Case Reports in Medicine

Case Reports in Medicine / 2019 / Article

Case Report | Open Access

Volume 2019 |Article ID 7480479 |

Davi dos Santos Romao, Natally Horvat, Marianne Castro Gonçalves, Emerson Shigueaki Abe, Rodrigo Blanco Dumarco, Publio Cesar Cavalcante Viana, Marcel Cerqueira Cesar Machado, "Isolated Splenic Metastases from Renal Cell Carcinoma 11 Years after Surgery", Case Reports in Medicine, vol. 2019, Article ID 7480479, 6 pages, 2019.

Isolated Splenic Metastases from Renal Cell Carcinoma 11 Years after Surgery

Academic Editor: Lothar Bergmann
Received14 Apr 2019
Revised30 Jun 2019
Accepted01 Sep 2019
Published24 Sep 2019


Splenic metastases are rare and usually occur in cases of disseminated disease. We report a case of a patient who had isolated splenic metastases with a previous history of left nephrectomy due to a renal cell carcinoma 11 years before. The aim of this report is to describe the case and review the literature of isolated splenic metastases due to renal carcinoma. This case emphasizes the importance of considering splenic metastatic disease even after many years of diagnosis of renal cell carcinoma.

1. Introduction

Splenic tumors, primary or metastatic, are rare and most commonly caused by haematological malignancies. The most frequent primary tumors that metastasize to the spleen are malignant melanoma, breast cancer, and lung and ovarian carcinoma [1], and it is usually a part of a disseminated metastatic disease. Metastatic disease is common in renal- cell carcinoma (RCC), and it is frequent to the lungs, bone, liver, adrenal glands, stomach, pancreas, brain, and contralateral kidney [2]. However, isolated splenic metastases from RCC are extremely rare. To the best of our knowledge, there are less than 20 cases of isolated splenic metastases from RCC reported in the literature [1, 316].

The aim of this report is to describe a case of an adult patient with a previous history of left nephrectomy due to an RCC who had isolated splenic metastases 11 years after the primary renal tumor.

2. Case Report

A 48-year-old man complained of intermittent pain in the left flank that started 4 months ago, and it was associated with nausea. Physical examination was normal, except for mild discomfort in the upper abdomen. Laboratory studies were also within normal limits.

He had a previous history of RCC (Figure 1) when he underwent left nephrectomy 11 years before (pT2, pV0, and pN0; Fuhrman grade 1). The RCC infiltrated beyond the renal capsule, but it was contained within the Gerota’s fascia. Pathology showed a subtype of clear cell RCC. He also had a history of B-cell non-Hodgkin lymphoma on the scalp 8 years earlier, which was treated with surgery and radiotherapy.

Abdominal computed tomography (CT) with intravenous contrast was requested to evaluate his symptoms. CT scan demonstrated two heterogeneous hypovascular splenic masses with necrotic areas, situated in the posteroinferior portion. The lesions extended through the splenic capsule and abutted the left diaphragm (Figure 2). Magnetic resonance imaging (MRI) was requested for further evaluation and demonstrated the splenic masses, with lobulated contours, heterogeneous signal intensity, and central necrotic areas (Figure 3). The splenic masses measured 4.5 cm and 5.8 cm. Additionally, a whole-body positron emission tomography scan (PET/CT) was performed, and it revealed an increase in FDG uptake within the splenic mass (SUV: 9.0), without other suspicious lesions (Figure 4).

The patient underwent splenectomy. On pathological examination, the spleen had two yellowish lesions (Figure 5), measuring up to 6.0 cm. On histopathological analysis, areas of tumoral necrosis, angiolymphatic invasion, and focal involvement of the diaphragm were observed. Immunohistochemistry assay was positive for CK8/18, CD10, PAX8, and vimentin, being consistent with metastases of clear cell RCC (Figures 6 and 7). It is important to note that PAX8 fixation was positive for nuclear staining although weak likely due to poor splenic parenchyma fixation (Figure 7(c)). The patient is in his 3rd month after surgery with complete resolution of his symptoms and in a good general health condition.

3. Discussion

Splenic metastases are rare and usually occur in cases of disseminated disease. Isolated splenic metastases from RCC are extremely rare. This rarity might be explained by several theories related to the anatomical, histological, and immunological characteristics of the spleen. The theories include the following: (a) sharp angle of the splenic artery, which may impair the migration of the tumor emboli to the spleen; (b) physiological rhythmic contractile activity of the spleen, squeezing out the tumor emboli; (c) absence of afferent lymphatics, which could bring tumor cells; and (d) high concentration of lymphoid tissue in the spleen, resulting in antitumor activity [3].

There is an estimation that 18% of patients with RCC have metastasis at diagnosis (synchronous metastasis), and after surgical excision, 20%–30% of patients with localized tumors experience relapse [17]. The majority of recurrences (85%) occur within the first 3 years of follow-up. The most common sites of metastatic disease from RCC are the lungs, bone, lymph node, and liver [18].

Isolated spleen metastases may be underestimated, considering that the patients are often asymptomatic or oligosymptomatic. However, recently, more cases of isolated splenic metastases have been diagnosed due to the widespread use of diagnostic imaging modalities. Splenic metastases originating from RCC may be detected synchronously with the renal tumor in 30% of the cases [9] or soon after its diagnosis. However, they can also arise several years after the treatment of the primary tumor as presented in our case.

Isolated splenic metastases from RCC are extremely rare, and to the best of our knowledge, up to now, there are less than 20 cases reported in the literature [1, 316]. Table 1 summarizes the main studies that reported the cases of splenic metastases from RCC [1, 316].

AuthorAge/sexMetastasizing timePrimary (kidney)SymptomsOutcomeHistology typeImaging findingsMet size

Strum [4]59 y/M22 yRightCSDead (5 mo)NS-RCCNDND
Ishida et al. [5]50 y/M7 yLeftAlive (6 y)NS-RCCUS: one solid-cystic mass with echogenic margin4.0 cm
Nabi et al. [14]50 y/F(synchronous)LeftPAlive (6 mo)NS-RCCCT: one solid-cystic hypoattenuating splenic massND
Kugel et al. [6]72 y/M2 yLeftCSDead (1 y)CC-RCCT: one solid-cystic hypoattenuating splenic mass8.0 cm
McGregor et al. [7]65 y/M(synchronous)LeftCS, PNDP-RCCCT: one hypoattenuating, heterogeneously enhancing, splenic mass8.0 cm
Shuck-Bello et al. [15]74 y/M15 yRightNDCC-RCCT and MRI: one hypoattenuating (CT), hypervascular splenic mass with calcificationsND
Ielpo et al. [9]82 y/M14 yLeftAlive (1 y 3 mo)NS-RCC(i) CT: one solid-cystic hypovascular mass
(ii) PET/CT: no metabolic activity
6.0 cm
Moir et al. [10]70 y/F11 moLeftCSAlive (2 y)CC-RCCT: one solid-cystic hypervascular splenic mass7.0 cm
Nunes et al. [11]60 y/F5 yLeftAlive (6 mo)CC-RC(i) CT and MRI: one small hypervascular splenic nodule
(ii) MRI (6 mo later): heterogeneous hypervascular mass with central necrosis
1.0 cm–4.0 cm
Hardikar [16]29 y/M(synchronous)LeftAlive (2 y)CC-RCCT: one hypoattenuating splenic massND
Zhang et al. [12]67 y/M2 yLeftCSAlive (5 mo)NS-RCC(i) CT w/o contrast: one isoattenuating splenic mass
(ii) PET/CT: one hypermetabolic mass
11.4 cm
Grewal et al. [1]53 y/M2 moLeftNDCC-RCPET/CT: multiple splenic lesions, one hypermetabolicND
Liu et al. [13]75 y/M(synchronous)RightCSAlive (1 y 4 mo)P-RCC(i) CT: one indeterminate hypodensity
(ii) CT (9 mo later): heterogeneous splenic mass
0.6–9.9 cm
Romão, 201948 y/M11 yLeftPAlive (2 mo)CC-RCC(i) CT and MRI: two solid-cystic hypervascular masses
(ii) PET/CT: two hypermetabolic masses
5.8 cm

CS: constitutional symptoms, such as weight loss and fatigue; P: pain; ND: not described; NS-RCC: nonspecified renal cell carcinoma; CC-RC: clear cell renal carcinoma; P-RCC: papillary renal cell carcinoma.

The average age of patients with splenic metastases from RCC was 62 years, ranging from 29 to 75 years, and the majority were men (11/14, 78%). The majority of the renal primary tumors was in the left kidney (10/14, 71%), which led to a hypothesis of direct spread of the tumor cells rather than haematogenous metastasis; however, the Gerota’s fascia was intact in the majority of the tumors [10] similar to our case which suggests that it is an isolated metastasis rather than a case of local recurrence. Patients with splenic metastases from RCC were asymptomatic (6/14, 43%) or had abdominal pain or constitutional symptoms, such as fever, fatigue, weight loss, and anemia. The splenic renal metastases were diagnosed at the same time of the primary tumor in 5/14 (36%) cases (synchronous metastases). Among the metachronous cases, the metastasizing interval between the primary renal tumor and the splenic metastasis varied from 2 months to 22 years. Among the cases that specified the subtype of RCC, the following subtypes were demonstrated: clear cell and papillary. With regards to imaging features, the vast majority of the splenic lesion was solitary and demonstrated a heterogeneous pattern of enhancement on CT and MRI. Three patients underwent PET/CT; the splenic lesion of one patient had no metabolic activity, and in the other 2 patients, the splenic lesions were hypermetabolic.

As we can observe, imaging modalities demonstrated a pivotal role in the detection of the splenic lesions. Although not all lesions were PET/CT avid, it is a useful tool to investigate other lesions in other organs, which may change the management in these cases.

According to the literature, there is a survival benefit to an aggressive approach and a complete surgical resection of the primary tumor and metastatic sites, when technically feasible, may offer the best opportunity for cure [19]. The vast majority of the patients described in the literature underwent surgical resection. Among the reports that described the patient outcome, 2 patients died 5 and 12 months after the detection of splenic metastases and 9 patients were alive up to 2 years of follow-up.

This case report emphasizes the importance of considering splenic metastases from RCC even in patients without disseminated disease and many years after the primary tumor diagnosis. This case also stresses the need of extended follow-up since early diagnosis and treatment may improve patients’ outcome and reduce morbidity, especially considering that complete surgical resection is the main curative treatment.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

Davi dos Santos Romão and Natally Horvat contributed equally to this study. DSR, NH, MCG, ESA RBDM, PCCV, and MCCM contributed to data curation and methodology. DSR, NH, and MCCM were responsible for project administration, supervision, writing the original draft, and reviewing and editing. DSR and NH contributed equally for formal analysis and visualization. MCCM was responsible for the conceptualization of the study.


  1. S. K. Grewal, R. P. Doley, K. Roy et al., “Isolated splenic metastasis from clear cell renal carcinoma—a case report,” International Journal of Surgery Case Reports, vol. 29, pp. 44–46, 2016. View at: Publisher Site | Google Scholar
  2. C. Villarreal-Garza, S. I. Perez-Alvarez, I. R. Gonzalez-Espinoza, and E. Leon-Rodriguez, “Unusual metastases in renal cell carcinoma: a single institution experience and review of literature,” World Journal of Oncology, vol. 1, no. 4, pp. 149–157, 2010. View at: Publisher Site | Google Scholar
  3. K. Y. Lam and V. Tang, “Metastatic tumors to the spleen: a 25-year clinicopathologic study,” Archives of Pathology & Laboratory Medicine, vol. 124, no. 4, pp. 526–530, 2000. View at: Google Scholar
  4. W. B. Strum, “Remote recurrence of renal cell carcinoma,” Urology, vol. 23, no. 1, pp. 68–70, 1984. View at: Publisher Site | Google Scholar
  5. H. Ishida, K. Konno, J. Ishida et al., “Isolated splenic metastases,” Journal of Ultrasound in Medicine, vol. 16, no. 11, pp. 743–749, 1997. View at: Publisher Site | Google Scholar
  6. V. Kugel, Y. Dekel, M. Konichezky, J. Baniel, P. M. Livne, and R. Koren, “Unusual splenic metastasis from renal cell carcinoma: a case report and review of the literature,” Pathology—Research and Practice, vol. 199, no. 11, pp. 739–743, 2003. View at: Publisher Site | Google Scholar
  7. D. H. McGregor, Y. Wu, A. P. Weston, M. P. McAnaw, C. Bromfield, and M. M. Bhattatiry, “Metastatic renal cell carcinoma of spleen diagnosed by fine-needle aspiration,” The American Journal of the Medical Sciences, vol. 326, no. 1, pp. 51–54, 2003. View at: Publisher Site | Google Scholar
  8. Y. Hattori, Y. Hara, K. Matsuura, and A. Hasegawa, “A case of small cell carcinoma of kidney; solitary splenic metastasis,” Nihon Hinyokika Gakkai Zasshi, vol. 96, no. 5, pp. 572–575, 2005. View at: Google Scholar
  9. B. Ielpo, C. Mazzetti, D. Venditti, O. Buonomo, and G. Petrella, “A case of metachronous splenic metastasis from renal cell carcinoma after 14 years,” International Journal of Surgery, vol. 8, no. 5, pp. 353–355, 2010. View at: Publisher Site | Google Scholar
  10. J. A. G. Moir, G. Sen, R. Saif, B. Haugk, and J. J. French, “Isolated splenic metastasis from renal cell carcinoma: case report and review,” Case Reports in Gastroenterology, vol. 5, no. 1, pp. 166–171, 2011. View at: Publisher Site | Google Scholar
  11. T. F. Nunes, D. Szejnfeld, L. N. Miiji, and S. M. Goldman, “Isolated metachronous splenic metastasis from renal cell carcinoma after 5 years,” BMJ Case Reports, vol. 2012, 2012. View at: Publisher Site | Google Scholar
  12. L. Zhang, D. Pasquale, M. Le, R. Patel, and S. Mehdi, “Isolated splenic metastasis in a patient with two distinct genitourinary malignancies,” The Journal of Community and Supportive Oncology, vol. 13, no. 6, pp. 229-230, 2015. View at: Publisher Site | Google Scholar
  13. Z. Liu, M. W. L. Chow, A. H. C. Lua, and R. B. W. Tan, “Rare isolated synchronous splenic metastasis in a patient with type II papillary renal cell carcinoma,” AME Case Reports, vol. 2, p. 9, 2018. View at: Publisher Site | Google Scholar
  14. G. Nabi, M. S. Ansari, and A. Seth, “Early solitary splenic metastasis from adenocarcinoma of kidney,” Indian Journal of Urology, vol. 17, no. 2, pp. 175-176, 2001. View at: Google Scholar
  15. C. Shuck-Bello, G. Morales-Montor, A. Fernández-Orozco et al., “Metástasis de carcinoma de células claras de riñón a bazo,” Revista Mexicana de Urología, vol. 67, no. 2, pp. 124–128, 2007. View at: Google Scholar
  16. D. Hardikar, “Synchronous solitary metastasis in renal cell carcinoma,” Journal of Dental and Medical Science, vol. 13, no. 3, pp. 111–113, 2014. View at: Publisher Site | Google Scholar
  17. National Comprehensive Cancer Network. Kidney Cancer (Version 2.2020),
  18. B. P. Brufau, C. S. Cerqueda, L. B. Villalba, R. S. Izquierdo, B. M. González, and C. N. Molina, “Metastatic renal cell carcinoma: radiologic findings and assessment of response to targeted antiangiogenic therapy by using multidetector CT,” Radiographics, vol. 33, no. 6, pp. 1691–1716, 2013. View at: Publisher Site | Google Scholar
  19. H. B. Zaid, W. P. Parker, N. S. Safdar et al., “Outcomes following complete surgical metastasectomy for patients with metastatic renal cell carcinoma: a systematic review and meta-analysis,” Journal of Urology, vol. 197, no. 1, pp. 44–49, 2017. View at: Publisher Site | Google Scholar

Copyright © 2019 Davi dos Santos Romao et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

Article of the Year Award: Outstanding research contributions of 2020, as selected by our Chief Editors. Read the winning articles.