t(6;8)(q27;p12)和FGFR1OP-FGFR1融合患者的临床变异性:另外两例。

José L Vizmanos, Roberto Hernández, María J Vidal, María J Larráyoz, María D Odero, Julián Marín, María T Ardanaz, María J Calasanz, Nicholas C P Cross
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引用次数: 54

摘要

我们报告了两例t(6;8)(q27;p12)和FGFR1OP-FGFR1融合的新病例。病例1表现为真性红细胞增多症(PV),并在4年内发展为类似8p11骨髓增生性综合征(EMS)的骨髓增生性疾病(MPD)。病例2表现为b淋巴细胞白血病(B-ALL)。这些病例说明在FGFR1重排患者中观察到的临床异质性,并表明组成型激活酪氨酸激酶可能在mpd中更为普遍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical variability of patients with the t(6;8)(q27;p12) and FGFR1OP-FGFR1 fusion: two further cases.

We report two new cases with the t(6;8)(q27;p12) and FGFR1OP-FGFR1 fusion. Case 1 presented with polycythaemia vera (PV) and evolved over 4 years to a myeloproliferative disorder (MPD) resembling the 8p11 myeloproliferative syndrome (EMS). Case 2 presented with B-cell lymphoblastic leukaemia (B-ALL). These cases illustrate the clinical heterogeneity observed in patients with FGFR1 rearrangements and suggest that constitutively activated tyrosine kinases may be more widespread in MPDs.

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