RBPMS-NTRK3融合基因阳性的腹膜后婴儿型纤维肉瘤1例
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青岛大学附属医院儿童血液肿瘤科,山东青岛 266000

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周心毅,男,硕士研究生。Email:zxy9949@163.com。

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A case report of retroperitoneal infantile fibrosarcoma with RBPMS-NTRK3 fusion gene positivity
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Department of Pediatric Hematology and Oncology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, China

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    摘要:

    患儿,女,3月龄,因哭闹不止3 d入院。检查发现腹膜后巨大肿块,生长迅速,难以手术切除,肿块穿刺活检病理诊断为婴儿型纤维肉瘤。先给予长春新碱-放线菌素D-环磷酰胺方案化疗,效果不佳。婴儿型纤维肉瘤常见突变为ETV6-NTRK3基因融合,通过二代基因组测序技术检出该患儿为RBPMS-NTRK3基因融合,为国内首例该突变婴儿型纤维肉瘤患者,使用拉罗替尼治疗后,肿块明显缩小。

    Abstract:

    A 3-month-old female infant was admitted for incessant crying for 3 days. Examination revealed a rapidly growing massive retroperitoneal mass that was difficult to resect. Needle biopsy confirmed infantile fibrosarcoma. Initial chemotherapy with the VAC regimen (vincristine, actinomycin D, and cyclophosphamide) was administered, but the response was poor. The common fusion in infantile fibrosarcoma is ETV6-NTRK3, and next-generation sequencing detected an RBPMS-NTRK3 gene fusion in this patient. To our knowledge, this is the first reported case of infantile fibrosarcoma with RBPMS-NTRK3 fusion in China. Treatment with larotrectinib resulted in marked tumor shrinkage.

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周心毅,姜健,王玲珍,郭峻宏.RBPMS-NTRK3融合基因阳性的腹膜后婴儿型纤维肉瘤1例[J].中国当代儿科杂志,2025,(12):1544-1548

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  • 收稿日期:2025-03-21
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  • 在线发布日期: 2026-01-26
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