Matsumoto K, Morita K, Takada S, Sakura T, Shiozaki H, Murakami H, Miyawaki S
Department of Internal Medicine, Saiseikai Maebashi Hospital, Maebashi, Japan.
Int J Hematol. 1999 Dec;70(4):278-82.
A 40-year-old male patient presented with leukocytosis and mild splenomegaly. Bone marrow aspirate showed myeloid hyperplasia and eosinophilia resembling chronic myelogenous leukemia in the chronic phase. Cytogenetic examination of bone marrow cells revealed an unusual karyotype, t(8;13)(p11;q12), in 20/20 metaphases. Not the BCR/ABL, but the ZNF198/FGFR1 chimeric mRNA was detected by reverse transcription-polymerase chain reaction. Since 1992, 12 patients with a similar atypical myeloproliferative disorder with T-cell non-Hodgkin's lymphoma or eosinophilia, associated with a t(8;13) translocation in both bone marrow and lymph node specimens, have been described. The present case is an additional one that should be classified into this new clinicopathologic entity.
一名40岁男性患者出现白细胞增多和轻度脾肿大。骨髓穿刺显示骨髓增生和嗜酸性粒细胞增多,类似于慢性期慢性粒细胞白血病。骨髓细胞的细胞遗传学检查显示,在20个中期相中,有一个异常核型t(8;13)(p11;q12)。通过逆转录-聚合酶链反应检测到的不是BCR/ABL,而是ZNF198/FGFR1嵌合mRNA。自1992年以来,已有12例患者被描述为患有类似的非典型骨髓增殖性疾病,伴有T细胞非霍奇金淋巴瘤或嗜酸性粒细胞增多,骨髓和淋巴结标本中均有t(8;13)易位。本病例是应归类为这一新的临床病理实体的又一病例。