma with non-nodal clinical presentation, aberrant loss of CD5 expression, and concomitant cytogenetic deletion of 17p. While non-nodal disease is often associated with an improved prognosis in mantle cell lymphoma, this 67-year-old patient experienced a more challenging clinical course with a poor initial response to chemotherapy. Therefore, this case may represent a type of non-nodal mantle cell lymphoma with a prognosis similar to that of classical cases due to the additional phenotypic and genetic alterations found in this patient. Hindawi 2020-03-18 /pmc/articles/PMC7106885/ /pubmed/32257467 http://dx.doi.org/10.1155/2020/9185432 Text en Copyright © 2020 Robert K. McCall et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
McCall, Robert K.
Pang, Changlee S.
Pettenati, Mark J.
Non-Nodal CD5-Negative Mantle Cell Lymphoma with Secondary TP53 Deletion
title Non-Nodal CD5-Negative Mantle Cell Lymphoma with Secondary TP53 Deletion
title_full Non-Nodal CD5-Negative Mantle Cell Lymphoma with Secondary TP53 Deletion
title_fullStr Non-Nodal CD5-Negative Mantle Cell Lymphoma with Secondary TP53 Deletion
title_full_unstemmed Non-Nodal CD5-Negative Mantle Cell Lymphoma with Secondary TP53 Deletion
title_short Non-Nodal CD5-Negative Mantle Cell Lymphoma with Secondary TP53 Deletion
title_sort non-nodal cd5-negative mantle cell lymphoma with secondary tp53 deletion
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106885/
https://www.ncbi.nlm.nih.gov/pubmed/32257467
http://dx.doi.org/10.1155/2020/9185432
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