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嗜酸粒细胞性胃肠炎的临床谱向黏膜病型转变。

A shift in the clinical spectrum of eosinophilic gastroenteritis toward the mucosal disease type.

机构信息

Enteric NeuroScience Program, Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, Minnesota 55905, USA.

出版信息

Clin Gastroenterol Hepatol. 2010 Aug;8(8):669-75; quiz e88. doi: 10.1016/j.cgh.2010.04.022. Epub 2010 May 6.

Abstract

BACKGROUND & AIMS: Eosinophilic gastroenteritis (EG) is a rare disorder characterized by eosinophilic infiltration of the gastrointestinal (GI) tract. Despite the increasing prevalence of eosinophilic GI disorders, the epidemiology of EG has not been well studied. We evaluated the clinical spectrum of EG.

METHODS

We reviewed data from patients diagnosed with EG, allergic gastroenteropathy, or eosinophilia and referred to gastroenterologists from 1987 to 2007 (n = 59; 52 with mucosal, 3 with muscularis, and 4 with subserosal disease). The study included subjects diagnosed with EG and those with a history that suggested EG, defined by GI symptoms; eosinophilic infiltration of the GI tract, eosinophilic ascites, or characteristic radiographic findings with eosinophilia; and no parasitic or extraintestinal disease. Findings were compared with those from patients with unexplained GI symptoms and peripheral eosinophilia (n = 11).

RESULTS

Associations between clinical variables and EG subgroups did not differ between patients with EG and peripheral eosinophilia. Fifty percent of patients with EG who underwent food allergy testing had a positive test result; only 32% of those with EG who underwent radiographic imaging had positive test results. Patients with EG received steroid therapy; 75% with mucosal, 67% with muscle, and 100% with subserosal disease received prednisone. Eighty-eight percent of patients who received only steroids (mean follow-up period, 7 mo) and 94% of patients who received steroids in combination with another therapy (mean follow-up period, 4 mo) had improved or resolved disease.

CONCLUSIONS

Unlike eosinophilic esophagitis, EG is rare. Results from this large study suggest that EG disease type has shifted toward that of the mucosal layer.

摘要

背景与目的

嗜酸性粒细胞性胃肠炎(EG)是一种罕见的疾病,其特征为胃肠道(GI)嗜酸性粒细胞浸润。尽管嗜酸性粒细胞性胃肠道疾病的患病率不断增加,但 EG 的流行病学尚未得到很好的研究。我们评估了 EG 的临床谱。

方法

我们回顾了 1987 年至 2007 年间被诊断为 EG、过敏性胃肠病或嗜酸性粒细胞增多症并转介给胃肠病学家的患者的数据(n=59;52 例黏膜,3 例肌层,4 例浆膜下疾病)。该研究包括诊断为 EG 的患者和有 GI 症状、GI 道嗜酸性粒细胞浸润、嗜酸性腹水或特征性放射影像学表现伴嗜酸性粒细胞增多、无寄生虫或肠外疾病的患者。将这些发现与不明原因的 GI 症状和外周嗜酸性粒细胞增多症患者(n=11)的发现进行比较。

结果

在 EG 患者和外周嗜酸性粒细胞增多症患者中,临床变量与 EG 亚组之间的相关性没有差异。接受食物过敏测试的 EG 患者中有 50%的测试结果为阳性;仅 32%的 EG 患者接受影像学检查的结果为阳性。接受类固醇治疗的 EG 患者;黏膜层 75%,肌层 67%,浆膜下 100%接受泼尼松治疗。仅接受类固醇治疗的患者中,88%(平均随访期为 7 个月)和接受类固醇联合其他治疗的患者中,94%(平均随访期为 4 个月)的疾病得到改善或缓解。

结论

与嗜酸性粒细胞性食管炎不同,EG 较为罕见。这项大型研究的结果表明,EG 疾病类型已向黏膜层转变。

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