Primary Low-Grade Fibromyxoid Sarcoma of the Kidney in a Child with the Alternative EWSR1-CREB3L1 Gene Fusion

被引:19
|
作者
Rubinstein, Jill C. [1 ]
Visa, Arjun [2 ]
Zhang, Lei [3 ]
Antonescu, Cristina R. [3 ]
Christison-Lagay, Emily R. [4 ]
Morotti, Raffaella [5 ]
机构
[1] Yale Univ, Sch Med, Dept Gen Surg, New Haven, CT USA
[2] Univ Tasmania, Hobart, Tas, Australia
[3] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10021 USA
[4] Yale Univ, Sch Med, Dept Gen Surg Pediat Surg, New Haven, CT 06520 USA
[5] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06510 USA
关键词
EWSR1-CREB3L1; fusion; low-grade fibromyxoid sarcoma; pediatric; renal; SCLEROSING EPITHELIOID FIBROSARCOMA; CLINICOPATHOLOGICAL ANALYSIS; MOLECULAR ANALYSIS; TUMOR;
D O I
10.2350/14-05-1487-CR.1
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
We present the case of a 6-year-old boy with a deceptively bland spindle cell renal neoplasm found to harbor the EWSR1-CREB3L1 gene fusion. This fusion has recently been described as a variant translocation in low-grade fibromyxoid sarcoma (LGFMS), a tumor more typically characterized by a recurrent t(7;16) chromosomal translocation, resulting in the fusion of FUS and CREB3L2 genes. LGFMS is an indolent tumor with late metastatic potential and a propensity for long-term disease recurrence. The tumor is rare in children, with only 33 published cases. In the pediatric population, it has not previously been reported arising in the kidney.
引用
收藏
页码:321 / 326
页数:6
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