Myeloid and lymphoid neoplasm with novel complex translocation: unusual case report with T-lymphoblastic lymphoma, myeloid hyperplasia, eosinophilia, basophilia, and t(1;8;10)( (p31;q24;q11.2).

Mansour S Aljabry
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Abstract

Myeloid and lymphoid neoplasms with eosinophilia (M/Ls-Eo) encompass heterogeneous but aggressive hematopoietic disorders triggered by fusion genes or mutations that typically lead to constitutive overexpression of tyrosine kinase. The occurrence of T-lymphoblastic lymphoma in the setting of M/Ls-Eo has been reported rarely in the literature. Herein, we present an unusual case of a 28-year-old male patient who presented with massive lymphadenopathy and T-lymphoblastic lymphoma in the lymph node occurring concurrently with myeloid hyperplasia, eosinophilia and basophilia in peripheral blood and bone marrow biopsy. The syndrome was associated with a novel complex karyotype involving der(8)t(1;8;10)(p31;q24;q11.2). The FISH study was negative for BCR::ABL1, JAK2, PDGFRA, PDGFRB, and FGFR1 rearrangements. The patient's clinical course was aggressive and resistant to multiple lines of intensive chemotherapy regimens. Therefore, he underwent allogenic stem cell transplantation with a fully matched donor. A brief review of the occurrence of T-LBL in conjunction with M/Ls-Eo neoplasm was made with a special focus on molecular aspects.

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伴有新型复合易位的骨髓和淋巴肿瘤:伴有T淋巴细胞淋巴瘤、骨髓增生症、嗜酸性粒细胞增多症、嗜碱性粒细胞增多症和t(1;8;10)((p31;q24;q11.2)的罕见病例报告。
嗜酸性粒细胞和淋巴细胞肿瘤(M/Ls-Eo)包括由融合基因或突变引发的异质性侵袭性造血疾病,这些基因或突变通常会导致酪氨酸激酶的组成性过表达。文献中很少报道在M/Ls-Eo的情况下发生T淋巴细胞淋巴瘤。在此,我们介绍了一例不寻常的病例:一名 28 岁的男性患者出现大量淋巴结肿大,淋巴结中出现 T 淋巴细胞淋巴瘤,同时外周血和骨髓活检中出现骨髓增生、嗜酸性粒细胞增多和嗜碱性粒细胞增多。该综合征与新的复杂核型有关,涉及der(8)t(1;8;10)(p31;q24;q11.2)。FISH检查结果显示,BCR::ABL1、JAK2、PDGFRA、PDGFRB和FGFR1重排均为阴性。患者的临床病程具有侵袭性,对多线强化化疗方案产生耐药性。因此,他接受了完全匹配供体的异基因干细胞移植。本文简要回顾了T-LBL与M/Ls-Eo肿瘤的结合情况,并特别关注了分子方面的问题。
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