Department of Diagnostic Pathology, Shimada Municipal Hospital, Shizuoka, Japan.
Department of Gastroenterology, Shimada Municipal Hospital, Shizuoka, Japan.
Pathol Int. 2020 Oct;70(10):752-760. doi: 10.1111/pin.12996. Epub 2020 Aug 6.
Microscopic colitis (MC), encompassing collagenous colitis and lymphocytic colitis, is featured by chronic diarrhea, normal-looking endoscopic findings and unique microscopic appearance. After reviewing biopsied nonspecific colitis, we propose the third type of MC: colitis nucleomigrans (CN). Histopathological criteria of CN included: (i) chained nuclear migration to the middle part of the surface-lining columnar epithelium; (ii) apoptotic nuclear debris scattered below the nuclei; and (iii) mild/moderate chronic inflammation in the lamina propria. Thirty-three patients (M:F = 20:13; median age 63 years, range 17-88) fulfilled our criteria. Seven cases demonstrated MC-like clinical/endoscopic features. Mucosal reddening with or without erosion/aphtha was endoscopically observed in the remaining 26 cases with inflammatory bowel disease (IBD)-like features: occult/gross hematochezia seen in 19, abdominal pain in two and mucin secretion in two. Cleaved caspase-3-immunoreactive apoptotic debris appeared more frequently in IBD-like CN than in MC-like CN, while CD8-positive intraepithelial lymphocytes comparably appeared in both. Proton pump inhibitors (PPIs) were administered in five (71%) cases with MC-like features, and in three diarrhea improved after drug cessation. In IBD-like CN cases, eight (31%) received PPIs. Four patients received chemotherapy against malignancies. Four patients associated immune-related disorders. Microscopic appearance of CN also appeared in a remission state of ulcerative colitis (12/20 lesions).
显微镜结肠炎(MC)包括胶原性结肠炎和淋巴细胞性结肠炎,其特征为慢性腹泻、内镜检查正常和独特的显微镜下表现。在复查非特异性结肠炎活检后,我们提出了第三种 MC:核迁移性结肠炎(CN)。CN 的组织病理学标准包括:(i)核向表面衬里柱状上皮中部的链式迁移;(ii)凋亡核碎片散布在核下;和(iii)固有层轻度/中度慢性炎症。33 名患者(男/女=20:13;中位年龄 63 岁,范围 17-88 岁)符合我们的标准。7 例表现出 MC 样临床/内镜特征。在其余 26 例具有 IBD 样特征的病例中观察到黏膜发红伴或不伴糜烂/口疮:19 例有隐血/肉眼血便,2 例有腹痛,2 例有粘蛋白分泌。在 IBD 样 CN 中,cleaved caspase-3 免疫反应性凋亡碎片比 MC 样 CN 更常见,而 CD8 阳性上皮内淋巴细胞在两者中出现的频率相当。在具有 MC 样特征的 5 例(71%)中给予质子泵抑制剂(PPIs),在药物停止后 3 例腹泻改善。在 IBD 样 CN 病例中,8 例(31%)接受了 PPI 治疗。4 例患者接受了针对恶性肿瘤的化疗。4 例患者与免疫相关疾病有关。CN 的显微镜下表现也出现在溃疡性结肠炎(20 个病变中的 12 个)的缓解期。