| 词条 | Brunner's glands |
| 释义 |
| Name = Brunner's glands | Latin = glandulae duodenales | Image = gray1058.png | Caption = Section of duodenum. (Duodenal glands in submucosa are labeled at right, fourth from the top.) | Image2 = | Caption2 = | Location = Duodenum | System = Digestive system }} Brunner's glands (or duodenal glands) are compound tubular submucosal glands found in that portion of the duodenum which is above the hepatopancreatic sphincter (a.k.a. sphincter of Oddi). The main function of these glands is to produce a mucus-rich alkaline secretion i.e. Mucous (containing bicarbonate) in order to:
They also secrete epidermal growth factor, which inhibits parietal and chief cells of the stomach from secreting acid and their digestive enzymes.[1]{{citation needed|date=May 2015}} This is another form of protection for the duodenum. They are the distinguishing feature of the duodenum, and are named for the Swiss physician who first described them, Johann Conrad Brunner. StructureMicroanatomyThe duodenum is readily distinguished from other regions of the small intestine by the presence of submucosal Brunner's glands, which may pack the submucosa so completely that the typical submucosal connective tissue is obscured.{{citation needed|date=May 2018}} FunctionThe Brunner glands, which empty into the intestinal glands, secrete an alkaline fluid composed of mucin, which exerts a physiologic anti-acid function by coating the duodenal epithelium, therefore protecting it from the acid chyme of the stomach. Furthermore, in response to the presence of acid in the duodenum, these glands secrete pepsinogen and urogastrone, which inhibit gastric acid secretion.{{citation needed|date=May 2014}} The main function of these glands is to produce a mucus-rich alkaline secretion (containing bicarbonate) in order to:
Clinical significanceHyperplasia of Brunner glands with a lesion greater than 1 cm was initially described as a Brunner gland adenoma. Several features of these lesions favor their designation as hamartomas, including the lack of encapsulation; the mixture of acini, smooth muscles, adipose tissue, Paneth cells, and mucosal glands; and the lack of any cell atypia. These hamartomas are rare, with approximately 150 cases described in the literature.6 It is estimated that they represent approximately 5-10% of benign duodenal tumors. They are variable in size, typically 1–3 cm, with only a few reported cases of lesions larger than 5 cm. Most patients with Brunner gland hamartomas are asymptomatic or have nonspecific complaints such as nausea, bloating, or vague abdominal pain. Most reports in the literature describe local surgical resection of Brunner gland hamartoma via duodenotomy. Increasingly, successful endoscopic resection has been reported and is primarily used for pedunculated Brunner gland hamartomas. The endoscopic approach in selective cases appears to be safe, less invasive, and less costly.{{citation needed|date=May 2018}} See alsoPeutz-Jeghers syndromeReferences1. ^{{Cite journal|last=Gregory|first=H.|last2=Preston|first2=B. M.|date=1977-01-01|title=The primary structure of human urogastrone|journal=International Journal of Peptide and Protein Research|volume=9|issue=2|pages=107–118|issn=0367-8377|pmid=300079}} External links
1 : Digestive system |
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