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20 Turkish Journal of Cancer Vol.32/ No. 1/2002 Squamous cell carcinoma located in the renal caliceal system: A case report and review of the literature AYHAN KARABULUT 1 , LEVENT EMİR 1 , MEHMET GÖNÜLTAŞ 2 , NAZMİ İNCEL 1 , CANKON GERMİYANOĞLU 1 , DEMOKAN EROL 1 Departments of 1 Urology and 2 Pathology, The Ministry of Health Ankara Education and Research Hospital, Ankara-Turkey Squamous cell carcinoma of the urinary tract is a very rarely encountered tumor. It is more frequently reported in bladder and male urethra than in renal pelvis. With the addition of new cases in the literature, the impact of its features, such as the location and the stage of the tumor, on the outcome will be highlighted. Here, we present a case with renal squamous cell carcinoma located in the upper caliceal system and discuss it in the light of current literature. [Turk J Cancer 2002;32(1):20-24] Key words: Squamous cell, kidney, carcinoma Primary neoplasms of the renal collecting system are uncommon, accounting for only 4-5% of all urothelial tumors (1,2). The transitional cell type is the most frequently diagnosed (85% to 95%), followed by squamous cell carcinoma (6% to 15%) and adenocarcinoma (7%) (3,4). In the present paper, we report a 62 years old women who had lithiasis and squamous cell carcinoma in her right non-functioning kidney. Case report A 62 year old female patient presented with intermittent, mild, right flank pain. She had a history of urolithiasis for a long time. Physical examination revealed a slight tenderness on right costovertebral angle and a palpable mass on upper right quadrant of abdomen. Complete blood count, erythrocyte sedimentation rate, biochemical analysis and urinalysis were all within the normal ranges. Intravenous urogram revealed a non-functioning right kidney and a 22x20 mm radioopacity located at the right renal area. Ultrasonography revealed an obstructing calculi located in the renal pelvis and a solid mass in the upper pole calyx. Computed tomography demonstrated a huge, non- functioning, hydronephrotic right kidney with a calculi of diameters 23x21 mm located in the renal pelvis and a solid mass of approximately 25x21 mm in size, located at the inner surface of the upper dilated calyx (Figure 1). There was an adipose tissue obliteration between the liver and the adjacent right kidney.

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Page 1: Squamous cell carcinoma located in the renal caliceal ... · PDF fileSquamous cell carcinoma located in the renal caliceal system: A case report and review of the literature AYHAN

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Turkish Journal of CancerVol.32/ No. 1/2002

Squamous cell carcinoma locatedin the renal caliceal system: A case report

and review of the literatureAYHAN KARABULUT1, LEVENT EMİR1, MEHMET GÖNÜLTAŞ2,NAZMİ İNCEL1, CANKON GERMİYANOĞLU1, DEMOKAN EROL1

Departments of 1Urology and 2Pathology, The Ministry of Health AnkaraEducation and Research Hospital, Ankara-Turkey

Squamous cell carcinoma of the urinary tract is a very rarelyencountered tumor. It is more frequently reported in bladder andmale urethra than in renal pelvis. With the addition of new casesin the literature, the impact of its features, such as the locationand the stage of the tumor, on the outcome will be highlighted.Here, we present a case with renal squamous cell carcinomalocated in the upper caliceal system and discuss it in the light ofcurrent literature. [Turk J Cancer 2002;32(1):20-24]

Key words: Squamous cell, kidney, carcinoma

Primary neoplasms of the renal collecting system are uncommon,accounting for only 4-5% of all urothelial tumors (1,2). The transitional cell typeis the most frequently diagnosed (85% to 95%), followed by squamous cellcarcinoma (6% to 15%) and adenocarcinoma (7%) (3,4). In the present paper,we report a 62 years old women who had lithiasis and squamous cell carcinomain her right non-functioning kidney.

Case report

A 62 year old female patient presented with intermittent, mild, right flankpain. She had a history of urolithiasis for a long time. Physical examinationrevealed a slight tenderness on right costovertebral angle and a palpable masson upper right quadrant of abdomen. Complete blood count, erythrocytesedimentation rate, biochemical analysis and urinalysis were all within thenormal ranges. Intravenous urogram revealed a non-functioning right kidneyand a 22x20 mm radioopacity located at the right renal area. Ultrasonographyrevealed an obstructing calculi located in the renal pelvis and a solid mass inthe upper pole calyx. Computed tomography demonstrated a huge, non-functioning, hydronephrotic right kidney with a calculi of diameters 23x21 mmlocated in the renal pelvis and a solid mass of approximately 25x21 mm in size,located at the inner surface of the upper dilated calyx (Figure 1). There was anadipose tissue obliteration between the liver and the adjacent right kidney.

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KARABULUT et al. 21

Fig 1. Tomographic view of intraluminal solid mass in the right kidney

On the basis of these findings a radical right nephroureterectomy wasperformed. The convalescence was uneventful.

Histopathologic examination revealed a tumoral tissue with atypicalsquamous epithelial cells and intensive necrotic areas which invaded the renalparenchyma (Figures 2 and 3).

Fig 2. Tumoral tissue with atypical squamous epithelial cells (H&E X100)

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RENAL SQUAMOUS CELL CARCINOMA22

Figure 3. Intensive necrotic areas and atypical squamous epithelial cells whichinvaded the renal parenchyma (H&E X20)

The intact renal tissue showed tubular dilatation, thyroidisation andlymphocytic infiltration that were all consistent with pyelonephritis. Tumorinvaded renal capsule and fascia of Gerota but not beyond the perirenaladipose tissue. No metastasis was detected in the hilar lymph nodes. Thepatient is under the follow-up for 4 months with no evidence of relapse ormetastasis of the disease.

Discussion

Primary squamous cell carcinoma of the renal collecting system is a veryrare entity. The incidence of renal squamous cell carcinoma among malignantrenal tumors ranged widely from 0.5% to 8% in the previous reports (5,6). Ingeneral, these tumors are highly aggressive and are at high stage whendetected and can be expected to have a poor clinical course.

The lack of characteristic presentation like hematuria, pain and palpablemass causes delay in diagnosis. Most of the detected tumors are histologicallyhigh grade, 84% of the tumors were locally advanced or metastatic (7).

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KARABULUT et al. 23

Squamous cell carcinoma of the renal pelvis is often associated with phenacetinconsumption, chronic renal calculi or infection. The incidence of co-existingurinary stone was reported in a wide range between 18% (6) and 100% (5).Squamous metaplasia invades mucosa adjacent to the carcinoma in 17% to33% of the patients (8). Whether the occurrence of squamous metaplasia is dueto the presence of the calculus that leads ultimately to the development ofcarcinoma or existence of squamous cell carcinoma causes the formation ofcalculus is not clear yet. This dilemma is particularly valid for the co-existenceof the tumor and calculus at the renal pelvis. As renal squamous cell carcinomais frequently associated with infected staghorn calculi existing for a longduration, it is recommended for the patients with renal stone disease who don’tneed intervention or patients under extracorporeal shock wave lithotripsytreatment or patients with non-functioning kidney due to stone disease to becarefully examined with imaging modalities (9).

The tumor can be documented by conventional radiological imagingmodalities. Filling defects or obstructive lesions in the renal pelvis byintravenous/retrograde urography or detection of a solid mass byultrasonography can be the signs of the tumor (10). Tomographic imagingreveals these findings more specifically (10,11).

Recently in a retrospective study of Lee et al (9), 15 patients with squamouscell carcinoma of the kidney were classified into two groups according tolocalisation of the tumors as central and peripheral type. They stated that thecentral renal squamous cell carcinoma presents more intraluminal componentsand is usually associated with lymph node metastasis whereas peripheral renalsquamous cell carcinoma presents with prominent renal parenchymalthickening and might invade the perirenal fat tissue before lymph node ordistant metastasis could be identified. The survival of patients with central renalsquamous cell carcinoma was reported to be significantly shorter than thosewith peripheral renal squamous cell carcinoma.

In the report of Nativ et al (7), patients with renal squamous cell carcinomawere divided into three groups on the basis of tumor staging criterias outlinedby Peterson (12). Nativ et al reported that patients with locally invasive renalsquamous cell carcinomas had 1 and 2 year-survival rates of 33% and 22%,respectively. They have also reported that the treatment modalities likenephrectomy, nephroureterectomy, adjuvant radiotherapy or chemotherapy,irrespective of tumor stage, did not affect the survival of the patients.

The current primary treatment of renal squamous cell carcinoma isnephroureterectomy. If metastasis develops, adjuvant chemotherapy orirradiation has little effect on the unfavourable prognosis (10).

The case that we mention here is consistent with the peripheral type renalsquamous cell carcinoma as reported by Lee et al (9). The tumor was locallyadvanced like most of the tumors in the literature. The co-existence of renalcalculus and renal squamous cell carcinoma was also present in this case.Patients with renal stone disease who don’t need intervention or patients underextracorporeal shock wave lithotripsy treatment or patients with non-functioningkidney due to stone disease must be carefully examined with imagingmodalities and by this way the early detection of the tumor may provide a betteroutcome for the patients.

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RENAL SQUAMOUS CELL CARCINOMA24

Despite the tumor of our patient has invaded the fascia of Gerota, we are inan expectation of a better survival with respect to the central type renalsquamous cell carcinoma. We decided to follow-up the patient until theevidence of metastatic disease would be demonstrated. We are planning tostart a combination chemotherapy including methotrexate, cisplatin andbleomycin as reported by Corral et al (13) recently if the signs of metastaticdisease are revealed. Corral reported a high but short lived overall responserate with this chemotherapy regimen.

References

1. Murphy DM, Zincke H, Furlow WL. Primary grade I transitional cellcarcinoma of the renal pelvis and ureter. J Urol 1980;123:629-31.

2. Murphy DM, Zincke H, Furlow WL. Management of high grade transitionalcell cancer of the upper urinary tract. J Urol 1981;125:25-9.

3. Latham HS, Kay S. Malignant tumors of the renal pelvis. Surg GynecolObstet 1974;138:613-22.

4. Utz DC, Mc Donalt JR. Squamous cell carcinoma of the kidney. J Urol1957;78:540-52.

5. Li MK, Cheung WL. Squamous cell carcinoma of the renal pelvis. J Urol1987;138:269-71.

6. Blacher EJ, Johnson DE, Abdul-Karim FW, et al. Squamous cell carcinomaof renal pelvis. Urology 1985;25:124-6.

7. Nativ O, Reiman HM, Lieber MM, et al. Treatment of primary squamous cellcarcinoma of the upper urinary tract. Cancer 1991;68:2575-8.

8. Melamed MR, Reuter VE. Pathology and staging of urothelial tumors of thekidney and ureter. Urol Clin North Am 1993;20:333-47.

9. Lee TY, Ko JF, Wan YL, et al. Renal squamous cell carcinoma: CT findingsand clinical significance. Abdom Imaging 1998;23:203-8.

10. Messing MM, Catalona W. Urothelial tumors of the urinary tract. In: WalshPC, Retik AB, Vaughan ED, Wein AJ, editors. Campbell’s Urology.Philadelphia: WB Saunders company, 1998: 2327-410.

11. Narumi Y, Sato T, Hori S, et al. Squamous cell carcinoma of theuroepithelium: CT evaluation. Radiology 1989;173:853-6.

12. Peterson RO. Urologic pathology. Philadelphia: JB Lippincott, 1986;196-205.13. Corral DA, Sella A, Pettaway CA, et al. Combination chemotherapy for

metastatic or locally advanced genitourinary squamous cell carcinoma: Aphase II study of methotrexate, cisplatin and bleomycin. J Urol1998;160:1770-4.