Suppr超能文献

首次急性发作伴多发假性囊肿并发症后遗传性胰腺炎的诊断

Diagnosis of Hereditary Pancreatitis Following the Initial Acute Episode With Multiple Pseudocyst Complications.

作者信息

Fujiwara Michimasa

机构信息

Pediatrics, National Hospital Organization Fukuyama Medical Center, Fukuyama, JPN.

出版信息

Cureus. 2024 Nov 13;16(11):e73653. doi: 10.7759/cureus.73653. eCollection 2024 Nov.

Abstract

Hereditary pancreatitis (HP) is an unusual form of pancreatitis inherited as an autosomal dominant disorder. Patients typically present with recurrent acute pancreatitis-like symptoms that eventually progress to chronic pancreatitis, resulting in pancreatic exocrine insufficiency or diabetes mellitus, and a high risk of developing pancreatic cancer. As such, early diagnosis is crucial. Herein, we present the case of an 11-year-old boy with no significant medical history, but a family history of type 1 diabetes and pancreatic cancer, who presented with intermittent epigastric pain and nausea. Imaging revealed multiple pancreatic pseudocysts, pancreatic stones, and pancreatic duct dilation, resulting in the diagnosis of acute-on-chronic pancreatitis. Genetic testing confirmed the presence of a mutation in the PRSS1 gene, ultimately resulting in the diagnosis of HP. The patient remained symptom-free for five years during follow-up post-treatment. This case highlights the importance of considering HP in young patients presenting with pseudocysts and other signs of chronic pancreatitis even during the initial acute episode.

摘要

遗传性胰腺炎(HP)是一种不常见的胰腺炎形式,作为常染色体显性疾病遗传。患者通常表现出反复发作的类似急性胰腺炎的症状,最终发展为慢性胰腺炎,导致胰腺外分泌功能不全或糖尿病,以及患胰腺癌的高风险。因此,早期诊断至关重要。在此,我们报告一例11岁男孩的病例,他没有明显的病史,但有1型糖尿病和胰腺癌家族史,出现间歇性上腹部疼痛和恶心。影像学检查发现多个胰腺假性囊肿、胰腺结石和胰管扩张,诊断为慢性胰腺炎急性发作。基因检测证实PRSS1基因存在突变,最终确诊为HP。该患者在治疗后的随访期间五年无症状。这个病例强调了即使在最初的急性发作期,对于出现假性囊肿和其他慢性胰腺炎体征的年轻患者考虑HP的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1cb/11645519/894e52d8a46d/cureus-0016-00000073653-i01.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验