Kosmahl M, Peters K, Anlauf M, Sipos B, Pauser U, Lüttges J, Klöppel G
Institut für Allgemeine Pathologie, Universitätsklinikum Schleswig-Holstein--Campus Kiel, Michaelisstrasse 11, 24105 Kiel, Germany.
Pathologe. 2005 Feb;26(1):41-5. doi: 10.1007/s00292-004-0729-y.
Solid pseudopapillary neoplasms (SPN) of the pancreas represent a special tumor entity, both morphologically and biologically. They form large solitary tumors that occur predominantly in young women. Histologically, they show solid, pseudopapillary, and pseudocystic patterns. The tumor cells are monomorphous and typically express vimentin, neuron-specific enolase, nuclear beta-catenin, and the progesterone receptor. Complete resection cures the tumor in about 90% of the cases. However, because recurrences and even metastases may occur in a small number of cases, SPN are classified as low-grade malignant tumors. Predicting malignancy histologically is not yet possible. The most important differential diagnosis to consider is neuroendocrine tumor of the pancreas. The etiology and pathogenesis of SPN are obscure.
胰腺实性假乳头状肿瘤(SPN)在形态学和生物学上均代表一种特殊的肿瘤实体。它们形成主要发生于年轻女性的大型孤立性肿瘤。组织学上,它们呈现实性、假乳头状和假囊性结构。肿瘤细胞形态单一,通常表达波形蛋白、神经元特异性烯醇化酶、核β-连环蛋白和孕激素受体。在约90%的病例中,完整切除可治愈肿瘤。然而,由于少数病例可能发生复发甚至转移,SPN被归类为低级别恶性肿瘤。目前尚无法通过组织学预测恶性程度。需要考虑的最重要鉴别诊断是胰腺神经内分泌肿瘤。SPN的病因和发病机制尚不清楚。