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Hairy Cell Leukemia: A Diagnostic Dilemma

机译:毛细胞白血病:诊断难题

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摘要

Hairy cell leukemia (HCL) is a rare chronic B-cell lymphoproliferative disorder characterized by splenomegaly without lymphadenopathy, pancytopenia, and bone marrow infiltration by an atypical cell with circumferential prominent hairy cytoplasmic projections. A high index of suspicion in such situation (splenomegaly with few atypical lymphoid cells) made us to go for bone marrow examination that revealed characteristics morphological findings of hairy cell leukemia (HCL) with increased reticulin framework. The diagnosis was confirmed when flow cytometery demonstrated positivity for hairy cell markers like CD11c,CD103 , FMC-7 and negativity for splenic lymphoma with villous lymphocytes ( SLVL) markers like CD19,CD25. Accurate diagnosis of this entity and its differentiation from other lymphoproliferative disorders is essential because of therapeutic and prognostic consideration.
机译:毛细胞白血病(HCL)是一种罕见的慢性B细胞淋巴增生性疾病,其特征是脾肿大,无淋巴结肿大,全血细胞减少和非典型细胞的骨髓浸润,周围有突出的毛状细胞质突出。在这种情况下高度怀疑(脾肿大,很少有非典型淋巴样细胞),我们去了骨髓检查,发现了网状蛋白骨架增加的毛细胞白血病(HCL)的形态学特征。当流式细胞仪对毛发细胞标记物(如CD11c,CD103,FMC-7)呈阳性,对脾脏淋巴瘤的绒毛细胞(SLVL)标记物(如CD19,CD25)呈阴性时,证实了诊断。由于治疗和预后的考虑,准确诊断该实体及其与其他淋巴增生性疾病的区别至关重要。

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