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一例罕见的背侧胰腺完全缺如病例。

A Rare Case of Complete Agenesis of Dorsal Pancreas.

作者信息

Jain Atul, Singh Malwinder, Dey Subhajeet, Kaura Ankit, Diwakar Gaurav

机构信息

Department of Surgery, ESI Post Graduate Institute of Medical Sciences & Research, ESI Hospital, Basaidarapur, New Delhi, India.

出版信息

Euroasian J Hepatogastroenterol. 2017 Jul-Dec;7(2):183-184. doi: 10.5005/jp-journals-10018-1245. Epub 2017 Sep 29.

Abstract

Agenesis of dorsal pancreas (ADP) is an extremely rare congenital anomaly that results from defective development of pancreas. Most ADP patients are asymptomatic; if symptomatic, they present with epigastric pain. About half of affected individuals develop diabetes mellitus (DM), resulting from reduced islet cell mass secondary to the absence of endocrine structures. Being very rare, it is generally not kept in mind while dealing these cases and are not suspected until imaging investigations are not done. In our case study, ADP was diagnosed during evaluation of the patient for recurrent pain abdomen and generalized weakness. Jain A, Singh M, Dey S, Kaura A, Diwakar G. A Rare Case of Complete Agenesis of Dorsal Pancreas. Euroasian J Hepato-Gastroenterol 2017;7(2):183-184.

摘要

背侧胰腺发育不全(ADP)是一种极为罕见的先天性异常,由胰腺发育缺陷引起。大多数ADP患者无症状;若有症状,则表现为上腹部疼痛。约一半的患者会因内分泌结构缺失导致胰岛细胞数量减少而患上糖尿病(DM)。由于极为罕见,在处理这些病例时通常不会考虑到,直到进行影像学检查才会被怀疑。在我们的病例研究中,ADP是在对一名反复腹痛和全身无力的患者进行评估时被诊断出来的。Jain A、Singh M、Dey S、Kaura A、Diwakar G。背侧胰腺完全发育不全的罕见病例。《欧亚肝脏胃肠病学杂志》2017年;7(2):183 - 184。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a0c/5670267/7ab5eebcc719/ejohg-07-183-g001.jpg

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