| Literature DB >> 30626790 |
Shinichiro Sukegawa1, Mamiko Sakata-Yanagimoto1,2, Ryota Matsuoka3, Haruka Momose1, Yusuke Kiyoki1, Masayuki Noguchi3, Naoya Nakamura4, Rei Watanabe5, Manabu Fujimoto5, Yasuhisa Yokoyama1,2, Hidekazu Nishikii1,2, Takayasu Kato1,2, Manabu Kusakabe1,2, Naoki Kurita1,2, Naoshi Obara1,2, Yuichi Hasegawa1,2, Shigeru Chiba1,2.
Abstract
Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare disease that develops with a skin lesion and is often accompanied by leukemic transformation. The normal counterparts of BPDCN tumor cells are progenitors of plasmacytoid dendritic cells, whereas the origins are thought to be hematopoietic stem cells. Approximately 10%-20% of BPDCN patients develop other hematologic malignancies, including chronic myelomonocytic leukemia (CMML). Mutations in epigenetic regulators are frequently observed in both BPDCN and CMML tumors. Azacitidine, a drug that targets epigenetic dysregulation, is known to be an effective treatment for CMML. However, it has been used in few BPDCN patients. Here, we report a BPDCN patient with skin lesions, bone marrow infiltration, and lymphadenopathy. CMML also developed during the course of BPDCN. Azacitidine had positive effects on CMML; however, BPDCN aggressively relapsed during treatment. Two TET2 mutations were found in both BPDCN and CMML tumors; one of which was commonly identified in both tumors.Entities:
Keywords: Azacitidine; BPDCN; CMML
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Year: 2018 PMID: 30626790 DOI: 10.11406/rinketsu.59.2567
Source DB: PubMed Journal: Rinsho Ketsueki ISSN: 0485-1439