Surgical Outcome of Brunner's Gland Hamartoma: A Single-Centre Experience.

Pub Date : 2022-01-17 eCollection Date: 2022-01-01 DOI:10.1055/s-0041-1741510
Arkadeep Dhali, Sukanta Ray, Tuhin S Mandal, Somak Das, Ranajoy Ghosh, Sujan Khamrui, Gopal K Dhali, Avik Sarkar
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引用次数: 3

Abstract

Introduction  Brunner's gland hamartomas (BGH) are rare benign lesions with an incidence of <0.01%, accounting for 5 to 10% of all benign tumors of the duodenum. It requires expeditious management by a multidisciplinary team. The aim of the study is to report our experience with surgery for BGH. Methodology  Data of all patients who underwent surgical intervention for duodenal polypoidal mass between August 2007 and March 2020 were retrieved from our prospectively maintained gastrointestinal (GI) surgery database. All patients whose histopathology report of the resected specimen confirmed BGH ( n  = 9) were included in the present study. Other pathological diagnosis like duodenal lipoma ( n  = 2), ganglioneuroma ( n  = 1), adenoma ( n  = 10), and adenocarcinoma ( n  = 4) were excluded. Results  Nine patients had confirmatory histopathological diagnosis of BGH and met our inclusion criteria. Three (33.3%) of them were men with a median age of 45 (range: 24-61) years. The median interval between onset of symptoms and diagnosis of duodenal polyp was 14 (range: 4-180) days. Five patients (55.5%) presented with upper GI hemorrhage. Three (33.3%) patients presented with abdominal pain, and one (11.1%) patient presented with episodes of bilious vomiting. Diagnostic endoscopy could detect the lesion in all (100%) patients. Contrast-enhanced computed tomography detected duodenal polypoidal lesion in five (55.5%) patients. The mean size of tumor was 4.78 ± 1.36 cm. These lesions were symptomatic in all the patients and warranted intervention. In view of failed endoscopic intervention ( n  = 7, 77.7%), or extramural extension of the tumor ( n  = 2, 22.2%), surgical intervention was considered. Most commonly performed operation was duodenal polypectomy ( n  = 6, 66.6%). Three postoperative complications developed in two (22.2%) patients. There was no surgery-related mortality. After a median follow-up of 60 (12 -78) months, no patient developed GI bleed or intestinal obstruction. Conclusion  In this study, the clinical profile of BGH was explored from the surgeon's point of view. Although endoscopic management is the first-line treatment, surgery plays an important role, particularly, if this fails or is not feasible. In experienced hand, surgery can be performed with acceptable perioperative morbidity and mortality and long-term satisfactory outcomes.

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布伦纳腺错构瘤的手术结果:单中心经验。
Brunner’s gland错构瘤(BGH)是一种罕见的良性病变,其发病率为:2007年8月至2020年3月期间,所有接受十二指肠息肉样肿块手术干预的患者的数据均来自我们前瞻性维护的胃肠道(GI)手术数据库。所有切除标本的组织病理学报告证实为BGH的患者(n = 9)均纳入本研究。其他病理诊断如十二指肠脂肪瘤(n = 2)、神经节神经瘤(n = 1)、腺瘤(n = 10)和腺癌(n = 4)被排除。结果9例患者经组织病理学确诊为BGH,符合纳入标准。其中3例(33.3%)为男性,中位年龄为45岁(范围24-61岁)。从症状出现到诊断为十二指肠息肉的中位时间间隔为14天(范围4-180天)。5例(55.5%)患者表现为上消化道出血。3例(33.3%)患者出现腹痛,1例(11.1%)患者出现胆汁性呕吐。诊断性内窥镜检查均可检出病变(100%)。5例(55.5%)患者经增强计算机断层扫描发现十二指肠息肉样病变。肿瘤平均大小为4.78±1.36 cm。这些病变在所有患者中都有症状,需要干预。鉴于内镜干预失败(n = 7, 77.7%)或肿瘤向外扩展(n = 2, 22.2%),考虑手术干预。最常见的手术是十二指肠息肉切除术(n = 6, 66.6%)。2例(22.2%)患者出现3例术后并发症。没有手术相关的死亡率。中位随访60(12 -78)个月后,没有患者出现胃肠道出血或肠梗阻。结论本研究从外科医生的角度探讨了BGH的临床特征。虽然内窥镜治疗是一线治疗,但手术也起着重要作用,特别是在手术失败或不可行的情况下。在经验丰富的人手中,手术可以接受围手术期的发病率和死亡率和长期满意的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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