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具有神经营养性酪氨酸受体激酶融合转录本的儿科肿瘤的影像学特征。

Imaging characterization of paediatric tumours with the neurotrophic tyrosine receptor kinase fusion transcript.

机构信息

Department of Imaging, Institut Curie, PSL University, Paris, 75005, France.

SIREDO Oncology Center (Care, Innovation and Research for Children and AYA with Cancer), Institut Curie, PSL University, Paris, 75005, France.

出版信息

Br J Radiol. 2024 Mar 28;97(1156):734-743. doi: 10.1093/bjr/tqae016.

Abstract

OBJECTIVES

The neurotrophic tyrosine receptor kinase (NTRK) fusion transcript (FT) is a major genetic landmark of infantile fibrosarcoma (IFS) and cellular congenital mesoblastic nephroma (cCMN) but is also described in other tumours. The recent availability of NTRK-targeted drugs enhances the need for better identification. We aimed to describe the anatomic locations and imaging features of tumours with NTRK-FT in children.

CASE SERIES

Imaging characteristics of NTRK-FT tumours of 41 children (median age: 4 months; 63% <1 year old; range: 0-188) managed between 2001 and 2019 were retrospectively analysed. The tumours were located in the soft tissues (n = 24, including 19 IFS), kidneys (n = 9, including 8 cCMN), central nervous system (CNS) (n = 5), lung (n = 2), and bone (n = 1). The tumours were frequently deep-located (93%) and heterogeneous (71%) with necrotic (53%) or haemorrhagic components (29%). Although inconstant, enlarged intratumoural vessels were a recurrent finding (70%) with an irregular distribution (63%) in the most frequent anatomical locations.

CONCLUSION

Paediatric NTRK-FT tumours mainly occur in infants with very variable histotypes and locations. Rich and irregular intra-tumoural vascularization are recurrent findings.

ADVANCES IN KNOWLEDGE

Apart from IFS of soft tissues and cCMN of the kidneys, others NTRK-FT tumours locations have to be known, as CNS tumours. Better knowledge of the imaging characteristics may help guide the pathological and biological identification.

摘要

目的

神经酪氨酸受体激酶(NTRK)融合转录本(FT)是婴儿纤维肉瘤(IFS)和细胞性先天性中胚层肾瘤(cCMN)的主要遗传标志,但也在其他肿瘤中描述过。最近出现的 NTRK 靶向药物增强了更好识别的需求。我们旨在描述儿童 NTRK-FT 肿瘤的解剖部位和影像学特征。

病例系列

回顾性分析了 2001 年至 2019 年间治疗的 41 名儿童(中位年龄:4 个月;63%<1 岁;范围:0-188)的 NTRK-FT 肿瘤的影像学特征。肿瘤位于软组织(n=24,包括 19 例 IFS)、肾脏(n=9,包括 8 例 cCMN)、中枢神经系统(CNS)(n=5)、肺(n=2)和骨(n=1)。肿瘤通常位于深部(93%)且不均匀(71%),伴有坏死(53%)或出血成分(29%)。尽管不常见,但增大的肿瘤内血管是一种反复出现的发现(70%),其分布不规则(63%),这是最常见的解剖部位。

结论

儿科 NTRK-FT 肿瘤主要发生在婴儿中,具有非常不同的组织学和位置。丰富且不规则的肿瘤内血管化是反复出现的发现。

知识的进步

除了软组织的 IFS 和肾脏的 cCMN 外,还必须了解其他 NTRK-FT 肿瘤的位置,包括 CNS 肿瘤。更好地了解影像学特征可能有助于指导病理和生物学鉴定。

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