临床健康犬和慢性腹泻犬经口小肠活检的组织学表现。

I van der Gaag, R P Happé
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引用次数: 0

摘要

对临床健康对照犬17只,慢性腹泻犬383只,共400只犬进行小肠吸钳活检2024例的组织学调查。3.5%的抽吸活检和22.6%的钳活检不适合检查,9只狗无法诊断,0.4%的狗存在胃窦粘膜。活检可从近三分之一的小肠进行。在17只对照犬中描述了正常组织学,包括平均绒毛长度、标准偏差和范围。给出了犬类肠炎的分类。55只慢性腹泻犬出现绒毛萎缩,无肠炎;51只狗有中度绒毛萎缩,4只狗有重度绒毛萎缩。93只犬出现绒毛萎缩合并肠炎,其中淋巴细胞-浆细胞性肠炎57只,嗜酸性肠炎14只,卡他性肠炎6只,溃疡性肠炎4只,淋巴细胞-浆细胞性和嗜酸性合并肠炎11只,淋巴细胞-浆细胞性和卡他性合并肠炎1只。50只犬无绒毛萎缩性肠炎:淋巴细胞浆细胞性肠炎39只,嗜酸性粒细胞性肠炎4只,卡他性肠炎2只,化脓性(微脓肿)1只,淋巴细胞浆细胞性和嗜酸性粒细胞性肠炎合并3只,局灶性坏死1只。12只狗表现出淋巴肉瘤,另外8只狗被诊断为淋巴肉瘤和/或肠炎。发现1例癌。其他表现为出血、水肿、糜烂、绒毛肌肉肥大、上皮内淋巴细胞数量增加或减少、杯状细胞数量增加或减少、淋巴管扩张、隐窝囊肿、隐窝脓肿和胃化生。一些品种,如德国牧羊犬、佛兰德斯猎犬、西班牙猎犬、柯利牧羊犬、大丹犬和猎犬,似乎比其他品种更容易患绒毛萎缩和肠炎。嗜酸性肠炎在德国牧羊犬、杜宾犬和罗威纳犬中也有轻微流行。轻度绒毛萎缩主要见于0-4岁的狗,而严重的绒毛萎缩见于4岁以上的狗。进一步的品种,年龄或性别倾向无法找到。该方法对小肠近端弥漫性粘膜病变特别有用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The histological appearance of peroral small intestinal biopsies in clinically healthy dogs and dogs with chronic diarrhea.

A survey of the histology of 2,024 small intestinal suction and forceps biopsies in 400 dogs, consisting of 17 clinically healthy control dogs and 383 dogs with chronic diarrhea is presented. Three and a half percent of the suction biopsies and 22.6 percent of the forceps biopsies were unsuitable for examination, making a diagnosis impossible in 9 dogs, and in 0.4 percent antral mucosa was present. Biopsies could be obtained from the proximal one third of the small intestine. The normal histology, including mean villous length, its standard deviation and its range is described in the 17 control dogs. A classification of enteritis in dogs is given. Villous atrophy without enteritis was found in 55 dogs with chronic diarrhea; 51 dogs had moderate and four severe villous atrophy. Villous atrophy combined with enteritis was found in 93 dogs, 57 of which had lymphocytic-plasmacytic enteritis, 14 had eosinophilic enteritis, six catarrhal, four ulcerative, 11 a combination of lymphocytic-plasmacytic and eosinophilic enteritis and one dog had a combination of lymphocytic-plasmacytic and catarrhal enteritis. Enteritis without villous atrophy was found in 50 dogs: 39 had lymphocytic-plasmacytic enteritis, four eosinophilic, two catarrhal, one purulent (microabscesses), three a combination of lymphocytic-plasmacytic and eosinophilic enteritis and one dog had focal necrosis. Twelve dogs showed a lymphosarcoma and in eight other dogs a differential diagnosis of lymphosarcoma and/or enteritis was made. One carcinoma was found. Other findings were hemorrhages, oedema, erosions, muscular hypertrophy in the villi, an increased or decreased number of intraepithelial lymphocytes, an increased or decreased number of goblet cells, lymphangiectasia, crypt cysts, crypt abscesses and gastric metaplasia. Some breeds, such as the German Shepherd dog, Bouvier des Flandres, Spaniel, Collie, Great Dane and Retriever appear to be more susceptible than other breeds for villous atrophy and enteritis. A slight prevalence of the German Shepherd dog, Doberman Pinscher and Rottweiler was also observed for eosinophilic enteritis. Mild villous atrophy is mostly found in dogs aged 0-4 years, whereas severe villous atrophy is found in dogs older than 4 years. Further breed, age or sex predisposition could not be found. The method appears especially useful for diffuse mucosal lesions of the proximal small intestine.

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