首页> 美国卫生研究院文献>International Journal of Clinical and Experimental Pathology >Solid pseudopapillary neoplasm (SPN) of the pancreas presenting with ascites misdiagnosed as pancreatic tuberculosis: a case report and literature review
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Solid pseudopapillary neoplasm (SPN) of the pancreas presenting with ascites misdiagnosed as pancreatic tuberculosis: a case report and literature review

机译:胰腺实性假乳头状瘤(SPN)伴有被误诊为胰腺结核的腹水:一例病例并文献复习

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摘要

Introduction: Solid pseudopapillary neoplasm (SPN) is a rare pancreatic tumor that mainly affects young women. It is a low-grade malignant neoplasm, with an excellent prognosis after surgical treatment. We report herein a case of SPN presenting with ascites that was misdiagnosed as pancreatic tuberculosis (TB). Case report: A 16-year-old female initially presented with a large volume of ascites. Contrast-enhanced ultrasound and computed tomography found a heterogeneous lesion in the pancreatic body, which had slight contrast enhancement on the arterial phase. Analysis of ascites showed it was exudative. Endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) of the mass only revealed a few blood clots. The diagnosis was highly suggestive of a pancreatic TB. However, after 6 months of anti-TB therapy, the pancreatic lesion remained essentially unchanged. Subsequently, magnetic resonance imaging indicated a mixed solid and cystic lesion with a well-defined margin in the pancreatic body. Further EUS-FNA showed monomorphic neoplastic cells with papillary architecture and immunohistochemical analysis revealed that the tumor cells were positive for β-catenin, CD10, vimentin, cytokeratin, and synaptophysin. These findings were consistent with SPN. After distal pancreatectomy with splenectomy, postoperative pathology and immunohistochemical staining confirmed the diagnosis of SPN. Conclusion: Clinicians should consider the possibility of SPN for pancreatic heterogeneous masses. Multiple diagnostic imaging modalities and EUS-FNA may contribute to the preoperative diagnosis of this disease.
机译:简介:实体假乳头状肿瘤(SPN)是一种罕见的胰腺肿瘤,主要影响年轻女性。它是低度恶性肿瘤,手术治疗后预后良好。我们在此报告一例SPN伴有被误诊为胰腺结核(TB)的腹水。病例报告:最初有一名16岁女性出现大量腹水。对比增强超声和计算机断层扫描发现胰体中存在异质性病变,在动脉期具有轻微的对比增强。腹水分析表明它是渗出的。内镜超声引导下的细针穿刺抽吸(EUS-FNA)仅显示出一些血块。该诊断强烈提示胰腺结核。但是,抗结核治疗6个月后,胰腺病变基本保持不变。随后,磁共振成像显示胰体中边缘清晰明确的实性和囊性混合病变。进一步的EUS-FNA显示具有乳头状结构的单形肿瘤细胞,免疫组织化学分析显示肿瘤细胞对β-catenin,CD10,波形蛋白,细胞角蛋白和突触素呈阳性。这些发现与SPN一致。远端胰腺切除术并脾切除术后,术后病理和免疫组化染色证实了SPN的诊断。结论:临床医生应考虑SPN治疗胰腺异质性肿块的可能性。多种诊断成像方式和EUS-FNA可能有助于对该疾病的术前诊断。

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