# Pancreatic Metastases from Clear Cell Renal Cell Carcinoma: Diagnostic Insights from Endoscopic Ultrasound-Guided Fine-Needle Biopsy

**Authors:** Alexandru Constantinescu, Ion Dina, Maria Nedelcu, Vlad Dumitru Băleanu, Vasile Florescu, Laura Enache, Octavian Andronic, Daniel Voiculescu, Ancuța Năstac

PMC · DOI: 10.3390/medicina62020239 · 2026-01-23

## TL;DR

This paper discusses how endoscopic ultrasound-guided biopsy helps diagnose pancreatic metastases from kidney cancer, which can be mistaken for primary pancreatic tumors.

## Contribution

The study highlights the diagnostic value of EUS-FNB in distinguishing metastatic ccRCC from primary pancreatic tumors.

## Key findings

- Pancreatic metastases from ccRCC are rare but can mimic primary tumors on imaging.
- EUS-FNB provides accurate tissue diagnosis when imaging is inconclusive.
- Patients with pancreatic ccRCC metastases may have a better prognosis than those with other metastatic sites.

## Abstract

Clear cell renal cell carcinoma (ccRCC) is the most common type of kidney cancer, accounting for approximately 75–80% of all renal carcinomas, and is often diagnosed incidentally on abdominal imaging, such as abdominal ultrasound or CT scan. Among other types of renal cancer, ccRCC is recognized to be highly aggressive due to its metastatic potential, which leads to a poor prognosis and an increased mortality rate. The most common sites of ccRCC metastasis are the lung, lymph nodes, bone, liver, and adrenal glands. Clear cell RCC is the most frequent primary tumor associated with secondary pancreatic involvement, while overall, pancreatic metastases represent only 2–5% of all malignant pancreatic lesions. These metastases often occur many years after nephrectomy and may present as solitary or oligometastatic disease, frequently displaying a paradoxically favorable prognosis compared with other metastatic sites. The present narrative review we conducted emerged from presentations of ccRCC with pancreatic distant metastases, potentially labeled as primary pancreatic tumors on imaging studies, mimicking pancreatic neuroendocrine tumors due to the hypervascular nature of ccRCC. Four patients were investigated in our clinic for suspicious pancreatic lesions identified on CT imaging, involving both the head and body of the pancreas. The definitive diagnosis was established by performing endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) or fine-needle biopsy (FNB) and histopathological analysis of the collected tissue samples. Endoscopic ultrasound-guided fine-needle biopsy (EUS-FNB) has emerged as a pivotal tool for obtaining tissue diagnosis, particularly when cross-sectional imaging is inconclusive. Through a synthesis of clinical data and literature, this article underscores the essential diagnostic role of EUS-guided tissue acquisition and its impact on therapeutic decision-making.

## Linked entities

- **Diseases:** clear cell renal cell carcinoma (MONDO:0005005), ccRCC (MONDO:0007763)

## Full-text entities

- **Genes:** KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, PTPRC (protein tyrosine phosphatase receptor type C) [NCBI Gene 5788] {aka B220, CD45, CD45R, GP180, IMD105, L-CA}, KRT7 (keratin 7) [NCBI Gene 3855] {aka CK7, K2C7, K7, SCL}, VIM (vimentin) [NCBI Gene 7431], CD163 (CD163 molecule) [NCBI Gene 9332] {aka M130, MM130, SCARI1}, FOXP3 (forkhead box P3) [NCBI Gene 50943] {aka AIID, DIETER, IPEX, JM2, PIDX, XPID}, CA9 (carbonic anhydrase 9) [NCBI Gene 768] {aka CAIX, MN}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, PAX8 (paired box 8) [NCBI Gene 7849] {aka PAX-8}, MME (membrane metalloendopeptidase) [NCBI Gene 4311] {aka CALLA, CD10, CMT2T, NEP, SCA43, SFE}, MUC16 (mucin 16, cell surface associated) [NCBI Gene 94025] {aka CA125}, VHL (von Hippel-Lindau tumor suppressor) [NCBI Gene 7428] {aka HRCA1, RCA1, VHL1, pVHL}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, SYP (synaptophysin) [NCBI Gene 6855] {aka MRX96, MRXSYP, XLID96}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}
- **Diseases:** inflammatory (MESH:D007249), injury to (MESH:D014947), hematoma (MESH:D006406), pancreas tumor (MESH:D010190), Tumor (MESH:D009369), abdominal pain (MESH:D015746), pancreatic involvement (MESH:D010195), jaundice (MESH:D007565), kidney cancer (MESH:D007680), neuroendocrine and primary pancreatic tumors (MESH:D018358), Lynch syndrome (MESH:D003123), hypoxia (MESH:D000860), Colonic Adenocarcinoma (MESH:D003110), Pancreatic Metastases (MESH:D009362), peritoneal irritation (MESH:D010538), von Hippel-Lindau (MESH:D006623), renal involvement (MESH:C565423), protrusive duodenal lesion (MESH:D004378), lymphoma (MESH:D008223), urogenital, breast, or lung tumors (MESH:D001943), ovarian and colorectal cancers (MESH:D010051), mRCC (MESH:C538445), Pancreatic lesion (MESH:D010182), ccRCC (MESH:D002292), gastrointestinal bleeding (MESH:D006471), colonic involvement (MESH:D003108)
- **Chemicals:** Adrenalin (MESH:D004837), Hematoxylin (MESH:D006416)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942382/full.md

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Source: https://tomesphere.com/paper/PMC12942382