Myeloid/lymphoid neoplasms with eosinophilia and tyrosine kinase gene fusion: report of two cases with different clinical presentation.

IF 4.4 Q1 PATHOLOGY
PATHOLOGICA Pub Date : 2025-04-01 DOI:10.32074/1591-951X-975
Elisabetta Merenda, Katia Paciaroni, Emilia Scalzulli, Massimo Breccia, Stefano Licci, Luisa Bizzoni, Carla Giordano, Emma Rullo
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引用次数: 0

Abstract

Myeloid/lymphoid neoplasms with eosinophilia and tyrosine kinase gene fusions (M/LN-eo-TK) such as PDGFRA, PDGFRB, FGFR1, JAK2, FLT3 rearrangement and ETV6::ABL1 fusion include rare and heterogeneous clinical-pathological entities with some similarities, not always associated with peripheral eosinophilia. Accurate diagnosis and demonstration of the specific genetic substrate have important implications since target therapy is possibly available. Herein we report two cases showing different bone marrow features and clinical presentation. Recognition of eosinophilic granuloblasts prompted genetic analysis that showed PDGFRB (case 1) and PDGFRA (case 2) gene rearrangement. Diagnosis of M/LN-eo-TK may be challenging. Pathologists may be the first professionals to suspect the disorder and should be aware of the therapeutic implication. Accurate BOM marrow evaluation with a panel of immunohistochemical reactions, and specific molecular analyses are required for proper diagnosis.

粒细胞/淋巴肿瘤伴嗜酸性粒细胞增多和酪氨酸激酶基因融合:两例不同临床表现的报告。
粒细胞/淋巴肿瘤伴嗜酸性粒细胞增多和酪氨酸激酶基因融合(M/LN-eo-TK),如PDGFRA、PDGFRB、FGFR1、JAK2、FLT3重排和ETV6::ABL1融合,是罕见且异质性的临床病理实体,具有一些相似性,并不总是与外周嗜酸性粒细胞增多有关。准确的诊断和特定的遗传底物的证明具有重要的意义,因为靶向治疗是可能的。在此,我们报告两例具有不同骨髓特征和临床表现的病例。对嗜酸性粒细胞的识别提示基因分析显示PDGFRB(病例1)和PDGFRA(病例2)基因重排。M/LN-eo-TK的诊断可能具有挑战性。病理学家可能是最早怀疑这种疾病的专业人士,他们应该意识到这种疾病的治疗意义。准确的骨髓BOM评估与一组免疫组织化学反应,并具体的分子分析需要正确的诊断。
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来源期刊
PATHOLOGICA
PATHOLOGICA PATHOLOGY-
CiteScore
5.90
自引率
5.70%
发文量
108
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