Deasy J M, Steele G, Ross D S, Lahey S J, Wilson R E, Madara J
J Surg Oncol. 1983 Sep;24(1):36-40. doi: 10.1002/jso.2930240109.
Although gut-associated lymphoid tissue in the form of discrete lymphoid patches (LP-GALT) in mammalian intestine in most prominent in the distal ileum, appendix, and, in some species, the cecal appendage, LP-GALT can be found throughout the intestinal tract. LP-GALT appears as single or multiple subepithelial lymphoid follicles covered by a specialized, structurally unique epithelium. In the colon of the Wistar/Furth (W/Fu) rat, LP-GALT appears as aggregates of follicles, or lymphoid patches, that can be detected macroscopically. We studied the relationship between 1,2-dimethylhydrazine- (DMH) induced colon carcinomas and the lymphoid patch associated epithelium in these animals. In addition, we defined the normal distribution of colonic lymphoid patches in both DMH-treated and control rats. Patches were found macroscopically and confirmed by histologic examination at five constant sites: lower pole of cecum, proximal ascending colon, the major colonic flexure, mid descending colon, and the rectosigmoid. There are also the predominant sites of DMH induced carcinomas in W/Fu rats. In 120 DMH-treated animals, 109 colon carcinomas were found. Eight percent were in the lower pole of the cecum, 56% in the proximal ascending colon, 16% at the major flexure, 15% in the mid descending colon, and 5% in the rectosigmoid. Lymphoid patches could often be detected histologically in association with DMH-induced tumors. The depth of tumor invasion was found to correlate inversely with our ability to identify tumor-associated lymphoid patches suggesting that tumors arising at the anatomical sites were lymphoid patches occur progressively destroyed them. Of colon tumors confirmed histologically to be associated with lymphoid patches, 88% were superficial lesions confined to the submucosa and 12% were more extensive but confined to the bowel wall. No lymphoid patches could be found associated with tumors that extended through the bowel wall. Thus, DMH-induced colon carcinomas in W/Fu rats arise at sites containing preexisting LP-GALT with associated specialized epithelium.
尽管以离散淋巴样小结形式存在的肠道相关淋巴组织(LP-GALT)在哺乳动物肠道中最显著地存在于回肠末端、阑尾以及某些物种的盲肠附件中,但LP-GALT可在整个肠道中发现。LP-GALT表现为单个或多个被特殊的、结构独特的上皮覆盖的上皮下淋巴滤泡。在Wistar/Furth(W/Fu)大鼠的结肠中,LP-GALT表现为滤泡聚集体或淋巴样小结,可通过肉眼检测到。我们研究了1,2-二甲基肼(DMH)诱导的结肠癌与这些动物中淋巴样小结相关上皮之间的关系。此外,我们确定了DMH处理组和对照组大鼠结肠淋巴样小结的正常分布。通过肉眼发现小结,并在五个固定部位经组织学检查证实:盲肠下端、升结肠近端、结肠主曲、降结肠中部以及直肠乙状结肠部。这些也是W/Fu大鼠中DMH诱导的癌的主要发生部位。在120只经DMH处理的动物中,发现了109例结肠癌。8%位于盲肠下端,56%位于升结肠近端,16%位于主曲处,15%位于降结肠中部,5%位于直肠乙状结肠部。经组织学检查,淋巴样小结常与DMH诱导的肿瘤相关。发现肿瘤浸润深度与我们识别肿瘤相关淋巴样小结的能力呈负相关,这表明在淋巴样小结所在的解剖部位发生的肿瘤会逐渐破坏它们。在经组织学证实与淋巴样小结相关的结肠肿瘤中,88%为局限于黏膜下层的浅表病变,12%范围更广但局限于肠壁。未发现与穿透肠壁的肿瘤相关的淋巴样小结。因此,W/Fu大鼠中DMH诱导的结肠癌发生于含有预先存在的LP-GALT及相关特殊上皮的部位。