Nguyen Long Cong, Vu Khanh Truong, Vo Trang Thi Thuy, Trinh Chau Ha, Do Tan Dang, Pham Ngoc Thi Van, Pham Tuyen Van, Nguyen Thanh Tuan, Nguyen Hiep Canh, Byeon Jeong-Sik
Gastroenterology and Hepatology Center, Bach Mai Hospital, Hanoi 10000, Viet Nam.
Radiology Center, Bach Mai Hospital, Hanoi 10000, Viet Nam.
World J Clin Cases. 2021 Nov 6;9(31):9670-9679. doi: 10.12998/wjcc.v9.i31.9670.
Brunner's gland hyperplasia (BGH) is a rare benign lesion of the duodenum. Lipomatous pseudohypertrophy (LiPH) of the pancreas is an extremely rare disease. Because each condition is rare, the probability of purely coincidental coexistence of both conditions is extremely low.
We report a 26-year-old man presenting to our hospital with symptoms of recurrent upper gastrointestinal bleeding. Upper gastrointestinal endoscopy showed a huge pedunculated polypoid lesion in the duodenum with bleeding at the base of the lesion. Histopathological examination of the duodenal biopsy specimens showed BGH. Besides, abdominal computed tomography and magnetic resonance imaging revealed marked fat replacement over the entire pancreas, confirmed by histopathological evaluation on percutaneous pancreatic biopsies. Based on the radiological and histological findings, LiPH of the pancreas and BGH were diagnosed. The patient refused any surgical intervention. Therefore, he was managed with supportive treatment. The patient's symptoms improved and there was no further bleeding.
This is the first well-documented case showing the coexistence of LiPH of the pancreas and BGH.
十二指肠Brunner腺增生(BGH)是一种罕见的十二指肠良性病变。胰腺脂肪性假肥大(LiPH)是一种极其罕见的疾病。由于每种情况都很罕见,两种情况单纯巧合并存的概率极低。
我们报告一名26岁男性因反复上消化道出血症状前来我院就诊。上消化道内镜检查显示十二指肠有一个巨大的带蒂息肉样病变,病变基部有出血。十二指肠活检标本的组织病理学检查显示为BGH。此外,腹部计算机断层扫描和磁共振成像显示整个胰腺有明显的脂肪替代,经经皮胰腺活检的组织病理学评估证实。根据影像学和组织学检查结果,诊断为胰腺LiPH和BGH。患者拒绝任何手术干预。因此,对其进行支持性治疗。患者症状改善,未再出血。
这是第一例有充分记录显示胰腺LiPH和BGH并存的病例。