Brunneroma: Unusual Case of Gastroduodenal Intussusception

H. Kumar, A. Heroor, Arul Vanan
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Abstract

Introduction: Brunner organ hamartoma, otherwise called brunneroma, is a rare benign tumor of the duodenum. These benign tumors can be asymptomatic or can present with obstructive manifestations as well as gastrointestinal bleeding. Intussusception is an uncommon introduction for a brunneroma. ). The distribution of Brunner’s gland hamartomas is duodenal bulb (57%), the second (27%) and third (5%) portions of the duodenum, the pyloric channel (5%), jejunum (2%), and proximal ileum (2%). Case Report: A 55 year old female came to the gastrointestinal surgery division with complain of epigastric pain intermittent, and aggravated by eating food and associated with nonbilious, non-projectile. There was no history of hematemesis, melena, jaundice, weight loss, or anorexia. Radiological investigations were suggestive of gastric outlet obstruction. The patient underwent a distal gastrectomy . A diagnosis of Brunner’s gland adenoma was made on histopathological examination. Conclusion: Our case was unique as an uncommon tumor Brunner's organ hamartoma, rare location: pyloric, around 8 cm, and rare clinical presentation of Gastroduodenal intussusception. In spite of the fact that brunneroma is an uncommon element, it ought to continuously be considered as a differential conclusion of duodenal polypoidal disease. Larger disease can cause Gastroduodenal intussusceptions and can display with obstructive indications. Keyword: Brunner gland hamartoma, Brunneroma, intussusception, obstruction.
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褐色神经瘤:胃十二指肠肠套叠的罕见病例
简介:布鲁纳器官错构瘤,又称布鲁纳神经瘤,是一种罕见的十二指肠良性肿瘤。这些良性肿瘤可无症状或表现为梗阻性表现以及胃肠道出血。肠套叠是褐色神经瘤的罕见病因。. 布伦纳腺错构瘤分布于十二指肠球部(57%)、十二指肠第二段(27%)和第三段(5%)、幽门通道(5%)、空肠(2%)和回肠近端(2%)。病例报告:一名55岁女性,主诉间歇性胃脘痛,因进食而加重,并伴有非胆汁性、非抛射性腹痛。无吐血、黑黑、黄疸、体重减轻或厌食史。影像学检查提示胃出口梗阻。病人接受了远端胃切除术。经组织病理学检查诊断为勃伦纳腺腺瘤。结论:我们的病例是一种罕见的肿瘤布鲁纳脏器错构瘤,罕见的位置:幽门,约8cm,罕见的临床表现为胃十二指肠肠套叠。尽管褐色神经瘤是一种罕见的因素,但它应继续被视为十二指肠息肉病的鉴别结论。较大的疾病可引起胃十二指肠肠套叠,并可表现为梗阻性指征。关键词:布鲁纳腺错构瘤,布鲁纳瘤,肠套叠,梗阻。
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