Tesaříková J, Loveček M, Neoral Č, Vomáčková K, Bébarová L, Skalický P
Rozhl Chir. 2017 Spring;96(4):163-167.
Solid pseudopapillary neoplasm (SPN) is a very rare neoplasm that occurs in girls and young women in 90% of cases; the range is 779 years of age, and the median is 28 years of age. This tumour was first described by Virginia Frantz in 1959 as a papillary cystic tumour of the pancreas.
The aim of this retrospective study was to analyse the incidence of SPN in all patients with a pancreatic tumour operated at the 1st Dept. of Surgery, University Hospital Olomouc between years 2006 and 2015. Clinical symptoms, imaging methods used, tumour marker positivity, histological findings, postoperative complications and disease-free interval were all evaluated.
Of the 454 patients operated on between 20062015, the diagnosis of SPN was made in five female patients. The following imaging methods were used in the preoperative diagnostic process: CT, MRI, PET/CT and endosonography. In four patients the tumour was localised in the tail of the pancreas; these women underwent left-sided pancreatectomy. In one patient, the tumour was located in the pancreatic head and a pylorus-preserving pancreaticoduodenectomy was performed. Complications were seen only in one patient who underwent revision on the first postoperative day for bleeding from the pancreatic cut surface. Pancreatic fistula was not observed in any of the patients. The procedures were considered as sufficient from the oncological viewpoint due to the radical resection procedure and negative resection margin, and therefore no adjuvant oncological treatment was indicated in any of the patients. During the follow-up period, recurrence was not observed in any one of the patients.
Solid pseudopapillary neoplasm of the pancreas is a rare disorder with a low malignant potential occurring primarily in young women. Generally, SPN has a good prognosis; however, advanced stages of the disease with distant metastases may be encountered in rare cases. The only curative treatment is radical surgical resection.Key words: solid pseudopapillary neoplasm Frantzs tumour pancreas.
实性假乳头状肿瘤(SPN)是一种非常罕见的肿瘤,90%的病例发生于女孩和年轻女性;年龄范围为7 - 79岁,中位年龄为28岁。该肿瘤于1959年由弗吉尼亚·弗兰茨首次描述为胰腺乳头状囊性肿瘤。
本回顾性研究的目的是分析2006年至2015年在奥洛穆茨大学医院第一外科接受手术的所有胰腺肿瘤患者中SPN的发病率。对临床症状、使用的影像学方法、肿瘤标志物阳性情况、组织学发现、术后并发症和无病间期进行了评估。
在2006 - 2015年间接受手术的454例患者中,有5例女性患者被诊断为SPN。术前诊断过程中使用了以下影像学方法:CT、MRI、PET/CT和内镜超声检查。4例患者的肿瘤位于胰尾;这些女性接受了左侧胰腺切除术。1例患者的肿瘤位于胰头,进行了保留幽门的胰十二指肠切除术。仅1例患者出现并发症,该患者在术后第一天因胰切面出血接受了再次手术。所有患者均未观察到胰瘘。由于根治性切除手术和阴性切缘,从肿瘤学角度来看,手术被认为是充分的,因此所有患者均未进行辅助肿瘤治疗。在随访期间,所有患者均未观察到复发。
胰腺实性假乳头状肿瘤是一种罕见疾病,恶性潜能低,主要发生于年轻女性。一般来说,SPN预后良好;然而,罕见情况下可能会遇到伴有远处转移的疾病晚期。唯一的治愈性治疗方法是根治性手术切除。关键词:实性假乳头状肿瘤;弗兰茨氏肿瘤;胰腺