A case of primary duodenal Brunner's gland hamartoma that gradually underwent morphological changes over a period of 10 years

IF 1.4 Q4 GASTROENTEROLOGY & HEPATOLOGY DEN open Pub Date : 2024-10-29 DOI:10.1002/deo2.70028
Yusuke Sunada, Hiromichi Yamane, Nobuaki Ochi, Hirohito Kirishi, Takako Saitou, Masafumi Miura, Hidekazu Nakanishi, Hideyo Fujiwara, Nagio Takigawa
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Abstract

Brunner's gland hamartoma (BGH) is a benign tumor occurring in the duodenal bulb. BGH is typically asymptomatic, but it has been shown to occasionally cause anemia.

The patient was a 76-year-old male. In October 2011, he was diagnosed with prostate cancer with multiple bone metastases and was referred to us for the treatment and examination of anemia. Hormonal therapy with androgen receptor antagonists and bisphosphonate administration following orchiectomy improved his symptoms. In August 2012, esophagogastroduodenoscopy (EGD) was performed due to stomach discomfort, revealing a 5 mm semi-pedunculated polyp in the duodenal bulb, Yamada-Fukutomi classification type II. Over the next 5 years, the prostate cancer treatment proceeded smoothly, and no endoscopic follow-up was conducted. In January 2017, during a health checkup, EGD revealed that the polyp in the duodenum bulb had changed morphologically with a distinct stalk measuring 10 mm. As there were no symptoms and only minimal tumor growth, a watchful waiting approach was adopted. In April 2022, due to the rapid progression of anemia, EGD was performed again, showing that the pedunculated polyp had enlarged to 20 mm in maximum diameter with an eroded surface and a stalk extending to 40 mm. Given the tumor enlargement and further examination of anemia, an endoscopic polypectomy was performed in May 2022. Histopathological examination confirmed the diagnosis of BGH. We observed a case of primary duodenal BGH during treatment for advanced prostate cancer, with endoscopic monitoring over 10 years. The morphological changes of BGH were clearly documented via EGD.

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一例原发性十二指肠布鲁氏腺瘤,10 年间逐渐发生形态变化。
布鲁氏腺瘤(BGH)是一种发生在十二指肠球部的良性肿瘤。BGH通常没有症状,但偶尔也会导致贫血。患者是一名76岁的男性。2011年10月,他被诊断出患有前列腺癌并伴有多处骨转移,转诊至我院接受治疗和贫血检查。使用雄激素受体拮抗剂进行激素治疗,并在睾丸切除术后服用双膦酸盐,改善了他的症状。2012 年 8 月,由于胃部不适,他接受了食管胃十二指肠镜检查(EGD),发现十二指肠球部有一个 5 毫米的半截状息肉,属于 Yamada-Fukutomi 分型 II 型。此后 5 年,前列腺癌治疗进展顺利,未进行内镜随访。2017 年 1 月,在一次健康检查中,胃肠镜检查发现十二指肠球部的息肉形态发生了变化,出现了 10 毫米长的明显息肉蒂。由于没有任何症状,肿瘤生长也很小,因此采取了观察等待的方法。2022 年 4 月,由于贫血的迅速发展,患者再次接受了胃肠造影检查,结果显示有蒂息肉的最大直径已扩大到 20 毫米,表面已被侵蚀,蒂部延伸到 40 毫米。鉴于肿瘤增大和贫血的进一步检查,2022 年 5 月,患者接受了内镜下息肉切除术。组织病理学检查确诊为 BGH。我们在治疗晚期前列腺癌期间观察到一例原发性十二指肠 BGH 病例,对其进行了长达 10 年的内镜监测。通过胃肠道造影,我们清楚地记录了BGH的形态变化。
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