Garg Bhavna, Sood Neena, Kaur Harpreet, Mittal Divya
J Assoc Physicians India. 2014 Jan;62(1):61-4.
A solid pseudopapillary tumour of the pancreas (SPT) is a rare neoplasm accounting for less than 2% of exocrine pancreatic neoplasms. SPT occurs in adolescent young females and is mostly benign. It is a low-grade malignant tumour that may evolve years before symptoms start and has a favourable prognosis. In this report we present five cases (four females, one male, aged 16, 45, 23, 17 and 55 years, respectively) of SPT localised in the pancreas, and discuss the clinical, imaging and histologic findings with a review of the literature. We retrospectively reviewed these five patients with SPT who underwent surgical resection in our hospital with a definitive histologic diagnosis of SPT.
胰腺实性假乳头状瘤（SPT）是一种罕见的肿瘤，占胰腺外分泌肿瘤的比例不到2%。SPT好发于青春期年轻女性，大多为良性。它是一种低度恶性肿瘤，可能在症状出现前数年就已发生，预后良好。在本报告中，我们呈现了5例胰腺局限性SPT病例（4例女性，1例男性，年龄分别为16岁、45岁、23岁、17岁和55岁），并结合文献复习讨论了其临床、影像学和组织学表现。我们回顾性分析了我院5例接受手术切除且经组织学确诊为SPT的患者。
