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Acute promyelocytic leukemia in early pregnancy with translocation t(15;17) and variant PML/RARA fusion transcripts

DC Field Value Language
dc.contributor.author김수정-
dc.contributor.author김진석-
dc.contributor.author박태성-
dc.contributor.author송재우-
dc.contributor.author이경아-
dc.contributor.author이승태-
dc.contributor.author최종락-
dc.date.accessioned2015-04-24T16:22:34Z-
dc.date.available2015-04-24T16:22:34Z-
dc.date.issued2009-
dc.identifier.issn0165-4608-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/103410-
dc.description.abstractA 32-year-old pregnant woman in the 13th gestational week was brought to Severance Hospital with gum bleeding and easy bruising. Initial laboratory results revealed anemia and thrombocytopenia. In a peripheral blood smear, 81% of leukocytes were large, abnormal promyelocytes. Bone marrow aspiration showed a hypercellular marrow with packed leukemic promyelocytes, and chromosome study revealed a karyotype of 46,XX,t(15;17)(q22;q21)[10]/46,XX[10]. In addition, variant fusion transcripts of PML/RARA were detected in the marrow specimen. The patient was diagnosed with acute promyelocytic leukemia (APL) and was treated with all-trans retinoic acid (ATRA) and idarubicin. One month from the patient's initial diagnosis a follow-up bone marrow examination was performed, revealing complete remission (CR). We know of no previous reports of APL during pregnancy associated with variant PML/RARA fusion transcripts. Here, we describe a novel case of APL in a pregnant woman with a t(15;17) translocation and variant fusion transcripts-
dc.description.statementOfResponsibilityopen-
dc.format.extent48~51-
dc.relation.isPartOfCANCER GENETICS AND CYTOGENETICS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHAntineoplastic Agents/therapeutic use-
dc.subject.MESHBone Marrow/pathology-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHIdarubicin/therapeutic use-
dc.subject.MESHIn Situ Hybridization, Fluorescence-
dc.subject.MESHKaryotyping-
dc.subject.MESHKorea-
dc.subject.MESHLeukemia, Promyelocytic, Acute/diagnosis-
dc.subject.MESHLeukemia, Promyelocytic, Acute/drug therapy-
dc.subject.MESHLeukemia, Promyelocytic, Acute/genetics*-
dc.subject.MESHLeukemia, Promyelocytic, Acute/pathology-
dc.subject.MESHNuclear Proteins/genetics*-
dc.subject.MESHOncogene Proteins, Fusion/genetics*-
dc.subject.MESHPregnancy-
dc.subject.MESHPregnancy Complications, Neoplastic/diagnosis-
dc.subject.MESHPregnancy Complications, Neoplastic/drug therapy-
dc.subject.MESHPregnancy Complications, Neoplastic/genetics*-
dc.subject.MESHPregnancy Complications, Neoplastic/pathology-
dc.subject.MESHPromyelocytic Leukemia Protein-
dc.subject.MESHReceptors, Retinoic Acid/genetics*-
dc.subject.MESHRetinoic Acid Receptor alpha-
dc.subject.MESHReverse Transcriptase Polymerase Chain Reaction-
dc.subject.MESHTranscription Factors/genetics*-
dc.subject.MESHTranslocation, Genetic*-
dc.subject.MESHTretinoin/therapeutic use-
dc.subject.MESHTumor Suppressor Proteins/genetics*-
dc.titleAcute promyelocytic leukemia in early pregnancy with translocation t(15;17) and variant PML/RARA fusion transcripts-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorTae Sung Park-
dc.contributor.googleauthorSeung Tae Lee-
dc.contributor.googleauthorJin Seok Kim-
dc.contributor.googleauthorJaewoo Song-
dc.contributor.googleauthorKyung-A Lee-
dc.contributor.googleauthorSue Jung Kim-
dc.contributor.googleauthorYoon-Mi Seok-
dc.contributor.googleauthorHyeon-Ji Lee-
dc.contributor.googleauthorJeong-Hyun Han-
dc.contributor.googleauthorJong-Kee Kim-
dc.contributor.googleauthorEun Yup Lee-
dc.contributor.googleauthorJong Rak Choi-
dc.identifier.doi10.1016/j.cancergencyto.2008.08.012-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00633-
dc.contributor.localIdA01017-
dc.contributor.localIdA01725-
dc.contributor.localIdA02054-
dc.contributor.localIdA02647-
dc.contributor.localIdA02930-
dc.contributor.localIdA04182-
dc.relation.journalcodeJ00443-
dc.identifier.eissn1873-4456-
dc.identifier.pmid19061780-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0165460808004901-
dc.contributor.alternativeNameKim, Soo Jeong-
dc.contributor.alternativeNameKim, Jin Seok-
dc.contributor.alternativeNamePark, Tae Sung-
dc.contributor.alternativeNameSong, Jae Woo-
dc.contributor.alternativeNameLee, Kyung A-
dc.contributor.alternativeNameLee, Seung Tae-
dc.contributor.alternativeNameChoi, Jong Rak-
dc.contributor.affiliatedAuthorKim, Soo Jeong-
dc.contributor.affiliatedAuthorKim, Jin Seok-
dc.contributor.affiliatedAuthorPark, Tae Sung-
dc.contributor.affiliatedAuthorSong, Jae Woo-
dc.contributor.affiliatedAuthorLee, Kyung A-
dc.contributor.affiliatedAuthorLee, Seung Tae-
dc.contributor.affiliatedAuthorChoi, Jong Rak-
dc.citation.volume188-
dc.citation.number1-
dc.citation.startPage48-
dc.citation.endPage51-
dc.identifier.bibliographicCitationCANCER GENETICS AND CYTOGENETICS , Vol.188(1) : 48-51, 2009-
dc.identifier.rimsid37322-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers

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