Concurrent acute myeloid leukemia and T lymphoblastic lymphoma in a patient with rearranged PDGFRB genes
dc.contributor.author | Chang, Hung | |
dc.contributor.author | Chuang, Wen-Yu | |
dc.contributor.author | Sun, Chien-Feng | |
dc.contributor.author | Barnard, Marc R. | |
dc.date | 2022-08-11T08:09:40.000 | |
dc.date.accessioned | 2022-08-23T16:39:42Z | |
dc.date.available | 2022-08-23T16:39:42Z | |
dc.date.issued | 2012-02-22 | |
dc.date.submitted | 2012-08-27 | |
dc.identifier.citation | Diagn Pathol. 2012 Feb 22;7:19. <a href="http://dx.doi.org/10.1186/1746-1596-7-19" target="_blank">Link to article on publisher's site</a> 2012 Chang et al; licensee BioMed Central Ltd. | |
dc.identifier.issn | 1746-1596 (Linking) | |
dc.identifier.doi | 10.1186/1746-1596-7-19 | |
dc.identifier.pmid | 22356850 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14038/39531 | |
dc.description.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. | |
dc.language.iso | en_US | |
dc.relation | <a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=22356850&dopt=Abstract">Link to Article in PubMed</a> | |
dc.rights | © 2012 Chang et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. | |
dc.subject | Adult | |
dc.subject | Antineoplastic Combined Chemotherapy Protocols | |
dc.subject | Combined Modality Therapy | |
dc.subject | Cytarabine | |
dc.subject | Daunorubicin | |
dc.subject | Fatal Outcome | |
dc.subject | Graft vs Host Disease | |
dc.subject | Humans | |
dc.subject | Leukemia, Myeloid, Acute | |
dc.subject | Male | |
dc.subject | Neoplasms, Multiple Primary | |
dc.subject | Precursor Cell Lymphoblastic Leukemia-Lymphoma | |
dc.subject | Receptor, Platelet-Derived Growth Factor beta | |
dc.subject | Stem Cell Transplantation | |
dc.subject | Life Sciences | |
dc.subject | Medicine and Health Sciences | |
dc.subject | Pathology | |
dc.title | Concurrent acute myeloid leukemia and T lymphoblastic lymphoma in a patient with rearranged PDGFRB genes | |
dc.type | Journal Article | |
dc.source.journaltitle | Diagnostic pathology | |
dc.source.volume | 7 | |
dc.identifier.legacyfulltext | https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=3325&context=oapubs&unstamped=1 | |
dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/oapubs/2325 | |
dc.identifier.contextkey | 3266175 | |
refterms.dateFOA | 2022-08-23T16:39:42Z | |
html.description.abstract | <p>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.</p> | |
dc.identifier.submissionpath | oapubs/2325 | |
dc.contributor.department | Department of Medicine | |
dc.source.pages | 19 |