| Literature DB >> 33732624 |
Shunya Matsumoto1, Yasukazu Nakanishi1, Kenji Tanabe1, Shugo Yajima1, Reiko Watanabe1, Hitoshi Masuda1.
Abstract
Solid pseudopapillary neoplasm is a rare disease that accounts for approximately 2% of pancreatic neoplasms, and the treatment is complete resection of the tumor. We experienced a case preoperatively diagnosed as a left renal tumor with pancreatic invasion and histologically diagnosed with solid pseudopapillary neoplasm of the pancreas. The purpose of this case report is to illustrate the importance of differentiating solid pseudopapillary neoplasm in patients who present a left renal tumor with pancreatic invasion.Entities:
Keywords: CT, computed tomography; MRI, magnetic resonance imaging; Renal tumor; SPN, solid pseudopapillary neoplasm; Solid pseudopapillary neoplasm
Year: 2021 PMID: 33732624 PMCID: PMC7944025 DOI: 10.1016/j.eucr.2021.101630
Source DB: PubMed Journal: Urol Case Rep ISSN: 2214-4420
Fig. 1Contrast-enhanced computed tomography of the tumor. The maximum tumor diameter was 9cm (A)(B)(yellow arrowhead). The tumor seems to be invaded to the pancreas (C)(D)(orange arrowhead). Calcification was observed (green arrowhead). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2Dynamic study of the contrast-enhanced computed tomography of the tumor. The tumor showed progressive uptake of contrast (yellow arrowhead). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3Solid pseudopapillary neoplasm and the left kidney is well margined (A). Preoperative tumor biopsy revealed papillary tumor (B), which was also observed in resected specimen (C). Β-catenin and synaptophysin were positive (D)(E). Abbreviation: HE (Hematoxylin-Eosin stain).