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194

Ces Urol 2016; 20(3): 192–194

VIDEO

(67.6% of all pRCCs, 6.1% of all renal tumours), the

others were pRCC type 2 (14/148 – 95%), onco‑

cytic pRCC – (opRCC (19–12.8%) and not otherwise

specified (NOS) – (15–10.1%). Oncocytic pRCC has

not yet been officially recognized by WHO clas‑

sification 2016 .

Results:

The preferred method in all groups of

pRCC was resection – in pRCC type 1 up to 80.7%.

For comparison, the ratio of resections performed

during this period of 9 years (1629 tumours) was

48.4%. WHO (ISUP) Grade 1 was most represented

in pRCC type 1. In other groups, Grade 3 was the

most common grade – in pRCC type 2 up to 78.6%.

3-years progression-free survival was 97.1% in our

study, in pRCC type 2 (44,1%), opRCC (85,4%), NOS

(69,9%) (4). The disease progression was observed

in 3 patients with a histologically verified pRCC1. All

3 patients had undergone an open nephrectomy.

In 2 of the cases due to large tumours, 145 and

180mm (stage cT2b and cT3a) and in one case

a tumour duplicity had been diagnosed (tumour

of the sigma). In histologically verified pRCC2, a cy‑

toreductive operation was performed in 2 cases of

progression. In 3 further cases we noted progres‑

sion; of which 2 were after resection and one after

nephrectomy.

Our video presentation presents a 44years-old,

obese man (BMI 30.8) with a palpable renal tumour

at the lower pole of the left kidney. Tumour size

was 10 cm at the tumour´s widest part according

to CT. The tumour has extrarenal growth, regular

spherical shape, stage cT2a. R.E.N.A.L. score 9a

(6). Translumbal resection was performed, time of

clamping of the hilum 7 minutes and blood loss

100 ml. The tissue sample was ochre coloured,

typically fragile, 639 g and histologically it was

verified as a pRCC type 2, without interference

anywhere in the resection line. The patient is so far

without recurrence of the kidney tumour (period

of monitoring – 32.4 months), but unfortunately

he is being treated for metastatic prostatic cancer.

Conclusion:

Papillary renal cell carcinoma is

possible in most cases safely treated by resection

thanks to its typical extrarenal growth, in individual

cases also in stage cT2a. It is necessary to closely

monitor patients after resection with histologi‑

cally verified pRCC type 2 tumours for their proven

higher potential of malignancy.

KEY WORDS

Grade, papillary renal cell carcinoma, obesity, prog‑

nosis, resection.

LITERATURA

1. Hora M, Hes O, Boudová L, et al.

Papilární renální karcinom. Ces Urol 2002; 6: 26–31.

2. Hora M, Hes O, Klečka J, et al.

Rupture of papillary renal cell carcinoma. Scand J Urol Nephrol 2004;

38: 481–484.

3. Delahunt B, Eble JN, McCredie MRE, Bethwaite PB, Stewart JH, Bilous AM.

Morphologic typing of

papillary renal cell carcinoma: Comparison of growth kinetics and patient survival in 66 cases. Hum Pathol

2001; 32: 590–595.

4. Procházková K, Staehler M, Travníček I, et al.

Morphological Characterization of Papillary Renal Cell

Carcinoma Type 1, the Efficiency of its Surgical Treatment. Urol Inter 2016 in print, DOI: 10.1159/000448434

5. Delahunt B, Eble JN.

Papillary renal cell carcinoma: a clinicopathologic and immunohistochemical study

of 105 tumors. Mod Pathol Off J U S Can Acad Pathol Inc 1997; 10: 537–544.

6. Kutikov A, Uzzo RG.

The R.E.N.A.L. Nephrometry Score: A Comprehensive Standardized System for

Quantitating Renal Tumor Size, Location and Depth. J Urol 2009; 182: 844–853.