A Case of T-cell Acute Lymphoblastic Leukemia Relapsed As Myeloid Acute Leukemia

被引:8
作者
Paganin, Maddalena [1 ]
Buldini, Barbara [2 ]
Germano, Giuseppe [3 ]
Seganfreddo, Elena [2 ]
di Meglio, Annamaria [3 ]
Magrin, Elisa [2 ]
Grillo, Francesca [2 ]
Pigazzi, Martina [2 ,3 ]
Rizzari, Carmelo [4 ]
Cazzaniga, Giovanni [4 ]
Khiabanian, Hossein [5 ,6 ]
Palomero, Teresa [7 ,8 ]
Rabadan, Raul [5 ,6 ]
Ferrando, Adolfo A. [7 ,8 ,9 ]
Basso, Giuseppe [2 ]
机构
[1] Azienda Osped Padova, Clin Oncoematol Pediat, Padua, Italy
[2] Univ Padua, Dipartimento Salute Donna & Bambino, Padua, Italy
[3] Fdn Citta Speranza, Lab Oncoematol Pediat, Ist Ric Pediat, Fifth Floor,Corso Stati Uniti 4, I-35127 Padua, Italy
[4] Univ Milan, Ctr Ric Tettamanti, Clin Pediat, Milan, Italy
[5] Columbia Univ, Dept Syst Biol, New York, NY USA
[6] Columbia Univ, Dept Biomed Informat, New York, NY USA
[7] Columbia Univ, Inst Canc Genet, New York, NY USA
[8] Columbia Univ, Dept Pathol, New York, NY USA
[9] Columbia Univ, Dept Pediat, New York, NY 10027 USA
关键词
switch lineage; T-ALL; whole-exome sequencing; ACTIVATING MUTATIONS; LINEAGE SWITCH; CHEMOTHERAPY; TRANSPLANT; AIEOP;
D O I
10.1002/pbc.26054
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A 4-year-old male with the diagnosis of T-cell acute lymphoblastic leukemia (T-ALL) relapsed after 19 months with an acute myeloid leukemia (AML). Immunoglobulin and T-cell receptor gene rearrangements analyses reveal that both leukemias were rearranged with a clonal relationship between them. Comparative genomic hybridization (Array-CGH) and whole-exome sequencing analyses of both samples suggest that this leukemia may have originated from a common T/myeloid progenitor. The presence of homozygous deletion of p16/INK4A, p14/ARF, p15/INK4B, and heterozygous deletion of WT1 locus remained stable in the leukemia throughout phenotypic switch, revealing that this AML can be genetically associated to T-ALL.
引用
收藏
页码:1660 / 1663
页数:4
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