Splenic metastasis from recurrent chromophobe renal cell carcinoma 12 years post-nephrectomy: a case report

Abstract

Background

Renal cell carcinoma metastases to the spleen are rare. At the time of this report, only 20 cases of splenic metastases from RCC have been published in the literature. To our knowledge, our report is the first splenic metastasis from a chromophobe RCC.

Case presentation

A 44-year-old woman presented with clinical and radiological features of splenic metastasis from RCC, 12 years after radical nephrectomy for chromophobe RCC. Computed tomography, laparotomy and splenectomy revealed metastases to the spleen and retroperitoneal lymph nodes.

Conclusion

Splenic metastasis from RCC is uncommon, and rarer still from a chromophobe subtype of RCC. Surgical management of the metastasis is recommended.

1 Background

Renal cell carcinoma (RCC) is a common malignancy of the kidney, usually diagnosed serendipitously when patients undergo abdominal imaging for other conditions [1]. RCC has several histopathological subtypes which are clear cell, papillary and chromophobe RCC (chRCC). It may spread locally or present as metastatic disease to distant organs, common sites being the lungs, the liver and bones. It rarely metastasizes to the spleen [2]. We report a case of a metachronous recurrence of a left chromophobe RCC to the spleen, 12 years after excision of the primary tumor, a rarity that we could not find any report of in the English literature.

2 Case presentation

A.A. is a 44-year-old female who presented with recurrent flank pain of 2-year duration, with associated weight loss and anorexia. The pain was dull aching, insidious onset, radiated to the back, and with no known aggravating or relieving factors. There was no haematuria.

Twelve years earlier, she had similar symptoms with associated left flank swelling. Abdominal computerized tomography (CT) at the time revealed a contrast-enhancing left renal tumor. A left radical nephrectomy was performed. The resected kidney then measured 16 cm × 10 cm × 10 cm and weighed 1450 gram. The histology was that of chromophobe renal cell carcinoma (Furman's grade 3) (Fig. 1). She had no adjuvant treatment, but was reviewed regularly in the outpatient clinic in the first 5 years post-nephrectomy undergoing clinical physical examination and abdominal ultrasonography scan, on each occasion.

Fig. 1

H & E stain × 100 for (a) and × 400 for (b) showing photomicrographs of the renal tumor showing sheets of malignant cells with eosinophilic cytoplasm (a). b Some of the cells have a ‘flocculent’ eosinophilic cytoplasm while others show a perinuclear halo and binucleation (long arrows). There are a few crumpled-looking hyperchromatic nuclei while many of the cells show vesicular nuclei with prominent nucleoli (short arrows)

She never smoked tobacco cigarettes nor took alcohol. She is a clerk in a government establishment, and she had no history of prior exposure to industrial chemicals. There was no family history of similar cancer. She is married and has 2 children, both delivered through caesarean sections. She was not hypertensive and didn’t have diabetes mellitus.

Physical examination revealed an emaciated middle-aged woman. She was pale, but afebrile, anicteric and with no peripheral lymph node enlargement. Systemic examination findings were normal aside left subcostal scar of previous nephrectomy and scar of previous Pfannenstiel incision. A clinical diagnosis of a recurrent left renal cell carcinoma was made.

Abdominal computerized tomography scan revealed a fairly rounded heterogenous, contrast enhancing mass with mixed density in the left hypochondrium, appearing to extend from the left renal bed, measuring 7.5 × 7.6 × 7.1 cm. The mass had multiple central areas of hypodensity but no calcification. It appeared to be continuous with the spleen. There were no lymphadenopathies or ascites (Fig. 2).

Fig. 2

a Axial CT of the abdomen showing contrast enhancing left hypochondrial mass and b. coronal section of the same abdomen (solid arrows)

She was anemic with haematocrit of 29%, but had normal white cells and platelet counts. Her serum electrolytes, urea and creatinine, liver function test and clotting profile, were normal.

Following pre-operative optimization of her clinical condition including correction of anemia with red cell transfusion, she underwent exploratory laparotomy through an upper abdominal midline incision. A careful but daunting adhesiolysis was performed following which the following findings were appreciated: no peritoneal seedlings nor ascites or liver metastasis, left renal bed grossly free of tumor, an enlarged spleen with a centrally placed mass measuring about 5 cm × 4 cm, (Fig. 3), an enlarged retroperitoneal lymph node, and normal right kidney. Total splenectomy and excision of the enlarged retroperitoneal lymph node was then carried out. During splenectomy, the spleen was mobilized gently to prevent breaching of its capsule and tumor spillage. Adequate haemostasis was secured. Estimated blood loss was about 360 ml.

Fig. 3

Gross picture of the spleen with a cystic cavity containing tumor (arrow) and necrotic material. a focal area of rupture by the tumor is seen (arrowhead)

On account of persistent unexplained intra-operative hypotension that extended to immediate post-operative period, and clinical features in keeping with adult respiratory distress syndrome, she was admitted into the intensive care unit for ionotropic support and mechanical ventilation. She was extubated on the 5th post-operative day and transferred to the ward, where she had polyvalent vaccine for Streptococcus pneumoniae, Neisseria meningitidis and Haemophilus influenza during her recovery. She made steady clinical improvement culminating in her discharge from in-hospital care on post-operative day 24. Histology of the splenic mass (Fig. 4) and retroperitoneal lymph node (Fig. 5) revealed a metastatic renal cell carcinoma.

Fig. 4

H & E stain × 100 showing Photomicrographs of metastatic chromophobe renal cell carcinoma. The cells are similar to the primary tumor in the kidneys. There is a capsular rupture with nests of tumor cells outside of the splenic capsule (arrow)

Fig. 5

H & E stain × 100 showing sections of the lymph node with tumor infiltration into blood vessels (arrows)

She has had 44 Gy of external beam radiotherapy to the renal and splenic bed in 22 fractions. Planned targeted therapy with sorafenib could not be given due to unaffordability of the drug by the patient. Abdomino-pelvic ultrasonography and CT scan done at 6 months after the laparotomy showed no evidence of tumor recurrence. Her follow-up period—now at 12 months—has remained uneventful. Informed consent was obtained from the patient to write and publish this case report.

3 Discussion

RCC is a common type of renal cancer, accounting for about 80% of primary renal cancers [3]. Chromophobe histologic subtype accounts for 5% of RCCs, and they have better prognosis than the more common clear cell subtype [4]. The initial clinical and radiologic picture of the index case was suggestive of a local recurrence of the chromophobe renal cell carcinoma of 12 years earlier. The long time to recurrence is consistent with the biology of chromophobe RCC. Ismail et al. previously described a case of a 15-year local recurrence of chromophobe RCC in a 57-year-old woman who had T1b disease [5]. Our patient, however, presented as a metastasis in a splenic mass.

Yip et al. in a retrospective analysis found that, of 4,970 patients with metastatic RCCs, only 2.2% were of the chromophobe subtype [6]. RCCs would commonly metastasize to the lungs, bone, liver, and adrenal gland, while chRCC more commonly metastasizes to the liver [7]. Splenic metastases are uncommon. Theories explaining the relative rarity of splenic metastasis include: mechanical factors impeding implantation of tumor emboli such as constant flow, sharp angle of splenic artery branching from the celiac trunk, lack of afferent lymphatic vessels and the anti-tumor activity of the lymphoid tissue in the spleen [8].

A literature search on PubMed and MedLine with keywords such as splenic metastases, renal/kidney RCC metastases to the spleen was performed. At the time of writing this report, and to the best of our knowledge, there have been only 20 published reports of RCC metastases to the spleen, in the literature (Table 1) [9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27]. Of the reports, most primaries were clear cell RCCs, only a few were of the papillary RCC subtype. To our knowledge, our report if eventually published will be the first splenic metastasis from chromophobe RCC in the English literature, hence the uniqueness of this case report.

Table 1 Literature review of published case reports of splenic metastases from RCC

Total or partial splenectomy are surgical options for solitary splenic metastasis, especially in symptomatic patients with pain like the index case, and to prevent tumor rupture with bleeding, a potential but rare complication, with resection alone being sometimes successful. The rationale for total splenectomy in this case was the central location of the tumor in the spleen. Routine pre-operative preparation for total splenectomy, including pre-operative vaccinations, was not done because we thought the recurrent tumor was at the renal bed; splenic involvement was detected only at surgery. She, however, had the necessary vaccinations within 2 weeks of the splenectomy, with the plan for subsequent booster doses in future as recommended.

Though there is availability of local expertise and equipment for laparoscopic splenectomy, this was not considered in this case, again because we did not consider splenectomy as a component of the operation in the planning stage. Even if splenectomy was planned, previous surgeries with their attendant adhesions in a non-virgin abdomen would have contraindicated laparoscopic approach.

Some authors have advocated employing the histologic appearance, the binucleation, ‘raisinoid’ nuclear appearance and perinuclear halo, in making the diagnosis of the tumor [29]. Some of these features are seen in the index case, both in the primary renal tumor as well as in the metastatic tumor. In addition to the well-known histological appearance for the diagnosis of chromophobe RCC as advocated by some authors, a few panels of immunomarkers such as CD 117 and CK 7 may be used to confirm the diagnosis and distinguish it from the benign tumor, oncocytoma. We were, however, unable to perform immunohistochemical staining of the tissue blocks due to logistical difficulties–a limitation of this case report.

The prognosis of chRCC is reported to be good, with a 10-year survival rate of 100% for localized (T1) chRCC [4]. However, metastatic chRCC has been shown to have an overall survival rate of 23.8 months in a study by Yip et al. In the same study, the overall response rate of metastatic chRCC to first-line targeted therapy (Sunitinib, Sorafenib, Everolimus) was 21% [6]. Our patient would be followed up with this information on good prognosis in mind.

4 Conclusion

Splenic metastasis from RCC is uncommon, and rarer still from a chromophobe subtype of RCC. Surgical management of the metastasis is recommended, along with adjuvant radiotherapy to the splenic bed, and targeted therapy where available.