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背侧胰腺发育不全,急性阑尾炎诊断时的偶然发现;一例病例报告。

Dorsal pancreas agenesis, an incidental finding during acute appendicitis diagnosis; A case report.

作者信息

Kyejo Willbroad, Ismail Allyzain, Panjwani Sajida, Matillya Nancy, Jusabani Ahmed, Datoo Adil, Ally Pilly

机构信息

The Aga Khan University, East Africa Medical College, Tanzania.

The Aga Khan University, East Africa Medical College, Tanzania.

出版信息

Int J Surg Case Rep. 2023 Aug;109:108567. doi: 10.1016/j.ijscr.2023.108567. Epub 2023 Jul 28.

Abstract

INTRODUCTION AND IMPORTANCE

Dorsal pancreas agenesis is a rare congenital anomaly characterized by the absence or severe underdevelopment of the dorsal pancreatic bud. We report a case of a man who presented with features of appendicitis only to the incidentally discovery of dorsal pancreas agenesis during the diagnosis of acute appendicitis. We describe our experience on radiological diagnostic formulation and work up.

CASE PRESENTATION

We present the case of a 45-year-old male patient who presented to the emergency department with symptoms and signs suggestive of acute appendicitis. A computed tomography scan and laboratory investigations confirmed the diagnosis of appendicitis. Incidentally, the scan also revealed the absence of dorsal pancreatic tissue, leading to the incidental diagnosis of dorsal pancreas agenesis.

CLINICAL DISCUSSION

Dorsal pancreas agenesis is often asymptomatic and can be incidentally discovered during imaging studies or surgical interventions for unrelated conditions. In our case, the initial presentation of acute appendicitis provided an opportunity for the fortuitous diagnosis of dorsal pancreas agenesis. This emphasizes the importance of comprehensive imaging reporting in patients who undergo imaging for other conditions.

CONCLUSION

This case report highlights the fortuitous discovery of dorsal pancreas agenesis during the diagnostic workup for acute appendicitis. It emphasizes the need for thorough imaging evaluation and reporting along with the importance of considering anatomical variations in patients presenting with abdominal symptoms. Increased awareness among healthcare professionals about such congenital anomalies can lead to their early recognition and appropriate management.

摘要

引言与重要性

背侧胰腺发育不全是一种罕见的先天性异常,其特征为背侧胰腺芽缺如或严重发育不良。我们报告一例男性患者,该患者最初表现为阑尾炎症状,在急性阑尾炎诊断过程中偶然发现背侧胰腺发育不全。我们描述了我们在放射学诊断分析及检查方面的经验。

病例介绍

我们呈现一例45岁男性患者,该患者因提示急性阑尾炎的症状和体征就诊于急诊科。计算机断层扫描及实验室检查确诊为阑尾炎。偶然的是,扫描还显示背侧胰腺组织缺如,从而偶然诊断为背侧胰腺发育不全。

临床讨论

背侧胰腺发育不全通常无症状,可在影像学检查或针对无关病症的手术干预过程中偶然发现。在我们的病例中,急性阑尾炎的最初表现为偶然诊断背侧胰腺发育不全提供了机会。这强调了对因其他病症接受影像学检查的患者进行全面影像学报告的重要性。

结论

本病例报告突出了在急性阑尾炎诊断检查过程中偶然发现背侧胰腺发育不全。它强调了进行全面影像学评估及报告的必要性,以及考虑有腹部症状患者解剖变异的重要性。医护人员对此类先天性异常的认识提高可导致其早期识别及恰当处理。

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