Transformation of T-Cell Acute Lymphoblastic Lymphoma to Peripheral T-Cell Lymphoma: A Report of Two Cases
Nonhepatosplenic/noncutaneous γδ peripheral T-cell lymphoma (NHNCγδ PTCL) represents a miscellaneous group of unrelated T-cell lymphomas of which only isolated cases have been reported. We describe two cases of transformation from T-lymphoblastic leukemia/lymphoma to NHNCγδ PTCL. Transformation into...
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doaj-30abd389bd9a4299b5e1fff60934e8d52020-11-24T21:01:11ZengHindawi LimitedCase Reports in Hematology2090-65602090-65792018-01-01201810.1155/2018/91915829191582Transformation of T-Cell Acute Lymphoblastic Lymphoma to Peripheral T-Cell Lymphoma: A Report of Two CasesMichael Markow0Abu-Sayeef Mirza1Lia Perez2Haipeng Shao3Pedro Horna4Claudio Anasetti5Lubomir Sokol6Mohammad O. Hussaini7Department of Pathology, Ohio State University, Columbus, OH, USADepartment of Internal Medicine, University of South Florida, Tampa, FL, USABone Marrow Transplant Program, Moffitt Cancer Center, Tampa, FL, USAMoffitt Cancer Center, Tampa, FL, USAMayo Clinic, Rochester, MN, USAMoffitt Cancer Center, Tampa, FL, USAMoffitt Cancer Center, Tampa, FL, USAMoffitt Cancer Center, Tampa, FL, USANonhepatosplenic/noncutaneous γδ peripheral T-cell lymphoma (NHNCγδ PTCL) represents a miscellaneous group of unrelated T-cell lymphomas of which only isolated cases have been reported. We describe two cases of transformation from T-lymphoblastic leukemia/lymphoma to NHNCγδ PTCL. Transformation into more aggressive disease is a rare event in T-cell lineage-derived hematologic malignancies compared to B-cell neoplasms. Nevertheless, both of our cases involved relapse as PTCL manifested with skin involvement and an overt shift from blastic morphology to large granular leukemia-like mature T cells. Among other notable molecular characteristics, expression of immature markers such as TdT was lost in both cases. Based on cytogenetics, phenotype, and morphology, both patients represent a novel phenomenon of clonal transformation from T-ALL to PTCL which has rarely been reported in the literature. Such transformation may carry important diagnostic and biological implications.http://dx.doi.org/10.1155/2018/9191582 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Michael Markow Abu-Sayeef Mirza Lia Perez Haipeng Shao Pedro Horna Claudio Anasetti Lubomir Sokol Mohammad O. Hussaini |
spellingShingle |
Michael Markow Abu-Sayeef Mirza Lia Perez Haipeng Shao Pedro Horna Claudio Anasetti Lubomir Sokol Mohammad O. Hussaini Transformation of T-Cell Acute Lymphoblastic Lymphoma to Peripheral T-Cell Lymphoma: A Report of Two Cases Case Reports in Hematology |
author_facet |
Michael Markow Abu-Sayeef Mirza Lia Perez Haipeng Shao Pedro Horna Claudio Anasetti Lubomir Sokol Mohammad O. Hussaini |
author_sort |
Michael Markow |
title |
Transformation of T-Cell Acute Lymphoblastic Lymphoma to Peripheral T-Cell Lymphoma: A Report of Two Cases |
title_short |
Transformation of T-Cell Acute Lymphoblastic Lymphoma to Peripheral T-Cell Lymphoma: A Report of Two Cases |
title_full |
Transformation of T-Cell Acute Lymphoblastic Lymphoma to Peripheral T-Cell Lymphoma: A Report of Two Cases |
title_fullStr |
Transformation of T-Cell Acute Lymphoblastic Lymphoma to Peripheral T-Cell Lymphoma: A Report of Two Cases |
title_full_unstemmed |
Transformation of T-Cell Acute Lymphoblastic Lymphoma to Peripheral T-Cell Lymphoma: A Report of Two Cases |
title_sort |
transformation of t-cell acute lymphoblastic lymphoma to peripheral t-cell lymphoma: a report of two cases |
publisher |
Hindawi Limited |
series |
Case Reports in Hematology |
issn |
2090-6560 2090-6579 |
publishDate |
2018-01-01 |
description |
Nonhepatosplenic/noncutaneous γδ peripheral T-cell lymphoma (NHNCγδ PTCL) represents a miscellaneous group of unrelated T-cell lymphomas of which only isolated cases have been reported. We describe two cases of transformation from T-lymphoblastic leukemia/lymphoma to NHNCγδ PTCL. Transformation into more aggressive disease is a rare event in T-cell lineage-derived hematologic malignancies compared to B-cell neoplasms. Nevertheless, both of our cases involved relapse as PTCL manifested with skin involvement and an overt shift from blastic morphology to large granular leukemia-like mature T cells. Among other notable molecular characteristics, expression of immature markers such as TdT was lost in both cases. Based on cytogenetics, phenotype, and morphology, both patients represent a novel phenomenon of clonal transformation from T-ALL to PTCL which has rarely been reported in the literature. Such transformation may carry important diagnostic and biological implications. |
url |
http://dx.doi.org/10.1155/2018/9191582 |
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