Yasuda Hajime, Takaku Tomoiku, Tomomatsu Junichi, Hosone Masaru, Tanaka Hiroyuki, Komatsu Norio
Division of Hematology, Department of Medicine, Juntendo University School of Medicine, Japan.
Intern Med. 2014;53(23):2717-20. doi: 10.2169/internalmedicine.53.2740. Epub 2014 Dec 1.
Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare and aggressive hematologic malignancy arising from plasmacytoid dendritic cell precursors. BPDCN typically manifests in the skin, but it can also evolve into a leukemic form or be complicated by acute myeloid leukemia, some cases with a preceding myelodysplastic syndrome (MDS). We herein report the first case of complete spontaneous regression of cutaneous BPDCN followed by acute monocytic leukemia evolving from MDS. This is also the first reported case of gastric BPDCN invasion.
母细胞性浆细胞样树突状细胞肿瘤(BPDCN)是一种罕见的侵袭性血液系统恶性肿瘤,起源于浆细胞样树突状细胞前体。BPDCN通常表现在皮肤,但也可发展为白血病形式或并发急性髓系白血病,部分病例之前有骨髓增生异常综合征(MDS)。我们在此报告首例皮肤BPDCN完全自发消退,随后发生由MDS演变而来的急性单核细胞白血病的病例。这也是首例报道的胃BPDCN浸润病例。