...
首页> 外文期刊>BMC Gastroenterology >Cronkhite-Canada syndrome: a rare case report and literature review
【24h】

Cronkhite-Canada syndrome: a rare case report and literature review

机译:Cronkhite-Canada综合征:罕见病例报告和文献复习

获取原文

摘要

Background Cronkhite-Canada Syndrome (CCS) is a rare non-inherited disease characterized by gastrointestinal polyposis and ectodermal abnormalities, the estimated incidence is about one per million. Recognizing and curing the disorder face great challenge. Case presentation This report refers to a Chinese 52 year old man with gastrointestinal symptoms and ectodermal abnormalities. Gastrointestinal symptoms occurred without obvious cause, followed by ectodermal abnormalities after two months. In several hospitals, endoscopy examinations found numerous polypoid lesions in various sizes spreading over the stomach and the entire colon and rectum, histopathological examinations showed inflammatory and adenomatous polyp. In our hospital, both endoscopy and the contrast-enhanced computed tomography (CT) of small intestine showed gastrointestinal polyposis. Gastric antrum and the colon biopsy samples suggested hyperplastic and inflammatory polyp respectively. Endoscopic ultrasonography (EUS) suggested gastric wall thickening. Fujinnon intelligent color enhancement (FICE) revealed that the size of gastric glands pit varied, and vessels were visible. Confocal endoscope showed increased glandular epithelium layers. Magnifying narrow-band imaging endoscopy (ME-NBI) detected that pit pattern in the mucous of the polyp were regular and type III-IV of microvessels were seen. Biochemical investigations showed anemia, hypoalbuminemia and electrolyte disturbance. IgG, IgA and C3 decreased. Anti-ribosomal phosphoprotein is weak positive. The patient was given nutritional support treatment. Gstrointestinal symptoms and hyperpigmentation improved gradually. Conclusion The patient was ever hospitalized in four hospitals and was diagnosed with CCS after 8 months of gastrointestinal symptoms. So when encountering the patient with gastrointestinal polyposis and ectodermal abnormalities, try to take CCS into consideration. Due to its low incidence, no standard therapy regimen has been established so far. However, nutritional support treatment is of great significance.
机译:背景Cronkhite-Canada综合征(CCS)是一种罕见的非遗传性疾病,其特征是胃肠道息肉病和表皮异常,估计发病率约为百万分之一。识别和治愈该疾病面临巨大挑战。病例报告该报告是指一名52岁的中国人,有胃肠道症状和外胚层异常。发生胃肠道症状无明显原因,两个月后出现外胚层异常。在几家医院,内窥镜检查发现许多大小不等的息肉样病变分布在胃,整个结肠和直肠,组织病理学检查显示有炎症性腺瘤性息肉。在我们医院,内窥镜检查和小肠造影增强CT(CT)均显示胃肠道息肉病。胃窦和结肠活检标本分别提示增生性息肉和炎性息肉。内镜超声检查(EUS)提示胃壁增厚。藤农智能增色(FICE)显示胃腺坑的大小各不相同,并且可见血管。共聚焦内窥镜显示腺上皮层增加。放大的窄带成像内窥镜检查(ME-NBI)检测到息肉粘液中的凹坑模式是规则的,并且看到了微血管的III-IV型。生化检查显示贫血,低白蛋白血症和电解质紊乱。 IgG,IgA和C3降低。抗核糖体磷蛋白呈弱阳性。患者接受了营养支持治疗。胃肠道症状和色素沉着逐渐改善。结论该患者曾在四家医院住院,并在出现胃肠道症状8个月后被诊断为CCS。因此,当遇到胃肠道息肉病和外胚层异常的患者时,请尝试考虑CCS。由于其发病率低,迄今为止尚未建立标准的治疗方案。但是,营养支持治疗具有重要意义。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号