Results 41 to 50 of about 460 (115)
Case Reports in Gastroenterology, 2020 Cronkhite-Canada syndrome (CCS) is a rare disease characterized by diffuse gastrointestinal polyposis with chronic diarrhea and ectodermal change, but its etiology is unknown.
Kazumoto Murata +5 more
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Intussusception in Cronkhite–Canada Syndrome
DiagnosticsCronkhite–Canada syndrome is a rare, non-hereditary polyposis syndrome characterized by non-specific gastrointestinal symptoms accompanied by alopecia, cutaneous hyperpigmentation, and nail dystrophy.
Li Ma, Ji Li, Xiaoyin Bai, Qingli Zhu
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Characteristics of Adult Intussusception due to Malignancy in Japanese Patients
JGH Open, Volume 9, Issue 2, February 2025.ABSTRACT Aims Adult intussusception (AI) is often associated with organic diseases. However, few studies have examined the causes of AI in Japanese patients. This study aimed to elucidate the clinical characteristics of AI due to malignancy in Japanese patients.
Shogo Kitahata +24 more
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A case of Cronkhite-Canada syndrome
Pifu-xingbing zhenliaoxue zazhiA case of Cronkhite-Canada syndrome is reported. A 68-year-old man presented with stomachache and diarrhea for 3 months. The dermatological examination revealed diffuse hair thinning, especially on the frontal region, symmetrical distribution of brown ...
Jiuxiang HUANG, Linlin SHI
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Cronkhite-Canada Syndrome: A Case Report and Review of Literature
Gastroenterology Research and Practice, 2009 Cronkhite-Canada syndrome (CCS) is a rare syndrome first described in 1955. (1) Since then, 400 cases worldwide have been reported in the literature.
Kevin T. Kao +2 more
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Organoids in gastrointestinal diseases: from bench to clinic
MedComm, Volume 5, Issue 7, July 2024.The established long‐term in vitro organoids models that have been derived from different gut segments, health status, ages, and species. Organoids models derived from different sources demonstrate distinct morphological and gene expression patterns. Abstract The etiology of gastrointestinal (GI) diseases is intricate and multifactorial, encompassing ...
Qinying Wang +6 more
wiley +1 more source
BMC Gastroenterology, 2019 Background Cronkhite-Canada syndrome is a rare disease of unknown etiology and the optimal treatment for this syndrome is unknown. Case presentation We present the case of a man who at the age of 66.0 years was diagnosed with Cronkhite-Canada syndrome ...
Sigrid Schulte +7 more
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Indian Journal of Dermatology, 1997 A case of Cronkhite- Canada syndrome in a 59 year old male is reported. The patient presented with generalized hyper pigmentation, alopecia, loss of finger and toenails, diarrhoea, weight loss and gastro- intestinal polyposis.
Narendra +3 more
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Cronkhite-Canada综合征诊疗的中国专家共识意见(2025年，北京)
罕见病研究Cronkhite-Canada综合征(Cronkhite-Canada syndrome，CCS)是一种以胃肠道多发息肉和外胚层改变为特征的罕见非遗传性疾病。其病因尚不明确，缺乏诊断的金标准，并发消化道肿瘤风险高于一般人群，早期诊断较为困难，疾病容易复发，需长期随访。中国罕见病联盟/北京罕见病诊疗与保障学会消化病学分会联合中华医学会消化病学分会罕见病协作组制定该共识，旨在对CCS的发病机制、临床表现、诊断及治疗给予相应的建议。
中国罕见病联盟/北京罕见病诊疗与保障学会消化病学分会 +1 more
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Successful surgical treatment of Cronkhite-Canada Syndrome with bilateral flail chest: a case report
BMC Surgery, 2020 Background Development of multiple rib fractures leading to bilateral flail chest in Cronkhite–Canada Syndrome (CCS) has not been reported. Case presentation A 59-year-old man presented with complaints of fatigue, chest pain, respiratory distress and ...
Guang-chao Lv +6 more
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