A Rare Case of Signet Ring Cell Carcinoma Arising on Duodenal Brunner’s Gland Hyperplasia Successfully Treated Via Endoscopic Resection

Hae Rin Lee, B. Lee, Kyung Bin Kim, Gwang Ha Kim, M. Lee, Dong Chan Joo
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Abstract

Signet-ring cell carcinoma (SRCC) is a rare tumor that most commonly occurs in the stomach. Duodenal SRCCs are extremely uncommon and account for approximately 1% of duodenal adenocarcinomas. Although Brunner’s gland hyperplasia (BGH) is a benign duodenal condition, studies have reported several cases of adenocarcinoma originating in an area of BGH. We report a rare case of early-stage SRCC originating in an area of BGH that was successfully treated using endoscopic mucosal resection. Based on the mucin phenotype observed in this case, it is reasonable to conclude that SRCC originated from gastric metaplasia in the area of BGH. Although BGH is a benign condition, careful evaluation is warranted for early detection of combined neoplasms.
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一例罕见的十二指肠布鲁纳氏腺增生引发的印戒细胞癌,经内镜下切除术成功治愈
信号环细胞癌(SRCC)是一种罕见的肿瘤,最常见于胃部。十二指肠 SRCC 极其罕见,约占十二指肠腺癌的 1%。虽然布鲁纳氏腺增生(BGH)是一种良性十二指肠疾病,但有研究报告了几例起源于布鲁纳氏腺增生区域的腺癌。我们报告了一例罕见的起源于BGH区域的早期SRCC病例,该病例采用内镜粘膜切除术成功治疗。根据在该病例中观察到的粘蛋白表型,可以合理地断定SRCC起源于BGH区域的胃化生。尽管BGH是一种良性病变,但仍应仔细评估,以便及早发现合并肿瘤。
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审稿时长
18 weeks
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