ISSN 1004-4140
    CN 11-3017/P

    不同亚型胰腺浆液性囊腺瘤影像学特征及病理基础

    Imaging characteristics and differences among different pancreatic serous cystic neoplasm subtypes and pathological basis

    • 摘要:
      目的 探讨胰腺浆液性囊腺瘤(SCN)不同亚型的影像学特征及其病理学基础,提升术前诊断准确性。
      方法 回顾性分析65例经病理确诊的胰腺SCN患者的影像学及病理资料,依据形态学特征(囊腔大小)将其分为大囊型、微囊型、混合型和实质型四类,对比各亚型的CT/MRI影像特征差异,并与其病理组织学表现进行对照研究。
      结果 患者在年龄、病灶部位、临床表现及基础疾病方面无统计学差异。各亚型在密度及强化程度上存在统计学差异。SCN均表现为T2加权成像(T2WI)高信号、胰管无沟通、无转移征象,其他影像学共性特征包括分叶状轮廓及多发囊腔结构,其中内部钙化(CT)为SCN特异性表现但发生率偏低(28.3%)。大囊型SCN缺乏中央纤维瘢痕,微囊型及混合型SCN中央纤维瘢痕MRI显示率较高(63.2%)。实质型体积较小,呈显著均匀强化。病理学分析显示:大囊型囊腔间质薄且血管稀疏;微囊型富含纤维瘢痕组织;混合型兼具大囊与微囊特征;实质型以高血管密度和致密纤维基质为特征,微囊结构常规影像难分辨。
      结论 胰腺SCN各亚型具有特征性影像表现,影像表现与病理具有良好对应关系,结合病理与多模态影像可提升诊断准确性。

       

      Abstract: Objective To investigate the imaging characteristics and differences among pancreatic serous cystic neoplasm (SCN) subtypes and their pathological basis, aiming to improve preoperative diagnostic accuracy. Methods Imaging and pathological data of 65 patients with pathologically confirmed pancreatic SCN were analyzed retrospectively. The lesions were categorized into four subtypes based on morphological features: macrocystic, microcystic, mixed, and solid. Computed tomography/magnetic resonance imaging (CT/MRI) imaging features of each subtype were compared and correlated with histopathological findings. Results No statistically significant differences were observed among the age, lesion location, clinical manifestations, or comorbidities of subtypes (P > 0.05). Significant differences were observed in lesion density and enhancement patterns (P < 0.05). All SCN exhibited hyperintensity on T2-weighted imaging, absence of communication with the pancreatic duct, and no metastatic signs. In addition, other shared imaging features included lobulated contours and multicystic structures, with internal calcifications (on CT) being a specific but less frequent finding (28.3%). Macrocystic SCN lacked central scars, while microcystic and mixed subtypes displayed higher MRI detection rates of central fibrous scars (63.2%). Solid-type SCN were smaller in size, demonstrating marked homogeneous enhancement. Pathological analysis revealed: macrocystic SCN had thin stroma and sparse vasculature between cysts; microcystic SCN were rich in fibrous scar tissue; mixed-type combined features of both; solid-type SCN were characterized by high vascular density and dense fibrous stroma, with microcystic structures undetectable by conventional imaging. Conclusion Each pancreatic SCN subtype exhibited characteristic imaging features, and these imaging findings correlate well with pathological characteristics. A thorough understanding of their pathological basis, combined with multimodal imaging techniques, can significantly enhance the accuracy of imaging diagnosis.

       

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