Xiaoxiao Bao
Chunyan Chen- Department of Pathology, Affiliated Dongyang Hospital of Wenzhou Medical University, Dongyang, Zhejiang, China
Introduction: Gastrointestinal stromal tumors (GISTs), mesenchymal neoplasms of the gastrointestinal tract, are prone to recurrence and metastasis. Despite improvements in prognosis with targeted treatments, such as imatinib, some patients develop metastatic GIST. Renal involvement in GIST is uncommon, and data on the diagnosis and treatment of GIST with renal metastasis remain limited. In this report, we describe the diagnostic and therapeutic regimen used for a patient with renal metastasis from GIST, providing an important reference for clinicians.
Case presentation: A 52-year-old man underwent resection of a gastric GIST 5 years previously and had received adjuvant imatinib therapy for 2 years. A radical nephrectomy was performed, and histopathological analysis confirmed metastatic GIST. Although the patient resumed imatinib therapy post-surgery, follow-up imaging 22 months later revealed multiple metastases in the retroperitoneum and abdominal cavity.
Conclusion: Renal metastasis from GIST is highly aggressive. Although surgical resection offers considerable palliation and may prolong survival, survival is generally dependent on sustained multimodal therapy and follow-up. Early detection and management of recurrent or metastatic lesions are imperative to optimize long-term outcomes.
1 Introduction
Gastrointestinal stromal tumors (GISTs) are mesenchymal tumors originating from the gastrointestinal tract (1, 2). The pathogenesis of GIST is complex, primarily involving mutations in the KIT or PDGFRA genes (3, 4). Despite a recent rise in the incidence of GIST, clinical diagnosis and management remain challenging. Whereas the liver is a common site of GIST metastasis, renal involvement tends to be rare. Kidney-metastatic GIST may mimic primary renal carcinomas, with small tumors typically being asymptomatic, whereas large tumors can cause flank or abdominal pain, hematuria, and abdominal masses.
In this report, we describe a retrospective analysis of the clinical and pathological features, treatment, and prognosis of a patient with kidney-metastatic GIST treated at Dongyang People’s Hospital, aimed at providing a reference for clinicians managing similar cases.
2 Case description
On October 21, 2020, a 52-year-old man presented with intermittent-to-severe pain in the left abdomen and flank, which had persisted for 6 months and had worsened over the preceding 12 days. The pain, although non-radiating, was severe. The patient denied having any associated symptoms, such as nausea, vomiting, hematemesis, melena, chest tightness, dyspnea, altered bowel or bladder habits, dysuria, hematuria, or constitutional weakness.
On physical examination, the abdomen was soft and non-distended. The left upper abdomen was full, and a firm mass measuring 15 × 12 cm, with poor mobility and adhesion to surrounding tissues, was palpated. Although the overlying skin showed no evidence of redness or swelling, mild tenderness without rebound pain was detected, and percussion over both renal angles elicited no discomfort.
Approximately 5 years prior to presentation (July 15, 2015), the patient had undergone laparotomy with a partial gastrectomy and splenectomy under general anesthesia for resection of a gastric tumor. The tumor, measuring 7 × 6 × 5 cm on the greater curvature near the cardia, had penetrated the serosa and extended to the splenic hilum and pancreatic tail, involving the splenic vessels. Several enlarged lymph nodes were palpable around the area. Postoperative pathology revealed an intermediate-risk GIST (Figure 1). The tumor, measuring 5.5 × 5.0 cm, was positive for smooth muscle actin, CD117, and CD34; and negative for S-100, with a Ki-67 proliferation index of 15%. The resection margins were negative, and he completed 2 years of oral imatinib (400 mg once daily) without evidence of recurrence during follow-up. The timeline, including key events, is summarized in Table 1.
Figure 1. Histopathological and immunohistochemical features of a gastric gastrointestinal stromal tumor (GIST). (A) The tumor cells are arranged in bundles with myxoid stromal change. [hematoxylin and eosin (H&E), ×100]. (B) The tumor cells are spindle-shaped or short spindle-shaped (H&E, ×400). (C) The tumor cells strongly express CD117 (immunohistochemistry, ×200). (D) The tumor cells strongly express DOG-1 (immunohistochemistry, ×200).
Table 1. Chronology of the key diagnostic and therapeutic events from the initial gastrointestinal stromal tumor (GIST) resection (2015) to renal metastasis management and subsequent disease progression 22 months after nephrectomy.
3 Diagnostic assessment
On October 24, 2020, retroperitoneal computed tomography (CT) revealed a left retroperitoneal mass measuring 16.3 × 12.0 cm with relatively well-defined margins abutting the left kidney. Heterogeneous low-density areas were present, and contrast enhancement was uneven. However, no enlarged regional lymph nodes were observed. Retroperitoneal CT revealed a large left-sided retroperitoneal mass, suspected to be of renal origin (renal carcinoma), and magnetic resonance imaging (MRI) with contrast was recommended (Figure 2).
Figure 2. Contrast-enhanced computed tomography (CT) findings for a kidney-metastatic gastrointestinal stromal tumor (GIST). (A) Plains showing a large left retroperitoneal mass of near-equal attenuation containing patchy low-density foci. (B) Arterial phase image revealing mild heterogeneous enhancement with multiple tortuous arteries and intralesional arteries, whereas the low-density foci remain unenhanced. (C) Venous-phase image showing continued enhancement of the solid components, whereas the low-density areas seen on the plain scan remain unenhanced. (D) Coronal arterial phase reconstruction showing the arterial supply from branches of the left renal artery. The mass obscures the boundary with the upper pole of the left kidney, which is compressed and displaced inferiorly.
On October 27, 2020, contrast-enhanced MRI confirmed a left renal mass measuring 15.7 × 13.6 cm with a slightly lower signal on T1-weighted images, a heterogeneously high signal on T2-weighted images, and fat-suppressed sequences showing restricted diffusion on diffusion-weighted images, with marked heterogeneous enhancement during the arterial phase and reduced enhancement in the parenchymal phase. Collectively, these findings provided strong evidence of malignancy.
4 Therapeutic intervention and pathology
On November 2, 2020, the patient underwent radical left nephrectomy, with a tumor measuring 18 × 11 × 10 cm being resected. Postoperative pathology revealed histology and immunohistochemistry consistent with a high-risk GIST (Figure 3). Subsequently, immunohistochemical analyses indicated positivity for CD117,CD34, discovered on GIST-1 (DOG-1) and vimentin; and negativity for smooth muscle actin, desmin, actin, S-100, and cytokeratin (CK). A Ki-67 proliferation index of approximately 70% was identified. The perinephric fat, ureteral margin, and vascular invasion were negative of tumor. In addition, a KIT exon 11 mutation was identified. Imatinib therapy (400 mg once daily) was resumed on postoperative day 5.
Figure 3. Histopathological and immunohistochemical features of a kidney-metastatic gastrointestinal stromal tumor (GIST). (A) Composite section showing normal renal parenchyma above and epithelioid-cell GIST below (H&E, ×100). (B) Magnified view showing epithelioid tumor cells with round to oval nuclei, clear to eosinophilic cytoplasm, frequent mitoses, and extensive necrosis (H&E, ×400). (C) The tumor cells strongly express CD117 (immunohistochemistry, ×200). (D) The tumor cells strongly express DOG-1 (immunohistochemistry, ×200).
5 Follow-up and outcomes
Although the patient continued to receive imatinib over the course of the 22-month follow-up, subsequent imaging revealed multiple metastases in the retroperitoneum and abdominal cavity, indicating disease progression.
6 Discussion
Metastatic renal tumors originate from extrarenal malignancies. Although the kidneys are not a common target, most solid cancers can undergo renal metastasis (5). GIST is derived from the interstitial cells of Cajal, which serve as gastrointestinal pacemaker cells. These tumors most commonly metastasize to the liver, followed by the lungs and bones, whereas renal metastasis is rare (6). To the best of our knowledge, solitary renal metastasis from a gastric GIST has not previously been reported in the English-language literature. Clinical manifestations generally resemble those associated with primary renal carcinomas, with patients often initially being asymptomatic. As the tumor progresses, patients may experience persistent or intermittent flank or abdominal pain, visible hematuria, or a palpable lump (7). However, although renal lesions are rare at the initial GIST diagnosis, they are typically detected during the advanced stages characterized by metastatic spread.
Imaging plays a particularly important role in diagnosing kidney-metastatic GIST. However, although CT and MRI can accurately determine the location, size, and morphology of a lesion, the wide spectrum of primary renal neoplasms tends to be characterized by a broad radiological overlap, thereby rendering definitive identification difficult. Consequently, pathological examination remains the diagnostic gold standard because it can distinguish the three histological subtypes (spindle cells, epithelioid cells, and mixed types), while also revealing characteristic immunoreactivity to CD117 and DOG-1. Histological analyses also contribute to excluding the probability of similar tumors, such as primary renal carcinomas, which express CK and paired box gene 8 rather than CD117 or DOG-1, and angiomyolipomas, which generally comprise fat tissue, smooth muscle, and thick-walled blood vessels and tend to be positive for human melanoma black 45 and Melan-A but negative for CD117 and DOG-1.
Under conditions in which the extent of GIST metastasis is restricted, surgical resection remains the standard intervention, and complete surgical removal of lesions can significantly improve patient prognosis (8). However, multifocal metastatic GIST typically requires multi-organ resection, thereby necessitating a thorough abdominal examination. Nevertheless, if the metastatic proliferation is too extensive for curative surgery, resection should be avoided, as a prolonged recovery can delay systemic therapy with imatinib, which is currently the mainstay treatment for primary and metastatic GIST. Consequently, surgical complexity and overall tumor burden are considered key determinants in establishing the resectability of metastatic GIST (9). Although imatinib offers an appreciable advantage for patients with metastatic GIST who are either inoperable or at high surgical risk, secondary KIT mutations frequently lead to resistance to imatinib within 18–24 months (10). Among promising alternative approaches, ongoing molecular research has prompted trials examining the efficacy of inhibitors of the mammalian target-of-rapamycin and immune checkpoint molecules (11).
In the case reported herein, the patient underwent partial gastrectomy for a moderate-risk gastric GIST in 2015 and maintained 2-year disease-free survival on adjuvant imatinib. Five years later, a large renal mass was detected, with radical nephrectomy confirming metastatic GIST, and imatinib therapy was initiated. However, despite an initial response, multiple retroperitoneal and intraperitoneal metastases emerged 22 months after nephrectomy, indicating the development of imatinib resistance and a poor prognosis. When kidney metastasis is confirmed, surgery can contribute to a significant improvement in outcomes, with imaging serving as an indispensable diagnostic aid, nevertheless, histopathology remains the diagnostic gold standard.
In conclusion, renal metastases from GISTs are exceedingly uncommon, and there is currently no established standard of care. Preoperative imaging frequently misdiagnosis these lesions as primary renal cell carcinomas; therefore, accurate diagnosis relies on histopathology, immunohistochemistry, and molecular profiling. Although complete surgical resection of large renal masses can provide rapid relief from symptoms, adjuvant imatinib remains mandatory. For patients who exhibit resistance, multidisciplinary teams of practitioners should design personalized, multimodal treatment plans to extend survival and optimize the quality of life.
Data availability statement
The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author.
Ethics statement
Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.
Author contributions
XB: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Supervision, Visualization, Writing – original draft, Writing – review & editing. CC: Conceptualization, Data curation, Formal analysis, Methodology, Project administration, Writing – original draft, Writing – review & editing. BH: Conceptualization, Data curation, Formal analysis, Project administration, Software, Visualization, Writing – original draft, Writing – review & editing.
Funding
The author(s) declare that no financial support was received for the research, and/or publication of this article.
Acknowledgments
We would like to thank Editage (www.editage.cn) for English language editing.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Abbreviations
GIST, Gastrointestinal stromal tumor; DOG-1, Discovered on GIST-1; CK, Cytokeratin; CT, Computed tomography; MRI, Magnetic resonance imaging.
References
1. Akahoshi K, Oya M, Koga T, and Shiratsuchi Y. Current clinical management of gastrointestinal stromal tumor. World J Gastroenterol. (2018) 24:2806–17. doi: 10.3748/wjg.v24.i26.2806
2. Keung EZ and Raut CP. Management of gastrointestinal stromal tumors. Surg Clin North Am. (2017) 97:437–52. doi: 10.1016/j.suc.2016.12.001
3. Schaefer IM, Mariño-Enríquez A, and Fletcher JA. What is new in gastrointestinal stromal tumor? Adv Anat Pathol. (2017) 24:259–67. doi: 10.1097/PAP.0000000000000158
4. Venkataraman V, George S, and Cote GM. Molecular advances in the treatment of advanced gastrointestinal stromal tumor. Oncologist. (2023) 28:671–81. doi: 10.1093/oncolo/oyad167
5. Wu AJ, Mehra R, Hafez K, Wolf JS, and Kunju LP. Metastases to the kidney: a clinicopathological study of 43 cases with an emphasis on deceptive features. Histopathology. (2015) 66:587–97. doi: 10.1111/his.12524
6. Schrage Y, Hartgrink H, Smith M, Fiore M, Rutkowski P, Tzanis D, et al. Surgical management of metastatic gastrointestinal stromal tumour. Eur J Surg Oncol. (2018) 44:1295–300. doi: 10.1016/j.ejso.2018.06.003
7. Saeed F and Osunkoya AO. Secondary tumors of the kidney: a comprehensive clinicopathologic analysis. Adv Anat Pathol. (2022) 29:241–51. doi: 10.1097/PAP.0000000000000338
8. Yonkus JA, Alva-Ruiz R, and Grotz TE. Surgical management of metastatic gastrointestinal stromal tumors. Curr Treat Options Oncol. (2021) 22:37. doi: 10.1007/s11864-021-00837-0
9. Fairweather M, Cavnar MJ, Li GZ, Bertagnolli MM, DeMatteo RP, and Raut CP. Prediction of morbidity following cytoreductive surgery for metastatic gastrointestinal stromal tumour in patients on tyrosine kinase inhibitor therapy. Br J Surg. (2018) 105:743–50. doi: 10.1002/bjs.10774
10. Ang C and Maki RG. Contemporary management of metastatic gastrointestinal stromal tumors: systemic and locoregional approaches. Oncol Ther. (2016) 4:1–16. doi: 10.1007/s40487-015-0014-7
Keywords: gastrointestinal stromal tumor, distant metastasis, kidney, treatment, prognosis
Citation: Bao X, Chen C and Huang B (2025) Case Report: Renal metastasis of a gastric gastrointestinal stromal tumor mimicking a primary renal carcinoma. Front. Oncol. 15:1669412. doi: 10.3389/fonc.2025.1669412
Received: 19 July 2025; Accepted: 12 September 2025;
Published: 01 October 2025.
Edited by:
Zhen Liu, Zhejiang University, ChinaReviewed by:
Linfeng Zheng, Zhejiang Cancer Hospital, ChinaShufei Wei, Jiujiang University Affiliated Hospital, China
Copyright © 2025 Bao, Chen and Huang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Bifei Huang, aGJmeDcxMTAyM0AxNjMuY29t