Kurella Ravi R, Ancha Hanumantha R, Hussain Sanam, Lightfoot Stan A, Harty Richard
Division of Gastroenterology, Department of Medicine, Oklahoma University Health Sciences Center, Oklahoma City, OK, USA.
South Med J. 2008 Jun;101(6):648-50. doi: 10.1097/SMJ.0b013e318172435a.
The pathogenesis of Brunner gland hamartoma of the duodenum is unknown. This case report describes the chronology of the development of Brunner gland hamartoma from Brunner gland hyperplasia over a 12-year interval. The study subject, a 64-year-old man with chronic iron deficiency anemia, underwent serial upper endoscopies during this period. Repeated endoscopies demonstrated the evolution of Brunner gland hyperplasia, as manifest endoscopically by a submucosal mass, to a pedunculated polyp with histologic features of Brunner gland hamartoma. The duodenal polypoid mass was removed by snare polypectomy. The patient also had a chronic Helicobacter pylori infection of the stomach. This report details the time-dependent evolution of Brunner gland hyperplasia to hamartoma in association with chronic gastric H. pylori infection.
十二指肠布伦纳腺错构瘤的发病机制尚不清楚。本病例报告描述了布伦纳腺错构瘤在12年时间里从布伦纳腺增生发展而来的过程。研究对象是一名64岁患有慢性缺铁性贫血的男性,在此期间接受了系列上消化道内镜检查。反复的内镜检查显示了布伦纳腺增生的演变过程,内镜下表现为黏膜下肿块,进而发展为带蒂息肉,具有布伦纳腺错构瘤的组织学特征。十二指肠息肉样肿块通过圈套息肉切除术切除。该患者还患有胃部慢性幽门螺杆菌感染。本报告详细阐述了布伦纳腺增生与慢性胃部幽门螺杆菌感染相关联向错构瘤的时间依赖性演变。