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拉罗替尼治疗伴有NTRK1基因融合的黄色肉芽肿:一例报告

Larotrectinib Treatment of Xanthogranuloma With NTRK1 Gene Fusion: A Case Report.

作者信息

Ralston Grace, Humeniuk Michael

机构信息

Internal Medicine, Edward Via College of Osteopathic Medicine, Spartanburg, USA.

Medical Oncology, Gibbs Cancer Center, Spartanburg Regional Healthcare System, Spartanburg, USA.

出版信息

Cureus. 2025 May 22;17(5):e84609. doi: 10.7759/cureus.84609. eCollection 2025 May.

Abstract

Non-Langerhans cell histiocytosis (NLCH) is a broad disorder encompassing different diseases arising from dermal dendritic histiocytes. Xanthogranuloma (XG) is a cutaneous subtype of NLCH that can be present in isolated or multiple locations. If localized, XGs can be treated with surgical resection or radiation; however, if they present more disseminated, they are poorly responsive to traditional chemotherapeutic agents. This case discusses a 26-year-old male who presented with diffuse light brown/tan papules progressively spreading from the bilateral groin axillae to the trunk, pelvis, and eyelids over the course of six months. Histologic evaluation demonstrated findings consistent with XG with immunostaining strongly positive for neurotrophic tyrosine kinase receptor 1 (NTRK1) gene fusion. He was diagnosed as likely having an early form of XG disseminatum before visceral involvement had developed, but given how rare and complex XG diseases are to classify, he might also be considered to have disseminated adult XG. He was started on larotrectinib, an oral tropomyosin inhibitor used to treat solid tumors associated with NTRK gene fusions. Improvement in the lesions was noticeable as early as six weeks, with a successful partial clinical response by four months of treatment, where he ceased to develop new lesions, and the pre-existing lesions became more macular. He eventually discontinued therapy due to a known side effect of weight gain and has continued to maintain his response since. This report demonstrates a positive clinical response of an NTRK1 inhibitor in an adult with NTRK1-positive XGs, providing further evidence that targeted therapy may be beneficial for these otherwise challenging patients.

摘要

非朗格汉斯细胞组织细胞增生症(NLCH)是一种广泛的疾病,涵盖了由皮肤树突状组织细胞引起的不同疾病。黄肉芽肿(XG)是NLCH的一种皮肤亚型,可出现在单个或多个部位。如果是局限性的,XG可以通过手术切除或放疗进行治疗;然而,如果它们表现为更广泛的分布,则对传统化疗药物反应不佳。本病例讨论了一名26岁男性,他在六个月的时间里出现了弥漫性浅棕色/棕褐色丘疹,从双侧腹股沟、腋窝逐渐蔓延至躯干、骨盆和眼睑。组织学评估显示结果与XG一致,免疫染色显示神经营养性酪氨酸激酶受体1(NTRK1)基因融合呈强阳性。他被诊断为可能患有早期播散性XG,尚未出现内脏受累,但考虑到XG疾病的分类非常罕见且复杂,他也可能被认为患有成人播散性XG。他开始使用拉罗替尼治疗,这是一种口服原肌球蛋白抑制剂,用于治疗与NTRK基因融合相关的实体瘤。早在六周时,病变就有明显改善,治疗四个月时临床部分缓解成功,即他不再出现新的病变,原有病变变得更呈斑片状。他最终因已知的体重增加副作用而停药,此后病情持续缓解。本报告证明了NTRK1抑制剂对一名患有NTRK1阳性XG的成年人有积极的临床反应,进一步证明靶向治疗可能对这些原本具有挑战性的患者有益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e5a/12182870/2c75077ee422/cureus-0017-00000084609-i01.jpg

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