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dc.contributor.author奥村, 悦久ja
dc.contributor.author大饗, 政嗣ja
dc.contributor.author白石, 裕介ja
dc.contributor.author宗田, 武ja
dc.contributor.author金丸, 洋史ja
dc.contributor.author有馬, 靖佳ja
dc.contributor.alternativeOkumura, Yoshinagaen
dc.contributor.alternativeOae, Masashien
dc.contributor.alternativeShiraishi, Yusukeen
dc.contributor.alternativeSoda, Takeshien
dc.contributor.alternativeKanamaru, Hiroshien
dc.contributor.alternativeArima, Nobuyoshien
dc.date.accessioned2016-06-20T23:49:58Z-
dc.date.available2016-06-20T23:49:58Z-
dc.date.issued2016-05-31-
dc.identifier.issn0018-1994-
dc.identifier.urihttp://hdl.handle.net/2433/215098-
dc.description.abstractA 27-year-old man visited our hospital with painless swelling of the left scrotum. Hematologic studies showed the following levels of lactate dehydrogenase, 3, 171 IU/l ; alpha-fetoprotein, 2.2 ng/ml ; and β- human chorionic gonadotropin, 0.4 ng/ml, and abdominal computed tomography revealed a mass of 10×8 ×4 cm in the left testis, and that of 3.5×3.0×5.0 cm in the left renal hilar lymph node, without any other metastasis. Left high inguinal orchiectomy was performed, and histopathological examination revealed mixed form with seminoma and teratoma. He was diagnosed to have a left germ cell tumor with left renal hilar lymph node metastases, pT1, N3, M0, stage II C, indicating poor prognosis with IGCCC. The patient received four cycles of chemotherapy, COMPE regimen (CDDP, VCR, MTX, PEP, VP-16 [etoposide]). After lactate dehydrogenase, alpha-fetoprotein, and β -human chorionic gonadotropin all normalized, retroperitoneal lymph node dissection was performed. Histopathological examination revealed only a mature teratoma. Two and half years later, hematologic studies showed blast transformation. Bone marrow biopsy revealed acute myeloblastic lymphoma (M2). The patient received one cycle of AraC and daunorubicin, one cycle of high dose AraC, and three cycles of AraC and mitoxantrone. After chemotherapy, he has maintained a disease-free status for 11 years. In this case, etoposide, a topoisomerase II inhibitor, was the presumed cause of therapy-related acute myeloid leukemia. After administering chemotherapeutic agents especially etoposide, it is important to check blood count periodically for a long time.en
dc.format.mimetypeapplication/pdf-
dc.language.isojpn-
dc.publisher泌尿器科紀要刊行会ja
dc.rights許諾条件により本文は2017/06/01に公開ja
dc.subjectGerm cell tumoren
dc.subjectTherapy related acute myeloid leukemiaen
dc.subjectEtoposideen
dc.subjectTopoisomelase II inhibitoren
dc.subject.ndc494.9-
dc.title精巣腫瘍に対するEtoposide を含む化学療法後に治療関連白血病を発症した1例ja
dc.title.alternativeTherapy-Related Acute Myeloid Leukemia Following Etoposide Based Chemotherapy in Germ Cell Tumoren
dc.typedepartmental bulletin paper-
dc.type.niitypeDepartmental Bulletin Paper-
dc.identifier.ncidAN00208315-
dc.identifier.jtitle泌尿器科紀要ja
dc.identifier.volume62-
dc.identifier.issue5-
dc.identifier.spage271-
dc.identifier.epage274-
dc.textversionpublisher-
dc.sortkey07-
dc.address北野病院泌尿器科・現: 京都大学泌尿器科ja
dc.address北野病院泌尿器科ja
dc.address北野病院泌尿器科ja
dc.address北野病院泌尿器科ja
dc.address北野病院泌尿器科ja
dc.address北野病院血液内科ja
dc.address.alternativeThe Department of Urology, Kitano Hospitalen
dc.address.alternativeThe Department of Urology, Kitano Hospitalen
dc.address.alternativeThe Department of Urology, Kitano Hospitalen
dc.address.alternativeThe Department of Urology, Kitano Hospitalen
dc.address.alternativeThe Department of Urology, Kitano Hospitalen
dc.address.alternativeThe Department of Hematology, Kitano Hospitalen
dc.identifier.pmid27320120-
dcterms.accessRightsopen access-
datacite.date.available2017-06-01-
dc.identifier.pissn0018-1994-
dc.identifier.jtitle-alternativeActa urologica Japonicala
dc.identifier.jtitle-alternativeHinyokika Kiyoen
出現コレクション:Vol.62 No.5

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