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人类免疫缺陷病毒感染患者周围型肺肿块的临床与超声造影特征分析

Clinical and contrast-enhanced ultrasonographic characteristics of peripheral lung masses in patients infected with human immunodeficiency virus

  • 摘要:
    目的 探讨人类免疫缺陷病毒(HIV)感染患者周围型肺肿块(peripheral lung mass, PLM)的临床特征及超声造影(CEUS)对PLM良恶性的诊断价值。
    方法 回顾性分析上海市公共卫生临床中心2020年1月至2023年12月收治的69例PLM患者的临床资料。所有患者均接受经皮穿刺活检,良性36例、恶性33例;HIV阳性25例、阴性44例。比较各组的临床特征及CEUS参数。
    结果 恶性肿块患者年龄大于良性肿块患者(P<0.05)。HIV阴性患者恶性肿块最大径大于HIV阳性患者(P<0.05);HIV阳性患者良恶性肿块最大径差异无统计学意义。19例患者行CEUS检查。HIV阳性(n=10)和阴性(n=9)患者恶性肿块(n=10)的CEUS表现多为边界模糊、延迟增强、增强不均匀及延迟达峰。良性肿块(n=9)的增强达峰时间早于恶性肿块(P<0.01),良恶性肿块增强开始和减退时间差异无统计学意义。HIV阳性患者中,5例良性肿块CEUS诊断与病理诊断结果不一致。
    结论 良恶性PLM患者的临床特征和CEUS参数有差异;CEUS对于HIV阳性患者PLM的良恶性鉴别价值较低,仍需依赖病理诊断。

     

    Abstract:
    Objective To evaluate the clinical characteristics of human immunodeficiency virus (HIV) infected patients with peripheral lung masses (PLMs), and to assess the diagnostic utility of contrast-enhanced ultrasound (CEUS) in differentiating benign and malignant PLMs.
    Methods A retrospective analysis was performed on the clinical data of 69 patients with PLM treated in Shanghai Public Health Clinical Center from January 2020 to December 2023. All patients underwent percutaneous biopsy, and were categorized into benign group (n=36) and malignant group (n=33). 25 patients were HIV-positive and 44 patients were HIV-negative. The clinical features and CEUS parameters in patients were compared across these groups.
    Results Patients with malignant masses were significantly older than those with benign masses (P<0.05). In the malignant group, HIV-negative patients exhibited significantly larger tumor diameters compared to HIV-positive patients (P<0.05); in the HIV-positive patients, no significant difference in tumor size was observed between benign and malignant masses. 19 patients underwent CEUS. 10 malignant masses, irrespective of HIV status (10 positive and 9 negative), commonly presented with indistinct margins, delayed enhancement, heterogeneous perfusion, and delayed peak enhancement on CEUS. 9 benign masses showed earlier peak enhancement compared to 10 malignant masses (P<0.05); no significant differences were observed in the initiation and washout time of enhancement between benign and malignant masses. In HIV-positive patients, 5 benign masses frequently demonstrated discrepancies between CEUS findings and pathological results.
    Conclusions The clinical and CEUS characteristics were different between benign and malignant PLMs. However, CEUS shows limited accuracy in distinguishing benign and malignant PLMs, underscoring the need for pathological confirmation.

     

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