TY - JOUR
T1 - The development of T-cell malignancies in patients with pre-existing myeloproliferative neoplasms
T2 - A report of three cases
AU - Burns, Ethan A.
AU - Anand, Kartik
AU - Chung, Betty
AU - Shah, Shilpan
AU - Randhawa, Jasleen K.
AU - Pingali, Sai Ravi
N1 - Publisher Copyright:
© 2020 ecancer Global Foundation. All rights reserved.
PY - 2020
Y1 - 2020
N2 - Secondary acute myeloid leukaemia complicating the natural disease course of preexisting Philadelphia chromosome-negative myeloproliferative neoplasms (PN-MPN) is well documented and associated with treatment challenges and significant morbidity. The incidence of a T-cell malignancy developing in patients with pre-existing PN-MPN is uncommon, with one case documented in the literature. We present two cases of angioimmunoblastic T-cell lymphoma (AITL) and one case of T-cell acute lymphoblastic leukaemia (T-ALL) that developed in patients with essential thrombocythemia (ET) and primary myelofibrosis (PMF), respectively. All malignancies were advanced at diagnosis and exhibited disease progression, regardless of the mutational status of the underlying ET/PMF, presence of cytogenetic abnormalities, type of T-cell neoplasm or systemic chemotherapy utilised. The median time to diagnosis of AITL or T-ALL from the onset of MPN was 4.5 years (range: 6 months-10 years). This single institutional case series demonstrates the possibility of an association between T-cell neoplasms and PN-MPNs.
AB - Secondary acute myeloid leukaemia complicating the natural disease course of preexisting Philadelphia chromosome-negative myeloproliferative neoplasms (PN-MPN) is well documented and associated with treatment challenges and significant morbidity. The incidence of a T-cell malignancy developing in patients with pre-existing PN-MPN is uncommon, with one case documented in the literature. We present two cases of angioimmunoblastic T-cell lymphoma (AITL) and one case of T-cell acute lymphoblastic leukaemia (T-ALL) that developed in patients with essential thrombocythemia (ET) and primary myelofibrosis (PMF), respectively. All malignancies were advanced at diagnosis and exhibited disease progression, regardless of the mutational status of the underlying ET/PMF, presence of cytogenetic abnormalities, type of T-cell neoplasm or systemic chemotherapy utilised. The median time to diagnosis of AITL or T-ALL from the onset of MPN was 4.5 years (range: 6 months-10 years). This single institutional case series demonstrates the possibility of an association between T-cell neoplasms and PN-MPNs.
KW - Angioimmunoblastic T-cell lymphoma
KW - Essential thrombocythemia
KW - Philadelphia negative myeloproliferative neoplasm
KW - Polycythemia vera
KW - Primary myelofibrosis
KW - T-cell acute lymphoblastic leukaemia
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U2 - 10.3332/ECANCER.2020.1011
DO - 10.3332/ECANCER.2020.1011
M3 - Article
AN - SCOPUS:85107508808
SN - 1754-6605
VL - 14
JO - ecancermedicalscience
JF - ecancermedicalscience
M1 - 1011
ER -