Overview

Classification

The pathology report plays a vital role in the management of renal cell carcinoma (RCC).1 It provides the urologist and oncologist with an accurate diagnosis and prognostic information, which facilitates appropriate decisions on further patient care, such as the requirement for adjuvant treatment (e.g. with targeted agents) and development of a suitable follow-up schedule. Retrieval of the maximum amount of information requires correct handling of the tumour specimen at all time points and relies on collaboration between pathologists and clinicians, urologists and oncologists.

For a long time, only a few cellular subtypes of RCC were recognized. However, the advent of immunohistochemical methods, together with genetic studies, has made it possible to recognize multiple cell subtypes with both genetic and biological differences. This is reflected in the WHO 2004 classification (Table 3.1),2,3 based on histological and genetic features, which recognizes a growing number of relevant clinico pathological subtypes with differing histogenesis and prognosis.

Malignant tumours Benign tumours
Clear-cell RCC Paplllary adenoma
Multilocular cystic clear-cell RCC Oncocytoma
Papillary RCC  
Chromophobe RCC  
Carcinoma of the collecting ducts of Bellini  
Renal medullary carcinoma  
Xp11 translocation carcinomas  
Mucinous tubular and spindle cell carcinoma  
Carcinoma associated with neuroblastoma  
RCC, unclassified  

Table 3.1 WHO histological classification of renal cell tumours.2,3 Adapted from Eble et al. 2004 with kind permission from Springer.
RCCs may be sporadic or inherited. 

Primary tumour (T)
TX Primary tumour cannot be assessed
T0 No evidence of primary tumour
T1 Tumour 7 cm or less in greatest dimension, limited to the kidney
T1a Tumour 4 cm or less in greatest dimension, limited to the kidney
T1b Tumour more than 4 cm but not more than 7 cm in greatest dimension, limited to the kidney
T2 Tumour more than 7 cm in greatest dimension, limited to the kidney
T2a Tumour more than 7 cm but less than or equal to 10 cm in greatest dimension, limited to the kidney
T2b Tumour more than 10 cm, limited to the kidney
T3 Tumour extends into major veins or perinephric tissues but not into the ipsilateral adrenal gland and not beyond Gerota’s fascia
T3a Tumour grossly extends into the renal vein or its segmental (muscle-containing) branches, or tumour invades perirenal and/or renal sinus fat but not beyond Gerota’s fascia
T3b Tumour grossly extends into the vena cava below the diaphragm
T3c Tumour grossly extends into vena cava above the diaphragm or invades the wall of the vena cava
T4 Tumour invades beyond Gerota’s fascia (including contiguous extension into the ipsilateral adrenal gland)
Regional lymph nodes (N)
NX Regional lymph nodes cannot be assessed
N0 No regional lymph node metastasis
N1 Metastasis in regional lymph node(s)
Distant metastasis (M)
M0 No distant metastasis
M1 Distant metastasis

Table 3.5 The 2010 TNM classification

This information has been provided with the kind permission of Vincent Molinié,Mathilde Sibony, Jérôme Couturier and Annick Vieillefond

References:
1. Kirkali Z, Algaba F, Scarpelli M et al. What does the urologist expect from the pathologist (and what can the pathologists give) in reporting on adult kidney tumour specimens? Eur Urol 2007;51:1194–1201.
2. Lopez-Beltran A, Scarpelli M, Montironi R, Kirkali Z. 2004 WHO classification of the renal tumors of the adults. Eur Urol 2006;49:798–805.
3. Eble JN, Sauter G, Epstein JI, Sesterhenn IA. World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of the Urinary System and Male Genital Organs. Lyon, France: IARC Press; 2004.