Congenital pancreas malformations: a clinical case report

Ana Bento, Hamilton Baptista, Fernando Oliveira
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引用次数: 5

Abstract

Objective

This study aimed to review the congenital malformation known as agenesis of the dorsal pancreas (ADP) and other pancreatic birth defects, based on a rare and exemplary clinical case of pancreatic malformations. The intent was to review the latest information published in the national and international literature on pancreatic birth defects, and to investigate the diversity of clinical presentations of ADP and other congenital pancreas abnormalities. The purpose was to identify which situations have therapeutic indication, the most appropriate time to institute treatment, and the currently available medical or surgical treatment of pancreatic congenital malformations.

Results

ADP is a very rare malformation that occurs during organogenesis. In the last decades, a large volume of embryological and genetic information has been obtained, helping to understand the causes of pancreatic malformations, which must be studied and understood as a whole.

Conclusion

Pancreatic malformations are infrequently studied causes of acute and chronic pancreatitis in adults. The possibility of pancreatic malformations should always be considered in patients with acute or chronic pancreatitis with no evident cause.

先天性胰腺畸形1例临床报告
目的本研究旨在回顾先天性胰腺背侧发育不全(ADP)和其他胰腺出生缺陷,基于一个罕见和典型的胰腺畸形临床病例。目的是回顾发表在国内和国际上关于胰腺出生缺陷的最新信息,并研究ADP和其他先天性胰腺异常的临床表现的多样性。目的是确定哪些情况有治疗指征,最合适的时间进行治疗,以及目前可用的药物或手术治疗胰腺先天性畸形。结果adp是一种在器官发生过程中极为罕见的畸形。在过去的几十年里,已经获得了大量的胚胎学和遗传学信息,有助于了解胰腺畸形的原因,这必须作为一个整体来研究和理解。结论胰腺畸形是成人急慢性胰腺炎的罕见病因。没有明显病因的急性或慢性胰腺炎患者应始终考虑胰腺畸形的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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