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本文引用的文献

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Peutz-Jeghers syndrome: a systematic review and recommendations for management.佩吉特-杰格斯综合征:系统评价及管理建议。
Gut. 2010 Jul;59(7):975-86. doi: 10.1136/gut.2009.198499.
2
Cecal intussusception in an adult with Cronkhite-Canada syndrome relieved by colonoscopy.结肠镜检查缓解成年克朗凯特-加拿大综合征患者的盲肠套叠
Intern Med. 2010;49(12):1123-6. doi: 10.2169/internalmedicine.49.2813. Epub 2010 Jun 15.
3
Gardner's syndrome (familial adenomatous polyposis): a cilia-related disorder.加德纳综合征(家族性腺瘤性息肉病):一种与纤毛相关的疾病。
Lancet Oncol. 2009 Jul;10(7):727-35. doi: 10.1016/S1470-2045(09)70167-6.
4
A case of Cronkhite-Canada syndrome: remission after treatment with anti-Helicobacter pylori regimen.一例加拿大克朗凯特综合征:采用抗幽门螺杆菌疗法治疗后病情缓解。
Digestion. 2008;78(2-3):82-7. doi: 10.1159/000165354. Epub 2008 Oct 24.
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Hamartomatous polyposis syndromes.错构瘤性息肉病综合征
Surg Clin North Am. 2008 Aug;88(4):779-817, vii. doi: 10.1016/j.suc.2008.05.002.
6
[A Case of Cronkhite-Canada syndrome showing resolution with Helicobacter pylori eradication and omeprazole].[一例经根除幽门螺杆菌及使用奥美拉唑后病情缓解的克朗凯特-加拿大综合征病例]
Korean J Gastroenterol. 2006 Jan;47(1):59-64.
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A review of juvenile polyposis syndrome.青少年息肉病综合征综述。
J Gastroenterol Hepatol. 2005 Nov;20(11):1634-40. doi: 10.1111/j.1440-1746.2005.03865.x.
8
Cronkhite-Canada syndrome containing colon cancer and serrated adenoma lesions.伴有结肠癌和锯齿状腺瘤病变的克朗凯特-加拿大综合征
Digestion. 2004;69(1):57-62. doi: 10.1159/000076560. Epub 2004 Jan 30.
9
Generalized gastrointestinal polyposis; an unusual syndrome of polyposis, pigmentation, alopecia and onychotrophia.全身性胃肠道息肉病;一种伴有息肉病、色素沉着、脱发和甲营养障碍的罕见综合征。
N Engl J Med. 1955 Jun 16;252(24):1011-5. doi: 10.1056/NEJM195506162522401.
10
Cronkhite-Canada syndrome: sustained remission after corticosteroid treatment.克朗凯特-加拿大综合征:皮质类固醇治疗后持续缓解
Am J Gastroenterol. 2003 Jun;98(6):1444-6. doi: 10.1111/j.1572-0241.2003.07509.x.

腹泻、体重减轻和息肉病:考虑克朗凯特-加拿大综合征。

Diarrhoea, weight loss and polyposis: think Cronkhite-Canada syndrome.

作者信息

Aoun Elie, Victain Michelle, Mitre Marcia C

机构信息

Department of Internal Medicine, Division of Gastroenterology, Hepatology and Nutrition, West Penn Allegheny Health System, Pittsburgh, Pennsylvania, United States.

出版信息

BMJ Case Rep. 2011 Sep 19;2011:bcr0820114640. doi: 10.1136/bcr.08.2011.4640.

DOI:10.1136/bcr.08.2011.4640
PMID:22679262
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3185448/
Abstract

A 71-year-old male presented with nausea, diarrhoea and weight loss. He had mild to moderate alopecia, paucity of eyebrow hair, erythematous non-pruritic nodular rash on the wrists, toenail onychomychosis and scalp hyperpigmentation. A colonoscopy revealed an irregular, haemorrhagic 5 cm rectosigmoid mass. Biopsies revealed mucin distended glands and focal ischemic changes. A CT scan showed numerous polypoid-like lesions in the stomach. Upper endoscopy showed mucosal erythema and nodularity with polypoid-like lesions. Biopsies showed cystic glandular dilatation, lamina propria oedema and chronic inflammation consistent with Cronkhite-Canada syndrome (CCS). The patient was started on nutrition supplementation. His skin manifestations were treated topically and with mineral supplements. He improved within 10 weeks and is currently asymptomatic. A high index of suspicion for CCS should exist in patients who present with weight loss, diarrhoea and polyposis. If diagnosed early, the disease can be treated with the goal of clinical remission.

摘要

一名71岁男性出现恶心、腹泻和体重减轻症状。他有轻度至中度脱发、眉毛稀少、手腕上有红斑性非瘙痒性结节性皮疹、趾甲甲癣和头皮色素沉着。结肠镜检查发现乙状结肠直肠交界处有一个5厘米的不规则出血性肿块。活检显示粘蛋白扩张的腺体和局灶性缺血改变。CT扫描显示胃内有许多息肉样病变。上消化道内镜检查显示黏膜红斑和结节,伴有息肉样病变。活检显示囊性腺体扩张、固有层水肿和慢性炎症,符合克朗凯特-加拿大综合征(CCS)。患者开始接受营养补充。他的皮肤表现采用局部治疗和补充矿物质的方法。他在10周内有所改善,目前无症状。对于出现体重减轻、腹泻和息肉病的患者,应高度怀疑CCS。如果早期诊断,该疾病可以通过临床缓解为目标进行治疗。