Suppr超能文献

克罗恩病并发小肠腺癌:单中心经验强调发育异常筛查的重要性。

Small bowel adenocarcinoma complicating Crohn's disease: a single-centre experience emphasizing the importance of screening for dysplasia.

作者信息

Grolleau Chloé, Pote Nicolas M, Guedj Nathalie S, Zappa Magaly, Theou-Anton Nathalie, Bouhnik Yoram, Panis Yves, Cazals-Hatem Dominique L

机构信息

Department of Pathology, AP-HP, Hôpital Beaujon, 92110, Clichy, France.

University Paris Diderot, Sorbonne Paris Cité, 75018, Paris, France.

出版信息

Virchows Arch. 2017 Nov;471(5):611-617. doi: 10.1007/s00428-017-2125-z. Epub 2017 Apr 18.

Abstract

Small bowel adenocarcinoma (SBA) complicating Crohn's disease (CD) is rare and generally found incidentally on surgical specimens. We report our experience in CD-associated SBA observed this last decade in a tertiary referral centre in order to update its incidence, clinical presentation and pathological features. All SBAs diagnosed in patients who underwent surgery for CD between 2006 and 2016 were retrospectively included. Clinico-pathological characteristics were reviewed, and follow-up was updated. SBA was diagnosed in 9 (1.7%) of 522 patients who underwent SB resection(s) after a median CD duration of 15 years [0-32]. The median age at diagnosis was 46 years. Seven (78%) patients had obstructive symptoms refractory to medical treatment. Pre-operative biopsy revealed neoplasia in five (56%) patients (dysplasia in three and SBA in two) justifying the surgery. Two (29%) of the seven patients with imaging had features suggestive of cancer. In all specimens, SBA developed in active ileitis with adjacent dysplasia. Stage I low-grade tubulo-glandular adenocarcinoma was observed in 33% of patients. Stage IV high-grade adenocarcinoma was observed in 56% of patients, and mucinous/signet ring cell differentiation predominated in 44% of patients. Molecular analysis showed no BRAF mutation, a KRAS mutation in one case and a microsatellite instability phenotype suggestive of Lynch syndrome in one case. After a median follow-up of 24 months [7-82], four (44%) patients died with advanced stage IV SBA. This surgical series confirms that CD-associated SBA is rare with an incidence of 1.7%. Adjacent dysplasia was present in all specimens and was identified before surgery in all patients who benefit from ileal biopsies. This strengthens the importance of screening all longstanding CD by endoscopy if surgery is not considered.

摘要

克罗恩病(CD)并发小肠腺癌(SBA)较为罕见,通常在手术标本中偶然发现。我们报告了过去十年在一家三级转诊中心观察到的CD相关SBA的经验,以更新其发病率、临床表现和病理特征。回顾性纳入了2006年至2016年间因CD接受手术的患者中诊断出的所有SBA。对临床病理特征进行了回顾,并更新了随访情况。522例接受小肠切除术的患者中,9例(1.7%)被诊断为SBA,CD病程中位数为15年[0 - 32年]。诊断时的中位年龄为46岁。7例(78%)患者有内科治疗无效的梗阻症状。术前活检显示5例(56%)患者有肿瘤形成(3例发育异常,2例SBA),这证明了手术的合理性。7例有影像学检查的患者中,2例(29%)有提示癌症的特征。在所有标本中,SBA均发生于活动性回肠炎伴相邻发育异常。33%的患者为I期低级别管状腺癌。56%的患者为IV期高级别腺癌,44%的患者以黏液/印戒细胞分化为主。分子分析显示无BRAF突变,1例有KRAS突变,1例有提示林奇综合征的微卫星不稳定性表型。中位随访24个月[7 - 82个月]后,4例(44%)患者死于IV期晚期SBA。该手术系列证实CD相关SBA罕见,发病率为1.7%。所有标本中均存在相邻发育异常,所有受益于回肠活检的患者在手术前均被发现。这强化了如果不考虑手术,通过内镜筛查所有长期CD患者的重要性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验