Wu Hao, Huang Yan-Fen, Liu Xiang-Hong, Xu Mei-Hua
Department of Gastroenterology, Xiangya Hospital of Central South University, Changsha 410008, Hunan Province, China.
World J Gastrointest Oncol. 2017 Dec 15;9(12):497-501. doi: 10.4251/wjgo.v9.i12.497.
Solid pseudopapillary neoplasm (SPN), also known as Gruber-Frantz tumor, is a rare form of neoplasm that almost exclusively occurs in the pancreas and in young females. While the potential of malignancy is low for SPN, these tumors can mimic other diseases and require a meticulous investigation and a standard treatment by total surgical resection. We present an unusual case of SPN arising in the mesentery of a 40-year-old man with subsequent multiple metastases. Histopathological examination showed similar properties of the mesenteric neoplasm to those of SPN in pancreas. Although the mass was surgically removed, the patient died of recurrent disease 4 years after the initial presentation. We speculate that SPN originates from pancreatic progenitor cells. Further histopathological analyses are required for the prediction of SPN recurrence after resection.
实性假乳头状肿瘤(SPN),也称为格鲁伯-弗兰茨肿瘤,是一种罕见的肿瘤形式,几乎只发生于胰腺和年轻女性。虽然SPN的恶性潜能较低,但这些肿瘤可模仿其他疾病,需要进行细致检查并通过完整手术切除进行标准治疗。我们报告一例罕见的SPN病例,发生于一名40岁男性的肠系膜,随后出现多处转移。组织病理学检查显示肠系膜肿瘤与胰腺SPN具有相似特征。尽管肿块已通过手术切除,但患者在初次就诊4年后因疾病复发死亡。我们推测SPN起源于胰腺祖细胞。需要进一步的组织病理学分析来预测SPN切除术后的复发情况。