Ono Yuho, Gonzalez Raul S
Department of Pathology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Department of Pathology and Laboratory Medicine, Emory University Hospital, 1364 Clifton Ave NE, Atlanta, GA, 30322, USA.
Virchows Arch. 2025 May 8. doi: 10.1007/s00428-025-04076-8.
The histologic distinction of segmental colitis associated with diverticulosis (SCAD) from inflammatory bowel disease (IBD) is difficult; however, distinguishing the two is important for patient management. This study aimed to examine histologic changes in SCAD and compare them to those in IBD. We retrospectively identified patients with highly likely SCAD and known IBD who were biopsied at our institution. With diagnosis blinded, H&E slides were reviewed for cryptitis, crypt abscesses, lamina propria (LP) neutrophils, erosion/ulceration, LP expansion by mononuclear cells, prominent basal lymphoid aggregates, basal lymphoplasmacytosis, crypt distortion, crypt dilation, granulomatous reaction to damaged crypts, increased intraepithelial lymphocytes, mucin depletion, Paneth cell metaplasia, LP smooth muscle wisps, and crypt rupture. Features between groups were compared by chi-squared analysis, with statistical significance set at P < 0.05. There were 81 SCAD cases (79% in the sigmoid colon) and 166 IBD cases. A separate cohort of 27 patients had both IBD and diverticulosis. Compared to the IBD cohort, the SCAD cohort was significantly less likely to demonstrate crypt abscesses (20% vs. 45%, P < 0.0001), prominent basal lymphoid aggregates (37% vs. 51%, P = 0.042), crypt distortion (7% vs. 25%, P = 0.00090), Paneth cell metaplasia (37% vs. 57%, P = 0.0061), and crypt rupture (1% vs. 11%, P = 0.0089). These histologic features, although not entirely specific, may be of value in distinguishing IBD from SCAD, particularly when clinical context is unclear or not readily available.
将与憩室病相关的节段性结肠炎(SCAD)与炎症性肠病(IBD)进行组织学区分很困难;然而,区分两者对患者管理很重要。本研究旨在检查SCAD的组织学变化,并将其与IBD的组织学变化进行比较。我们回顾性地确定了在我们机构接受活检的高度疑似SCAD和已知IBD的患者。在诊断不知情的情况下,对苏木精-伊红(H&E)染色切片进行隐窝炎、隐窝脓肿、固有层(LP)中性粒细胞、糜烂/溃疡、单核细胞引起的LP扩张、突出的基底淋巴样聚集、基底淋巴细胞浆细胞增多、隐窝扭曲、隐窝扩张、对受损隐窝的肉芽肿反应、上皮内淋巴细胞增多、粘蛋白减少、潘氏细胞化生、LP平滑肌束和隐窝破裂的检查。通过卡方分析比较两组之间的特征,统计学显著性设定为P < 0.05。有81例SCAD病例(79%位于乙状结肠)和166例IBD病例。另外一组27例患者同时患有IBD和憩室病。与IBD队列相比,SCAD队列出现隐窝脓肿(20%对45%,P < 0.0001)、突出的基底淋巴样聚集(37%对51%,P = 0.042)、隐窝扭曲(7%对25%,P = 0.00090)、潘氏细胞化生(37%对57%,P = 0.0061)和隐窝破裂(1%对11%,P = 0.0089)的可能性显著更低。这些组织学特征虽然并非完全特异,但在区分IBD和SCAD方面可能有价值,特别是在临床背景不明确或难以获取时。