Eisenhower Health, Rancho Mirage, CA, USA.
University of California, Riverside, USA.
J Investig Med High Impact Case Rep. 2023 Jan-Dec;11:23247096231179451. doi: 10.1177/23247096231179451.
Cronkhite-Canada syndrome (CCS) is an acquired polyposis syndrome with gastrointestinal and extraintestinal manifestations. Given its rarity and lack of standard treatment, diagnosis and treatment are challenging. Steroid therapy and nutritional support are conventional treatments. There is no consensus on management of steroid-refractory cases. Here, we report the diagnosis and treatment course of a 54-year-old Asian male with CCS, whose initial treatment with prednisone 60 mg a day led to partial response and disease flare up during prednisone tapering. The use of infliximab and azathioprine led to promising remission of his symptoms.
Cronkhite-Canada 综合征(CCS)是一种获得性息肉病综合征,具有胃肠道和肠外表现。由于其罕见性和缺乏标准治疗,诊断和治疗具有挑战性。类固醇治疗和营养支持是常规治疗。对于类固醇难治性病例的治疗尚无共识。在这里,我们报告了一例 54 岁亚洲男性 CCS 的诊断和治疗过程,他最初每天接受泼尼松 60mg 的治疗导致部分缓解,在泼尼松逐渐减量期间疾病复发。使用英夫利昔单抗和硫唑嘌呤导致他的症状有了显著缓解。