Gofrit Ofer N, Yutkin Vladimir, Duvdevani Mordechai, Hidas Guy, Neuman Tzahi
Department of Urology, Hadassah Hebrew University Hospital, Jerusalem, Israel.
Department of Pathology, Hadassah Hebrew University Hospital, Jerusalem, Israel.
Histol Histopathol. 2025 Apr;40(4):477-483. doi: 10.14670/HH-18-817. Epub 2024 Sep 19.
The lamina propria (LP) of the urinary bladder lies between the urothelial mucosa and the muscularis propria. This complex stratum is composed of extracellular matrix, several cell types, and collagen types I and III fibers. LP invasion by urothelial carcinoma (progression from stage Ta to T1) is a determinant of bladder cancer advancement. We attempted to characterize collagen fiber arrangement in the LP. This could enrich our understanding of this important layer and potentially provide clues for sub-staging of the T1 bladder cancer. A total of 24 Masson trichrome-stained images of normal bladder, including 12,530 collagen fibers were quantitatively analyzed using the Dragonfly software. The LP was divided according to fiber orientation into superficial LP (SLP, 15% of the thickness) and the deep LP (DLP, 85% of the thickness). Collagen fiber geometry analysis demonstrated that the SLP fibers are more parallel to the urothelium with an average angle of 26±23 compared to 40±26 in the DLP (p=3.4x10), more packed (average distance to the closest fiber of 0.61±0.67 compared to 0.66±0.77, p=0.0001), and their aspect ratio is considerably longer (average of 1.93±0.12 compared to 0.20±0.11, p=2.84x10). No difference was found in fiber perimeter or Feret diameter. Thus, we conclude that bladder collagen fibers are arranged in two distinct layers: a dense-ordered SLP and a loose disorder DLP. This indicates that the physical barrier to cancer cell invasion probably lies in the SLP, immediately underneath the urothelium. Once this barrier is breached, the looser and disorganized DLP poses no remarkable obstacle. Thus, we believe that histology-based subdivisions of stage T1 are expected to fail in providing clinically meaningful prognostic information.
膀胱的固有层(LP)位于尿路上皮黏膜和固有肌层之间。这个复杂的层次由细胞外基质、几种细胞类型以及I型和III型胶原纤维组成。尿路上皮癌侵犯固有层(从Ta期进展到T1期)是膀胱癌进展的一个决定因素。我们试图描述固有层中胶原纤维的排列情况。这可以丰富我们对这一重要层次的理解,并有可能为T1期膀胱癌的亚分期提供线索。使用蜻蜓软件对总共24张正常膀胱的马松三色染色图像进行了定量分析,其中包括12530根胶原纤维。固有层根据纤维方向分为浅固有层(SLP,厚度的15%)和深固有层(DLP,厚度的85%)。胶原纤维几何分析表明,浅固有层的纤维与尿路上皮更平行,平均角度为26±23度,而深固有层为40±26度(p = 3.4×10),排列更紧密(与最近纤维的平均距离为0.61±0.67,而深固有层为0.66±0.77,p = 0.0001),且其长宽比长得多(平均为1.93±0.12,而深固有层为0.20±0.11,p = 2.84×10)。在纤维周长或费雷特直径方面未发现差异。因此,我们得出结论,膀胱胶原纤维排列成两个不同的层次:一个致密有序的浅固有层和一个疏松无序的深固有层。这表明癌细胞侵袭的物理屏障可能位于紧邻尿路上皮下方的浅固有层。一旦这个屏障被突破,更疏松且无序的深固有层不会构成显著障碍。因此,我们认为基于组织学的T1期细分预计无法提供具有临床意义的预后信息。