首页> 外文期刊>Virchows Archiv: an international journal of pathology >Subsequent development of histiocytic sarcoma and follicular lymphoma: cytogenetics and next-generation sequencing analyses provide evidence for transdifferentiation of early common lymphoid precursor-a case report and review of literature
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Subsequent development of histiocytic sarcoma and follicular lymphoma: cytogenetics and next-generation sequencing analyses provide evidence for transdifferentiation of early common lymphoid precursor-a case report and review of literature

机译:后续发育组织细胞瘤和卵泡淋巴瘤:细胞遗传学和下一代测序分析提供了早期常见淋巴前体转型的证据 - 一种情况报告和文学审查

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摘要

Histiocytic sarcoma (HS) is a rare aggressive hematologic neoplasm that can be associated with low-grade B cell lymphoma. The development of both neoplasms is currently being considered a transdifferentiation mechanism but remains elusive. We report the case of a 65-year-old patient with synchronous development of peritoneal/abdominal HS and grade 1-2 follicular lymphoma (FL). Cytogenetic analysis and targeted next-generation sequencing of both FL and HS tumors identified common genomic alterations such as IGH-BCL2 rearrangement, CREBBP and KMT2D, and aberrations of chromosomes 9q and 19q. However, only the HS tumor had a KRAS mutation while the lymph node involved by FL harbored a TNFAIP3 mutation and both tumors also showed distinct chromosomal alterations. This report strengthens the hypothesis of a common lymphoid progenitor which accumulates genetic alterations leading to two different hematologic malignant diseases with significantly distinct prognoses.
机译:组织细胞肉瘤(HS)是一种罕见的腐蚀性血液学肿瘤,可与低级B细胞淋巴瘤相关。 目前正在考虑两个肿瘤的发展,但仍然是难以捉摸的。 我们举报了65岁的患者,腹膜/腹部HS同步发展和1-2级滤泡淋巴瘤(FL)。 FL和HS肿瘤的细胞遗传学分析和靶向下一代测序鉴定了常见的基因组改变,如IGH-BCL2重排,CREBBP和KMT2D,以及染色体9Q和19Q的像差。 然而,只有HS肿瘤的kras突变,而通过fl涉及的淋巴结留下tnfaip3突变,并且两种肿瘤也显示出明显的染色体改变。 本报告加强了常见淋巴祖的假设,该淋巴祖母含量积累了遗传改变,导致两种不同的血液学恶性疾病具有明显不同的预期。

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