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家族性腺瘤性息肉病中的胃腺瘤很常见,但很隐匿,且病程呈良性。

Gastric adenomas in familial adenomatous polyposis are common, but subtle, and have a benign course.

作者信息

Ngamruengphong Saowanee, Boardman Lisa A, Heigh Russell I, Krishna Murli, Roberts Maegan E, Riegert-Johnson Douglas L

机构信息

Division of Gastroenterology and Hepatology, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL 32224, USA.

出版信息

Hered Cancer Clin Pract. 2014 Feb 24;12(1):4. doi: 10.1186/1897-4287-12-4.

Abstract

BACKGROUND

Patients with familial adenomatous polyposis (FAP) are known to have an increased risk for gastric adenomas. The clinical features of gastric adenomas in FAP have not been well characterized, and there is a lack of standardized approaches to the management of these lesions.

AIMS

To study the endoscopic appearance, risk factors, clinical course, and response to therapy of gastric adenomas in patients with FAP.

METHODS

We retrospectively reviewed the records of 97 patients with FAP who underwent esophagogastroduodenoscopy (EGD) at Mayo Clinic (Florida, Rochester and Arizona) between 2004 and 2013.

RESULTS

Nine patients (9%) had biopsy-proven gastric adenomas. Adenomas were located in the antrum (five patients), in the body and fundus in the setting of background fundic gland polyps (FGP) (three patients), and in the body not associated with FGP (one patient). Adenoma size was 3-40 mm and the number of adenomas per patient ranged from one to 20. Adenomas in the antrum were flat and subtle, whereas those in the gastric body or fundus were polypoid and difficult to differentiate from the cystic FGPs seen in patients with FAP. The performing endoscopists reported difficulty with identifying adenomas, and six patients had at least one EGD within the previous three years where gastric adenomas were not reported. Adenomas were classified as tubular in eight patients and tubulovillous in one patient. High grade dysplasia was noted in one patient. After a median follow-up of 63 months (interquartile range: 20-149 months), no patient in our entire cohort (with or without gastric adenomas) developed gastric cancer. The patients in whom gastric adenoma developed, compared to those without gastric adenoma, were more likely to be younger [36 ± 12 vs. 48 ± 15 years, p = 0.02], have concomitant chronic gastritis [22% vs. 0%, p = 0.008], and have desmoid tumors [5 (56%) vs. 19 (22%), p = 0.04].

CONCLUSIONS

Gastric adenomas are not uncommon in patients with FAP and are often difficult to identify endoscopically. Endoscopists should have a high degree of suspicion for gastric adenomas in these patients and a low threshold to biopsy. Given the benign clinical course, recommended initial management is conservative with endoscopic therapy and periodic surveillance.

摘要

背景

已知家族性腺瘤性息肉病(FAP)患者患胃腺瘤的风险增加。FAP患者胃腺瘤的临床特征尚未得到充分描述,并且缺乏针对这些病变的标准化管理方法。

目的

研究FAP患者胃腺瘤的内镜表现、危险因素、临床病程及治疗反应。

方法

我们回顾性分析了2004年至2013年间在梅奥诊所(佛罗里达州、罗切斯特和亚利桑那州)接受食管胃十二指肠镜检查(EGD)的97例FAP患者的记录。

结果

9例(9%)患者经活检证实患有胃腺瘤。腺瘤位于胃窦(5例)、伴有胃底腺息肉(FGP)背景的胃体和胃底(3例)以及不伴有FGP的胃体(1例)。腺瘤大小为3 - 40毫米,每位患者的腺瘤数量为1至20个。胃窦部的腺瘤扁平且不明显,而胃体或胃底部的腺瘤呈息肉样,难以与FAP患者中见到的囊性FGP区分。实施内镜检查的医生报告识别腺瘤存在困难,6例患者在过去三年内至少接受过一次EGD检查,但未报告有胃腺瘤。8例患者的腺瘤被分类为管状,1例为管状绒毛状。1例患者存在高级别异型增生。中位随访63个月(四分位间距:20 - 149个月)后,我们整个队列(有或无胃腺瘤)中无患者发生胃癌。发生胃腺瘤的患者与未发生胃腺瘤的患者相比,更可能年龄较小[36 ± 12岁对48 ± 15岁,p = 0.02],伴有慢性胃炎[22%对0%,p = 0.008],以及患有硬纤维瘤[5例(56%)对19例(22%),p = 0.04]。

结论

胃腺瘤在FAP患者中并不少见,且在内镜下常难以识别。内镜医生应对这些患者的胃腺瘤保持高度怀疑,并降低活检阈值。鉴于临床病程良性,推荐的初始管理是采用内镜治疗和定期监测的保守方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/604c/3943270/2c9fe62e5877/1897-4287-12-4-1.jpg

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