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一名急性巨核细胞白血病患儿中的一种新型变异型t(1;22)易位——插入(22;1)(q13;p13p31)

A Novel Variant t(1;22) Translocation - ins(22;1)(q13;p13p31) - in a Child with Acute Megakaryoblastic Leukemia.

作者信息

Margolskee Elizabeth, Saab Jad, Geyer Julia T, Aledo Alexander, Mathew Susan

机构信息

Department of Pathology and Laboratory Medicine, Weill Cornell Medicine/New York Presbyterian Hospital, New York, NY, USA.

Department of Pediatrics, Weill Cornell Medicine/New York Presbyterian Hospital, New York, NY, USA.

出版信息

Am J Case Rep. 2017 Apr 19;18:422-426. doi: 10.12659/ajcr.901855.

Abstract

BACKGROUND The reciprocal translocation t(1;22)(p13;q13) involving the RBM15 and MKL1 genes is an uncommon abnormality that occurs in a subset of acute myeloid leukemia with megakaryocytic differentiation (AMKL). Variant translocations have been infrequently described in this subtype of leukemia. CASE REPORT We describe the case of a 3-month-old girl who presented with progressive abdominal distension, vomiting, and fever. Although there was no morphologic evidence of leukemia in the bone marrow, cytogenetic and metaphase fluorescence in situ hybridization analysis identified an insertion of p13p31 bands of chromosome 1 onto the long arm of chromosome 22, resulting in the karyotype: 46,XX,ins(22;1)(q13;p13p31). Subsequent liver biopsy demonstrated extensive involvement by AMKL. CONCLUSIONS AMKL can present with fewer than 20% blasts in the peripheral blood or bone marrow, necessitating careful evaluation for extramedullary disease. In other situations, bone marrow fibrosis can result in difficult marrow aspirations and a falsely decreased blast count. This case report highlights the critical role of careful cytogenetic and FISH testing in the diagnosis of AMKL.

摘要

背景

涉及RBM15和MKL1基因的相互易位t(1;22)(p13;q13)是一种罕见的异常情况,发生于一部分具有巨核细胞分化的急性髓系白血病(AMKL)中。在这种白血病亚型中,变异易位很少被描述。病例报告:我们描述了一名3个月大女孩的病例,她出现进行性腹胀、呕吐和发热。尽管骨髓中没有白血病的形态学证据,但细胞遗传学和中期荧光原位杂交分析确定1号染色体的p13p31带插入到22号染色体长臂上,导致核型为:46,XX,ins(22;1)(q13;p13p31)。随后的肝脏活检显示AMKL广泛浸润。结论:AMKL在外周血或骨髓中的原始细胞可能少于20%,因此需要仔细评估髓外疾病。在其他情况下,骨髓纤维化可能导致骨髓穿刺困难和原始细胞计数假性降低。本病例报告强调了仔细的细胞遗传学和荧光原位杂交检测在AMKL诊断中的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f3d/5404477/0fe92d2541c5/amjcaserep-18-422-g001.jpg

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