Matran Elena Roxana, Diaconu Andra-Mihaela, Neagu Oana, Ulmeanu Alexandru-Ioan
Department of Paediatrics, "Carol Davila" University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Department of Pediatrics, "Grigore Alexandrescu" Emergency Hospital for Children, 011743 Bucharest, Romania.
Diagnostics (Basel). 2025 May 8;15(10):1193. doi: 10.3390/diagnostics15101193.
: Ectopic pancreatic tissue (EPT), an infrequently documented condition within the pediatric population, is often asymptomatic. When clinical manifestations do occur, their severity is contingent upon the location, size, and involvement of the adjacent mucosa. : This is a case series study, involving six children aged 15 days-13 years diagnosed with EPT from a single institution. Five of the six cases presented with both EPT and ectopic gastric tissue, located at the site of Meckel's diverticulum, while one case presented EPT exclusively, which was localized in the duodenum I. A case of Littre's hernia was identified in a newborn. Two of the six cases experienced gastrointestinal bleeding. Due to limited data on EPT in children, a comprehensive review of the literature was conducted to integrate the findings of the case series. The review synthesized evidence on clinical manifestations, diagnostic approaches, phenotypic classifications, and management strategies. Articles were identified through searches on PubMed and publisher platforms such as Elsevier and Wiley Online Library, using keywords like "ectopic pancreatic tissue", "heterotopic pancreas", and "pediatric ectopic pancreas". : The identification of EPT continues to pose a diagnostic challenge, as the symptoms are nonspecific and can sometimes be life-threatening. Additionally, there are currently no specific paraclinical investigations available for this purpose. Histopathological evaluation remains crucial for establishing the diagnosis, which is often confirmed only after complications have arisen.
异位胰腺组织(EPT)在儿科人群中是一种记录较少的病症,通常无症状。当出现临床表现时,其严重程度取决于位置、大小以及相邻黏膜的受累情况。 这是一项病例系列研究,涉及来自单一机构的6名年龄在15天至13岁之间被诊断为EPT的儿童。6例中有5例同时存在EPT和异位胃组织,位于梅克尔憩室部位,而1例仅表现为EPT,局限于十二指肠I。在一名新生儿中发现了一例里特疝。6例中有2例出现胃肠道出血。由于儿童EPT的数据有限,因此对文献进行了全面回顾以整合该病例系列的研究结果。该回顾综合了关于临床表现、诊断方法、表型分类和管理策略的证据。通过在PubMed以及爱思唯尔和威利在线图书馆等出版商平台上搜索,使用“异位胰腺组织”、“异位胰腺”和“儿科异位胰腺”等关键词来识别文章。 EPT的识别仍然是一个诊断挑战,因为症状不具有特异性,有时可能危及生命。此外,目前尚无用于此目的的特定辅助临床检查。组织病理学评估对于确立诊断仍然至关重要,通常只有在出现并发症后才能确诊。