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一位腹腔疾病患者的小肠腺癌中存在 DDR2 突变。

A small bowel adenocarcinoma harboring a DDR2 mutation in a celiac patient.

机构信息

Medical Oncology Unit, Istituti Clinici Scientifici Maugeri IRCCS, Via Maugeri, 10 27100, Pavia, Italy.

Department of Internal Medicine and Therapeutics, University of Pavia, Pavia, Italy.

出版信息

Clin J Gastroenterol. 2024 Dec;17(6):1026-1032. doi: 10.1007/s12328-024-02025-7. Epub 2024 Aug 8.

Abstract

We present the case of a 62-year-old man with a history of celiac disease and IgA deficiency, following a strict gluten-free diet that was admitted to our hospital for recurrent abdominal pain, fatigue and melena. Esophagogastroduodenoscopy and colonoscopy with biopsies were normal. A video-capsule endoscopy was performed and revealed a sub-stenosing, vegetating, and bleeding lesion in the first jejunal loop. He underwent laparotomic surgery with resection of the involved segment with loco-regional lymphadenectomy. The pathological report described a poorly differentiated adenocarcinoma of the jejunum, stage IIIA (pT3pN1). Analysis of next-generation sequencing (NGS) of DNA on the surgical sample revealed a likely pathogenetic variant in exon 15 of the DDR2 gene (c.2003G > A) and a TP53 non-frame-shift deletion (c.585_602del). Considering the risk of recurrence, he was candidate to 6 months of adjuvant chemotherapy with platinum salt and fluoropyrimidine. Thirty-eight months after the diagnosis, the patient is still disease free and in good clinical condition. This is the first described case of SBA with DDR2 mutation. Considering the limited therapeutic options beyond surgery for SBA, molecular analyses could become promising for the search for potential targetable alterations for treatments with new available drugs.

摘要

我们报告了一例 62 岁男性病例,该患者患有乳糜泻和 IgA 缺乏症病史,遵循严格的无麸质饮食,因反复腹痛、乏力和黑便而入院。食管胃十二指肠镜和结肠镜检查并活检均正常。进行了视频胶囊内镜检查,显示在第一空肠环有一处狭窄、增生和出血性病变。他接受了剖腹手术,切除受累段并进行局部区域淋巴结清扫。病理报告描述了 IIIA 期(pT3pN1)的空肠低分化腺癌。对手术样本的下一代测序 (NGS) 分析显示 DDR2 基因外显子 15 中可能存在致病变异(c.2003G>A)和 TP53 无框移缺失(c.585_602del)。鉴于复发风险,他适合接受 6 个月的含铂盐和氟嘧啶的辅助化疗。诊断后 38 个月,患者仍无疾病且临床状况良好。这是首例 DDR2 基因突变的 SBA 描述病例。鉴于 SBA 除手术外治疗选择有限,分子分析可能成为寻找潜在可靶向改变以进行新的可用药物治疗的有前途的方法。

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