Meyer Hans-Jonas, Potratz Johann, Jechorek Dörthe, Schramm Kai Ina, Borggrefe Jan, Surov Alexey
Department of Diagnostic and Interventional Radiology, University of Leipzig, Leipzig, Germany.
Department of Pathology, Otto von Guericke University, Magdeburg, Germany.
Dig Dis. 2025;43(1):46-53. doi: 10.1159/000540958. Epub 2024 Oct 21.
The relationships between histopathology and imaging remain elusive, and investigating the underlying reasons for tumor microstructure leading to an imaging phenotype is of clinical importance. In the present study, a cross-sectional guided biopsy specimen was used to correlate prebioptic magnetic resonance imaging (MRI) with immunohistochemical staining of the histopathologic specimen using precise spatial biopsy localization.
Twenty-seven patients with mass-forming cholangiocarcinoma (CCA) were included in the present analysis. All patients were imaged with a 1.5 T clinical scanner at least 1 month prior to biopsy. The contrast-enhanced dynamic sequences were analyzed with quantified signal intensities. The bioptic specimens were obtained by cross-sectional guided biopsy and further analyzed for cell density, proliferation index (Ki67), tumor-infiltrating lymphocytes, tumor-stroma ratio (TSR), and collagen.
There were no statistically significant correlations between MRI signal intensities and cell count, TSR, Ki67 index, and CD45 count. Only a moderate correlation was observed between relative signal intensities of the venous phase and the collagen-stained area (r = 0.40, p = 0.04).
DCE-MRI is not associated with histopathological features in CCA. The complex interactions of tumor and tumor microenvironment are not reflected in the MRI phenotype.
组织病理学与影像学之间的关系仍不明确,探究导致影像学表现的肿瘤微观结构的潜在原因具有临床重要性。在本研究中,使用横断面引导活检标本,通过精确的空间活检定位,将活检前磁共振成像(MRI)与组织病理标本的免疫组织化学染色相关联。
本分析纳入了27例肿块型胆管癌(CCA)患者。所有患者在活检前至少1个月使用1.5T临床扫描仪进行成像。对对比增强动态序列进行定量信号强度分析。通过横断面引导活检获取活检标本,并进一步分析细胞密度、增殖指数(Ki67)、肿瘤浸润淋巴细胞、肿瘤-基质比(TSR)和胶原蛋白。
MRI信号强度与细胞计数、TSR、Ki67指数和CD45计数之间无统计学显著相关性。仅在静脉期相对信号强度与胶原蛋白染色区域之间观察到中度相关性(r = 0.40,p = 0.04)。
动态对比增强MRI与CCA的组织病理学特征无关。肿瘤与肿瘤微环境的复杂相互作用未在MRI表型中体现。