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Solid pseudopapillary neoplasm collides with a well-differentiated pancreatic endocrine neoplasm in an adult man: case report and review of histogenesis.

一例成年男性胰腺实性假乳头状瘤与高分化神经内分泌肿瘤碰撞性肿瘤--病例报告及组织发生回顾

Yan SX,Adair CF,Balani J,Mansour JC,Gokaslan ST

Abstract

Solid pseudopapillary neoplasm (SPN) of the pancreas is a rare, clinicopathologically distinct neoplasm with a tendency to affect young women. The histogenesis of SPN is not well defined. Pancreatic endocrine neoplasms (PENs) are also uncommon tumors of the pancreas.
Our comprehensive review of the literature did not yield any reported cases of collision tumors of the above two neoplasms. We report a case of such a collision tumor in a 45-year-old man.
This tumor was an incidental finding on computed tomography, followed by fine-needle aspiration confirmation of a tumor that was initially diagnosed as an SPN only. A histologic examination of a 2.1-cm mass following distal pancreatectomy revealed a 0.7-cm PEN partly engulfed by an SPN. The tumors showed different morphologic and immunohistochemical features, confirming the presence of a collision tumor.
A comparative analysis of immunoprofiles of these tumors yielded interesting findings, enabling us to postulate that SPNs may originate from a multipotential primordial cell that may follow different differentiation pathways, such as endocrine, epithelial, and acinar. The ultrastructures and immunophenotypic characteristics appear to support this hypothesis.

摘要

胰腺实性假乳头状瘤(SPN)为一种少见的肿瘤,具有好发于年轻女性的独特临床特点。SPN的组织发生尚不清楚。胰腺神经内分泌肿瘤(PENs) 也为胰腺少见肿瘤。

我们复习文献未见上述两种肿瘤碰撞的报道。在此,我们报道一例45岁男性患此碰撞肿瘤的病例。

该肿瘤为CT检查偶然发现,做肿物细针穿刺,病理诊断为SPN。接下来远端胰切除术发现一个2.1cm肿物,其中0.7cm为PEN,部分被SPN包绕。肿物具有完全不同的形态学和免疫组织化学特点,证实了该碰撞性肿瘤的存在。

对这个碰撞性肿瘤的免疫组织化学综合分析有一些有趣的发现,使得我们推测SPN可能起源于多潜能原始细胞,继之以不同的分化方向,如神经内分泌、上皮和腺泡。超微结构和免疫表型特点支持该假设。

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