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Concurrent Acute Myeloid Leukemia and T Lymphoblastic Lymphoma in a Patient with Rearranged PDGFRB Genes

Overview
Journal Diagn Pathol
Publisher Biomed Central
Specialty Pathology
Date 2012 Feb 24
PMID 22356850
Citations 8
Authors
Affiliations
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Abstract

Concurrent hematologic malignancies are relatively rare. We encountered a case of concurrent acute myeloid leukemia (AML) and T lymphoblastic lymphoma. The bone marrow chromosome analysis showed the karyotype 46, XY, t(5;12)(q33;p13), which indicated presence of PDGFRB gene translocations. Therefore, this disease belongs to the new WHO category of myeloid and lymphoid neoplasms with abnormalities in PDGFRA, PDGFRB and FGFR1 genes. Although such genetic mutations are prone to multi-lineage differentiation, the present case is in fact the first report of concurrent AML and T lymphoblastic lymphoma involving PDGFRB mutations. The patient was treated with cytarabine and daunomycin in combination with high dose dexamethasone. Allogeneic stem cell transplantation was performed after successful remission induction for both entities. The patient eventually died of chronic graft-versus-host-disease related infection. Based on such an experience, we suggest the decision of stem cell transplantation should be weighed carefully against the risks, especially when tyrosine kinase inhibitors are safe and potentially effective in dealing with such entities.

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References
1.
Capovilla M, Cayuela J, Bilhou-Nabera C, Gardin C, Letestu R, Baran-Marzak F . Synchronous FIP1L1-PDGFRA-positive chronic eosinophilic leukemia and T-cell lymphoblastic lymphoma: a bilineal clonal malignancy. Eur J Haematol. 2007; 80(1):81-6. DOI: 10.1111/j.1600-0609.2007.00973.x. View

2.
Metzgeroth G, Walz C, Score J, Siebert R, Schnittger S, Haferlach C . Recurrent finding of the FIP1L1-PDGFRA fusion gene in eosinophilia-associated acute myeloid leukemia and lymphoblastic T-cell lymphoma. Leukemia. 2007; 21(6):1183-8. DOI: 10.1038/sj.leu.2404662. View

3.
Elling C, Erben P, Walz C, Frickenhaus M, Schemionek M, Stehling M . Novel imatinib-sensitive PDGFRA-activating point mutations in hypereosinophilic syndrome induce growth factor independence and leukemia-like disease. Blood. 2011; 117(10):2935-43. DOI: 10.1182/blood-2010-05-286757. View

4.
Golub T, Barker G, Lovett M, Gilliland D . Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation. Cell. 1994; 77(2):307-16. DOI: 10.1016/0092-8674(94)90322-0. View

5.
Rathe M, Kristensen T, Moller M, Carlsen N . Myeloid neoplasm with prominent eosinophilia and PDGFRA rearrangement treated with imatinib mesylate. Pediatr Blood Cancer. 2010; 55(4):730-2. DOI: 10.1002/pbc.22655. View