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卡梅隆病变:一个仍被忽视的诊断。病例报告及文献系统回顾。

Cameron lesions: A still overlooked diagnosis. Case report and systematic review of literature.

机构信息

Gastroenterology Unit, 'Nuovo Regina Margherita' Hospital, Rome, Italy.

Digestive Endoscopy Unit, 'S. Agostino-Estense' Hospital, Modena, Italy.

出版信息

Clin Res Hepatol Gastroenterol. 2018 Dec;42(6):604-609. doi: 10.1016/j.clinre.2018.05.002. Epub 2018 Jun 14.

DOI:10.1016/j.clinre.2018.05.002
PMID:29910147
Abstract

Cameron lesions are erosive-ulcerative alterations of gastric mucosa occurring in patients with large hiatal hernia, potentially causing gastrointestinal bleeding and iron deficiency anaemia. Diagnosis may be challenging, and not infrequently erosions are overlooked at endoscopy, so that repeated and unnecessary diagnostic procedures are performed, particularly in those patients with chronic anaemia. We described two peculiar cases of patients with iron deficiency anaemia in whom Cameron lesions were either overlooked or misinterpreted. By reviewing data of 22publications reporting endoscopic and clinical data of 140patients, we noted a large prevalence of females (75%). The most frequent presenting symptoms were anaemia (62%) and overt gastrointestinal bleeding (36%). Noteworthy, as many as 69% of patients underwent one or more previous upper endoscopy before diagnosis of Cameron lesion was achieved. Patients were mainly treated with proton pump inhibitor (PPI) therapy and iron supplementation. Moreover, endoscopic haemostasis was performed in 10% of case, blood transfusion was required in one third of cases, and a similar quote of patients underwent a surgical approach for hiatal hernia repair. The observation that as many as 60% patients were already receiving standard PPI therapy when diagnosis was performed would suggest that either long-term treatment with adequate dose PPI or surgical approach for hiatal hernia repair is required. In conclusion, Cameron lesion is still an overlooked diagnosis in patients with iron deficiency anaemia in whom a 5-9.2% prevalence has been reported.

摘要

卡梅伦病变是胃黏膜的糜烂性溃疡改变,发生于巨大食管裂孔疝患者,可能导致胃肠道出血和缺铁性贫血。诊断可能具有挑战性,内镜检查时常会忽略溃疡,因此会进行重复且不必要的诊断程序,尤其是在那些患有慢性贫血的患者中。我们描述了两例特殊的缺铁性贫血患者病例,他们的卡梅伦病变要么被忽略,要么被误诊。通过回顾 22 篇报告了 140 例患者内镜和临床数据的文献资料,我们注意到女性的患病率很高(75%)。最常见的症状是贫血(62%)和显性胃肠道出血(36%)。值得注意的是,多达 69%的患者在诊断出卡梅伦病变之前,曾接受过一次或多次上消化道内镜检查。患者主要接受质子泵抑制剂(PPI)治疗和铁补充治疗。此外,10%的病例进行了内镜止血,三分之一的病例需要输血,类似比例的患者接受了食管裂孔疝修补的手术治疗。观察到多达 60%的患者在诊断时已经接受了标准的 PPI 治疗,这表明需要长期使用足够剂量的 PPI 进行治疗或进行食管裂孔疝修补的手术治疗。总之,在缺铁性贫血患者中,卡梅伦病变仍然是一个被忽视的诊断,其患病率为 5-9.2%。

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Clin Res Hepatol Gastroenterol. 2018 Dec;42(6):604-609. doi: 10.1016/j.clinre.2018.05.002. Epub 2018 Jun 14.
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