Raddaoui Emad, Al-Sharabi Abdulsalam, Almadi Majid A
Division of Pathology, King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia, .
Saudi J Gastroenterol. 2015 Mar-Apr;21(2):116-8. doi: 10.4103/1319-3767.153841.
Pancreatic heterotopia is a rare congenital disorder occurring at a variety of sites in the gastrointestinal tract. It is rarely symptomatic. Despite advances in diagnostic techniques, it still remains a challenge to the clinician to differentiate it from a neoplasm. Cytologic characteristics of pancreatic heterotopia in general are rarely described in the literature. We report the cytologic characteristics of heterotopic pancreatic tissue at the gastric outlet in a 48-year-old female. The patient underwent surgical excision due to symptoms related to the lesion. Endoscopic ultrasound fine-needle aspiration is increasingly used for the diagnosis of gastrointestinal tumors, which makes the recognition of certain endoscopically unreachable lesions an important step in optimal patient management.
胰腺异位是一种罕见的先天性疾病，可发生于胃肠道的多个部位。它很少有症状。尽管诊断技术不断进步，但对临床医生来说，将其与肿瘤区分开来仍是一项挑战。胰腺异位的细胞学特征在文献中总体上很少被描述。我们报告了一名48岁女性胃出口处异位胰腺组织的细胞学特征。该患者因与病变相关的症状接受了手术切除。内镜超声细针穿刺越来越多地用于胃肠道肿瘤的诊断，这使得识别某些内镜无法到达的病变成为优化患者管理的重要一步。
