Clinical and imaging characteristics of phosphaturic mesenchymal tumors: a case series analysis.

IF 3.4 2区 医学 Q2 ONCOLOGY
Haifeng Hou, Xiaofeng Zhou, Lijun Zhang
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引用次数: 0

Abstract

Objective: To characterize the clinical, biochemical, pathological, and multimodal imaging features of phosphaturic mesenchymal tumors (PMTs).

Methods: We retrospectively reviewed 10 patients with pathologically confirmed PMT. Clinical presentation, laboratory findings, histopathologic and immunohistochemical features, and imaging manifestations across multiple modalities were systematically analyzed.

Results: All patients presented with long-standing fatigue and bone pain. Preoperative laboratory tests revealed varying degrees of hypophosphatemia and elevated alkaline phosphatase, while postoperative serum phosphate levels gradually normalized. Histopathology demonstrated heterogeneous morphologies. Immunohistochemistry showed consistent SATB2 and SSTR2 positivity in tested cases, whereas the Ki-67 proliferation index ranged from 1% to 15%. On CT, primary lesions appeared as soft-tissue density masses or ground-glass-like nodules, often with irregular calcification and focal bone destruction. MRI demonstrated hypointensity on T1-weighted images, hyperintensity on T2-weighted images, and moderate to marked heterogeneous enhancement. Both [18F]F-OC PET/CT and [18F]F-FDG PET/CT revealed variable degrees of radiotracer uptake in all lesions.

Conclusion: PMTs are characterized by typical TIO-related clinical and biochemical abnormalities, and SATB2 and SSTR2 are highly sensitive immunohistochemical markers for definitive diagnosis. Whole-body [18F]F-OC PET/CT, targeting somatostatin receptors, serves as a highly specific first-line modality for tumor localization. Dedicated CT and MRI provide essential anatomic characterization for surgical planning, while [18F]F-FDG PET/CT offers complementary, non-tumor-specific metabolic information. [99mTc]Tc-MDP planar bone scintigraphy is useful for assessing the systemic skeletal burden of osteomalacia. This stepwise, multimodal approach improves diagnostic accuracy and supports timely surgical management.

磷化间充质肿瘤的临床和影像学特征:一个病例系列分析。
目的:探讨磷质间充质瘤(pmt)的临床、生化、病理及多模态影像学特征。方法:回顾性分析10例经病理证实的PMT患者。系统分析临床表现、实验室结果、组织病理学和免疫组织化学特征以及多种形式的影像学表现。结果:所有患者均表现为长期疲劳和骨痛。术前实验室检查显示不同程度的低磷血症和碱性磷酸酶升高,而术后血清磷酸盐水平逐渐恢复正常。组织病理学显示形态不均匀。免疫组化显示SATB2和SSTR2在检测病例中一致阳性,而Ki-67增殖指数在1%至15%之间。CT表现为软组织密度肿块或磨玻璃样结节,常伴有不规则钙化和局灶性骨破坏。MRI显示t1加权图像低信号,t2加权图像高信号,中度至明显的不均匀增强。[18F]F-OC PET/CT和[18F]F-FDG PET/CT在所有病变中均显示不同程度的放射性示踪剂摄取。结论:pmt以典型的tio相关临床及生化异常为特征,SATB2和SSTR2是高度敏感的免疫组化标志物,可用于明确诊断。全身[18F]F-OC PET/CT靶向生长抑素受体,可作为肿瘤定位的高特异性一线方式。专用的CT和MRI为手术计划提供必要的解剖特征,而[18F]F-FDG PET/CT提供补充的非肿瘤特异性代谢信息。[99mTc]Tc-MDP平面骨显像可用于评估骨软化症的全身骨骼负荷。这种逐步的、多模式的方法提高了诊断的准确性,并支持及时的手术管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Cancer
BMC Cancer 医学-肿瘤学
CiteScore
6.00
自引率
2.60%
发文量
1204
审稿时长
6.8 months
期刊介绍: BMC Cancer is an open access, peer-reviewed journal that considers articles on all aspects of cancer research, including the pathophysiology, prevention, diagnosis and treatment of cancers. The journal welcomes submissions concerning molecular and cellular biology, genetics, epidemiology, and clinical trials.
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