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首页> 外文期刊>Journal of Comparative Pathology >Small Intestinal Lymphatic Hypoplasia in Three Dogs with Clinical Signs of Protein-losing Enteropathy
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Small Intestinal Lymphatic Hypoplasia in Three Dogs with Clinical Signs of Protein-losing Enteropathy

机译:三只狗的小肠淋巴结性发育不全,蛋白失去肠病的临床症状

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摘要

Intestinal lymphatic hypoplasia (ILH) is a rare but well-documented cause of protein-losing enteropathy (PLE) in human infants. To our knowledge, this condition has not been reported previously in veterinary medicine. Here we report the clinical and histopathological findings in three dogs that presented with clinical signs of PLE. The onset of PLE was early in an 18-month-old Great Pyrenees, while the other two dogs, a pug and a Tibetan terrier, had a later onset at 4 and 12 years of age, respectively. The presence of intestinal lymphatic and blood vessels was assessed by immunohistochemistry for human prospero homeobox 1 (pros-1), a lymphatic endothelial nuclear transcription factor and human von Willebrand factor (vWf), a marker of vascular endothelial cells, respectively. Small intestinal specimens taken from each dog showed severe mucosal oedema with a lack of prox-1 labelling of villous lacteals, dilated and tortuous vWf immunoreactive villous arterial and capillary blood vessels, and variable lamina propria mixed inflammatory cell infiltrates. Other histological features of ILH included club-shaped villi that were lined by low cuboidal epithelium or epithelial cells with cytoplasmic pallor and microvacuolar change, extrusion zone epithelial inversion and thin and inconspicuous villous longitudinal smooth muscles. While ILH is an uncommon diagnosis, it should be considered as a differential in dogs with clinical signs of PLE. The cause of canine ILH is unknown; however, a congenital abnormality with early or late onset of clinical signs is suspected. Diagnosis of ILH can be challenging; however, immunohistochemical labelling of lymphatic endothelial cells with pros-1 is essential for making this diagnosis. (C) 2018 Elsevier Ltd. All rights reserved.
机译:肠淋巴肿瘤发育不全(ILH)是人类婴儿中蛋白质失血肠病(PLE)的罕见但良好的。据我们所知,这种情况尚未在兽医中报告。在这里,我们在三只狗中报告了临床迹象的临床和组织病理学发现。 PLE的发作早期在一个18个月大的伟大的比利牛斯,而另外两只狗,哈巴狗和藏梗,分别在4至12岁时稍后发病。通过免疫组织化学对人繁华的Homeobox 1(PROS-1),淋巴内皮核转录因子和人von Willebrand因子(VWF),分别是血管内皮细胞的标志物评估肠道淋巴管和血管的存在。从每只狗采取的小肠样本均显示严重的粘膜水肿,缺乏绒毛唇裂,扩张和曲折的VWF免疫反应性绒毛动脉和毛细血管血管,以及可变的椎板混合炎症细胞浸润。 ILH的其他组织学特征包括俱乐部形绒毛,具有细胞质钙和微亚脱石的低立方体上皮或上皮细胞,挤出区上皮反转和薄且不显眼的绒毛纵向平滑肌。虽然ILH是一种罕见的诊断,但它应该被认为是患有PLE临床迹象的狗的差异。犬Ilh的原因是未知的;然而,怀疑临床症状早期或晚期的先天性异常。 ILH的诊断可能具有挑战性;然而,具有PROS-1的淋巴内皮细胞的免疫组织化学标记对于进行这种诊断至关重要。 (c)2018年elestvier有限公司保留所有权利。

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