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肿瘤相关性骨软化症。

Tumor-Induced Osteomalacia.

机构信息

Endocrinology Department, School of Medicine, Pontificia Universidad Católica de Chile, Av. Diagonal Paraguay 362, Cuarto piso, Santiago, Chile.

Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.

出版信息

Calcif Tissue Int. 2021 Jan;108(1):128-142. doi: 10.1007/s00223-020-00691-6. Epub 2020 Jun 5.

Abstract

Tumor-induced osteomalacia (TIO) is a rare paraneoplastic syndrome caused by tumoral production of fibroblast growth factor 23 (FGF23). The hallmark biochemical features include hypophosphatemia due to renal phosphate wasting, inappropriately normal or frankly low 1,25-dihydroxy-vitamin D, and inappropriately normal or elevated FGF23. TIO is caused by typically small, slow growing, benign phosphaturic mesenchymal tumors (PMTs) that are located almost anywhere in the body from the skull to the feet, in soft tissue or bone. The recent identification of fusion genes in a significant subset of PMTs has provided important insights into PMT tumorigenesis. Although management of this disease may seem straightforward, considering that complete resection of the tumor leads to its cure, locating these often-tiny tumors is frequently a challenge. For this purpose, a stepwise, systematic approach is required. It starts with thorough medical history and physical examination, followed by functional imaging, and confirmation of identified lesions by anatomical imaging. If the tumor resection is not possible, medical therapy with phosphate and active vitamin D is indicated. Novel therapeutic approaches include image-guided tumor ablation and medical treatment with the anti-FGF23 antibody burosumab or the pan-FGFR tyrosine kinase inhibitor, BGJ398/infigratinib. Great progress has been made in the diagnosis and treatment of TIO, and more is likely to come, turning this challenging, debilitating disease into a gratifying cure for patients and their providers.

摘要

肿瘤相关性骨软化症(TIO)是一种罕见的副瘤综合征,由肿瘤产生成纤维细胞生长因子 23(FGF23)引起。其典型的生化特征包括因肾脏排磷而导致的低磷血症、1,25-二羟维生素 D 水平不适当的正常或降低,以及 FGF23 水平不适当的正常或升高。TIO 由通常较小、生长缓慢的良性磷酸化解质肿瘤(PMT)引起,这些肿瘤几乎可以在身体的任何部位生长,从颅骨到足部,位于软组织或骨骼中。最近在相当一部分 PMT 中发现融合基因,为 PMT 的肿瘤发生提供了重要的见解。尽管这种疾病的治疗方法似乎很简单,因为肿瘤的完全切除可导致其治愈,但定位这些通常很小的肿瘤常常是一个挑战。为此,需要采用逐步、系统的方法。它从详细的病史和体格检查开始,然后进行功能成像,最后通过解剖成像确认已识别的病变。如果肿瘤无法切除,则需要进行磷酸盐和活性维生素 D 的药物治疗。新的治疗方法包括图像引导的肿瘤消融和使用抗 FGF23 抗体布罗昔单抗或泛 FGFR 酪氨酸激酶抑制剂 BGJ398/英菲格拉替尼进行药物治疗。在 TIO 的诊断和治疗方面已经取得了很大的进展,而且可能会有更多的进展,将这种具有挑战性、使人衰弱的疾病转变为患者及其治疗提供者的可喜治愈。

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