Lorenz R, Gulotta U, Becker K, Bottermann P, Vogel G E, Classen M
Z Gastroenterol. 1986 Feb;24(2):85-92.
We report about a 76 years old patient with Cronkhite-Canada syndrome. The diagnosis has been found with the following clinical symptoms: diarrhea, anorexia, alopecia, and onychotrophia. Laboratory values: severe hypoproteinemia (total serum protein 4.3 g/dl, albumin 2.4 g/dl); endoscopical and radiological findings: a generalized polyposis which involved the whole intestine except the oesophagus. As far as we saw in our literature-overview of 55 patients with Cronkhite-Canada syndrome, this patient had for the first time a carcinoma of the urinary bladder and a Bricker operation 17 years before the onset of his disease. Further we remarked a lack in the resorption of the enterally administered thyroidal hormones. The progress was fatal despite a parenteral hyperalimentation and a treatment with antibiotics and glucocorticoids.
我们报告了一位76岁患有克朗凯特-加拿大综合征的患者。通过以下临床症状确诊:腹泻、厌食、脱发和甲营养不良。实验室检查值:严重低蛋白血症(血清总蛋白4.3g/dl,白蛋白2.4g/dl);内镜和放射学检查结果:广泛性息肉病,累及除食管外的整个肠道。据我们对55例克朗凯特-加拿大综合征患者的文献综述所见,该患者在疾病发作前17年首次出现膀胱癌并接受了布里克手术。此外,我们还注意到患者对肠内给予的甲状腺激素吸收不良。尽管进行了胃肠外高营养以及抗生素和糖皮质激素治疗,病情仍发展至致命结局。