Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Review Article
  • Published:

A practical guide to bladder cancer pathology

Key Points

  • Providing details of a patient's clinical history to the pathologist is crucial to ensure correct assessment and reporting, especially if the patient received previous tumour-related treatments or has an ongoing inflammatory response

  • Providing urothelial tumour staging data to the treating clinician is essential, as patient prognosis and treatment selection are stage-dependent

  • Substaging of pT1 tumours has been introduced to the 2016 WHO Classification of Tumours of the Urinary System and Male Genital Organs blue book, and the International Collaboration on Cancer Reporting suggests several detailed models for recording the extent of invasion

  • According to the 2016 WHO classification, urothelial carcinoma can be categorized into low-grade and high-grade tumours; however, consensus guidance on how to report heterogeneous lesions is still lacking

  • No widely accepted standards exist for gross handling and examination of cystectomy and lymphadenectomy specimens, and only few protocols are available, leaving handling and sampling to the discretion of individual pathologists

  • Abundant data on the molecular characteristics of bladder cancer have been published, but how to integrate these findings to improve pathological assessment and patient management remains unclear; a consensus for a panel of markers is needed

Abstract

Pathological assessment of bladder cancer is becoming an increasingly complex task owing to the growing availability of molecular data for different histological subtypes and the appreciation of their importance in determining outcomes of neoadjuvant chemotherapy. Urologists are aware of the need to closely collaborate with pathologists, and comprehensive sharing of information is crucial to achieve optimal patient management. Numerous steps towards this goal have been made during the past years. Important advances in the assessment and reporting of grading and staging, especially substaging of pT1 urothelial carcinomas, have been made. As part of the International Collaboration on Cancer Reporting (ICCR), an international expert group has suggested worldwide reporting standards for urothelial lesions. Nevertheless, several issues remain unresolved, for example, regarding the reporting of heterogeneous lesions and substaging as well as the gross handling and the reporting for lymphadenectomy specimens. During the past few years, major insights have been gained into the molecular changes that occur during bladder cancer development, but a consensus on how to integrate these data into daily practice has not been achieved.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: Grade classification of urothelial carcinoma.
Figure 2: Staging of urothelial carcinoma.
Figure 3: Challenges in assessing tumour invasion and staging.
Figure 4: Tumour staging in cystectomy samples.
Figure 5: Schematic representation of intrinsic subtypes of bladder cancer.

Similar content being viewed by others

References

  1. Mokdad, A. H. et al. Trends and patterns of disparities in cancer mortality among US counties, 1980–2014. JAMA 317, 388–406 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  2. Weijers, Y., Arentsen, H. C., Arends, T. J. H. & Witjes, J. A. Management of low-risk and intermediate-risk non-muscle-invasive bladder carcinoma. Hematol. Oncol. Clin. North Am. 29, 219–225, vii (2015).

    Article  PubMed  Google Scholar 

  3. Chappidi, M. R. et al. Causes, timing, hospital costs and perioperative outcomes of index versus nonindex hospital readmissions after radical cystectomy: implications for regionalization of care. J. Urol. 197, 296–301 (2017).

    Article  PubMed  Google Scholar 

  4. Welty, C. J. et al. The Cancer of the Bladder Risk Assessment (COBRA) score: Estimating mortality after radical cystectomy. Cancer 123, 4574–4582 (2017).

    Article  CAS  PubMed  Google Scholar 

  5. Alfred Witjes, J. et al. Updated 2016 EAU guidelines on muscle-invasive and metastatic bladder cancer. Eur. Urol. 71, 462–475 (2017).

    Article  CAS  PubMed  Google Scholar 

  6. Babjuk, M. et al. EAU Guidelines on non-muscle-invasive urothelial carcinoma of the bladder: update 2016. Eur. Urol. 71, 447–461 (2017).

    Article  PubMed  Google Scholar 

  7. Hansel, D. E. et al. A contemporary update on pathology standards for bladder cancer: transurethral resection and radical cystectomy specimens. Eur. Urol. 63, 321–332 (2013).

    Article  PubMed  Google Scholar 

  8. Amin, M. B. et al. Update for the practicing pathologist: The International Consultation On Urologic Disease-European association of urology consultation on bladder cancer. Mod. Pathol. 28, 612–630 (2015).

    Article  PubMed  Google Scholar 

  9. Chandra, A., Griffiths, D. & McWilliam, L. J. Best practice: gross examination & sampling of surgical specimens from the urinary bladder. J. Clin. Pathol. 63, 475–479 (2010).

    Article  PubMed  Google Scholar 

  10. International Collaboration on Cancer Reporting. Welcome to the International Collaboration on Cancer Reporting (ICCR). ICCR http://www.iccr-cancer.org/ (2018).

  11. Humphrey, P. A., Moch, H., Cubilla, Ulbright, A. L., T. M. & Reuter, V. E. The 2016 WHO classification of tumours of the urinary system and male genital organs — part B: prostate and bladder tumours. Eur. Urol. 70, 106–119 (2016).

    Article  PubMed  Google Scholar 

  12. World Health Organization Classification of Tumours. Pathology and genetics of tumours of the urinary system and male genital organs (IARC Press, Lyon, 2004).

  13. Epstein, J. I., Amin, M. B., Reuter, V. R. & Mostofi, F. K. The World Health Organization/International Society of Urological Pathology consensus classification of urothelial (transitional cell) neoplasms of the urinary bladder. Bladder Consensus Conference Committee. Am. J. Surg. Pathol. 22, 1435–1448 (1998).

    Article  CAS  PubMed  Google Scholar 

  14. Mostofi, F. K., Sobin, L. H. & Torloni, H. Histological Typing of Urinary Bladder Tumours (World Health Organization, Geneva, 1973).

    Google Scholar 

  15. Sylvester, R. J. et al. Predicting recurrence and progression in individual patients with stage Ta T1 bladder cancer using EORTC risk tables: a combined analysis of 2596 patients from seven EORTC trials. Eur. Urol. 49, 466–477 (2006).

    Article  PubMed  Google Scholar 

  16. Kim, J. K. et al. Papillary urothelial neoplasm of low malignant potential (PUNLMP) after initial TUR-BT: comparative analyses with noninvasive low-grade papillary urothelial carcinoma (LGPUC). J. Cancer 8, 2885–2891 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  17. Hu, Z., Mudaliar, K., Quek, M. L., Paner, G. P. & Barkan, G. A. Measuring the dimension of invasive component in pT1 urothelial carcinoma in transurethral resection specimens can predict time to recurrence. Ann. Diagn. Pathol. 18, 49–52 (2014).

    Article  PubMed  Google Scholar 

  18. McKenney, J. K., Gomez, J. A., Desai, S., Lee, M. W. & Amin, M. B. Morphologic expressions of urothelial carcinoma in situ: a detailed evaluation of its histologic patterns with emphasis on carcinoma in situ with microinvasion. Am. J. Surg. Pathol. 25, 356–362 (2001).

    Article  CAS  PubMed  Google Scholar 

  19. Cancer Genome Atlas Research Network. Comprehensive molecular characterization of urothelial bladder carcinoma. Nature 507, 315–322 (2014).

  20. Rosenthal, D. L., Wojcik, E. M. & Kurtycz, D. F. I. The Paris System for Reporting Urinary Cytology (Springer, 2016).

    Book  Google Scholar 

  21. Reis, L. O. et al. Significance of a minor high-grade component in a low-grade noninvasive papillary urothelial carcinoma of bladder. Hum. Pathol. 47, 20–25 (2016).

    Article  PubMed  Google Scholar 

  22. Cheng, L. et al. Cancer heterogeneity and its biologic implications in the grading of urothelial carcinoma. Cancer 88, 1663–1670 (2000).

    Article  CAS  PubMed  Google Scholar 

  23. Gofrit, O. N. et al. Mixed high and low grade bladder tumors — are they clinically high or low grade? J. Urol. 191, 1693–1696 (2014).

    Article  PubMed  Google Scholar 

  24. Downes, M. R. et al. Analysis of papillary urothelial carcinomas of the bladder with grade heterogeneity: supportive evidence for an early role of CDKN2A deletions in the FGFR3 pathway. Histopathology 70, 281–289 (2017).

    Article  PubMed  Google Scholar 

  25. Kirkali, Z. et al. Bladder cancer: epidemiology, staging and grading, and diagnosis. Urology 66, 4–34 (2005).

    Article  PubMed  Google Scholar 

  26. van Rhijn, B. W. G. et al. Recurrence and progression of disease in non-muscle-invasive bladder cancer: from epidemiology to treatment strategy. Eur. Urol. 56, 430–442 (2009).

    Article  PubMed  Google Scholar 

  27. Williams, S. B. & Kamat, A. M. Optimum management of non-muscle-invasive micropapillary variant urothelial carcinoma: possibility for missed chance of cure? BJU Int. 118, 349–350 (2016).

    Article  PubMed  Google Scholar 

  28. Compérat, E. et al. An interobserver reproducibility study on invasiveness of bladder cancer using virtual microscopy and heatmaps. Histopathology 63, 756–766 (2013).

    Article  PubMed  Google Scholar 

  29. Herr, H. W., Donat, S. M. & Dalbagni, G. Can restaging transurethral resection of T1 bladder cancer select patients for immediate cystectomy? J. Urol. 177, 75–79 (2007).

    Article  PubMed  Google Scholar 

  30. van Rhijn, B. W. G. et al. Pathological stage review is indicated in primary pT1 bladder cancer. BJU Int. 106, 206–211 (2010).

    Article  PubMed  Google Scholar 

  31. Orsola, A. et al. Initial high-grade T1 urothelial cell carcinoma: feasibility and prognostic significance of lamina propria invasion microstaging (T1a/b/c) in BCG-treated and BCG-non-treated patients. Eur. Urol. 48, 231–238 (2005).

    Article  CAS  PubMed  Google Scholar 

  32. Kassouf, W. et al. Recommendations for the improvement of bladder cancer quality of care in Canada: a consensus document reviewed and endorsed by Bladder Cancer Canada (BCC), Canadian Urologic Oncology Group (CUOG), and Canadian Urological Association (CUA), December 2015. Can. Urol. Assoc. J. 10, E46–E80 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  33. Bol, M. G. et al. Reproducibility and prognostic variability of grade and lamina propria invasion in stages Ta, T1 urothelial carcinoma of the bladder. J. Urol. 169, 1291–1294 (2003).

    Article  PubMed  Google Scholar 

  34. Lopez-Beltran, A. & Cheng, L. Stage pT1 bladder carcinoma: diagnostic criteria, pitfalls and prognostic significance. Pathology 35, 484–491 (2003).

    Article  PubMed  Google Scholar 

  35. Cox, R. & Epstein, J. I. Large nested variant of urothelial carcinoma: 23 cases mimicking von Brunn nests and inverted growth pattern of noninvasive papillary urothelial carcinoma. Am. J. Surg. Pathol. 35, 1337–1342 (2011).

    Article  PubMed  Google Scholar 

  36. Brimo, F. et al. Inverted urothelial carcinoma: a series of 12 cases with a wide morphologic spectrum overlapping with the large nested variant. Hum. Pathol. 46, 1506–1513 (2015).

    Article  PubMed  Google Scholar 

  37. Cheng, L., Montironi, R., Davidson, D. D. & Lopez-Beltran, A. Staging & reporting of urothelial carcinoma of the urinary bladder. Mod. Pathol. 22 (Suppl. 2), S70–S95 (2009).

    Article  PubMed  Google Scholar 

  38. Drew, P. A., Furman, J., Civantos, F. & Murphy, W. M. The nested variant of transitional cell carcinoma: an aggressive neoplasm with innocuous histology. Mod. Pathol. 9, 989–994 (1996).

    CAS  PubMed  Google Scholar 

  39. Rouprêt, M. et al. Prognostic interest in discriminating muscularis mucosa invasion (T1a versus T1b) in nonmuscle invasive bladder carcinoma: French national multicenter study with central pathology review. J. Urol. 189, 2069–2076 (2013).

    Article  PubMed  Google Scholar 

  40. Younes, M., Sussman, J. & True, L. D. The usefulness of the level of the muscularis mucosae in the staging of invasive transitional cell carcinoma of the urinary bladder. Cancer 66, 543–548 (1990).

    Article  CAS  PubMed  Google Scholar 

  41. Orsola, A. et al. Reexamining treatment of high-grade T1 bladder cancer according to depth of lamina propria invasion: a prospective trial of 200 patients. Br. J. Cancer 112, 468–474 (2015).

    Article  CAS  PubMed  Google Scholar 

  42. De Marco, V. et al. Prognostic role of substaging in T1G3 transitional cell carcinoma of the urinary bladder. Mol. Clin. Oncol. 2, 575–580 (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  43. Cheng, L., Weaver, A. L., Neumann, R. M., Scherer, B. G. & Bostwick, D. G. Substaging of T1 bladder carcinoma based on the depth of invasion as measured by micrometer: A new proposal. Cancer 86, 1035–1043 (1999).

    Article  CAS  PubMed  Google Scholar 

  44. van der Aa, M. N. M. et al. A new system for substaging pT1 papillary bladder cancer: a prognostic evaluation. Hum. Pathol. 36, 981–986 (2005).

    Article  CAS  PubMed  Google Scholar 

  45. van Rhijn, B. W. G. et al. A new and highly prognostic system to discern T1 bladder cancer substage. Eur. Urol. 61, 378–384 (2012).

    Article  PubMed  Google Scholar 

  46. Brimo, F. et al. Prognostic factors in T1 bladder urothelial carcinoma: the value of recording millimetric depth of invasion, diameter of invasive carcinoma, and muscularis mucosa invasion. Hum. Pathol. 44, 95–102 (2013).

    Article  PubMed  Google Scholar 

  47. Chang, W.-C., Chang, Y.-H. & Pan, C.-C. Prognostic significance in substaging ofT1 urinary bladder urothelial carcinoma on transurethral resection. Am. J. Surg. Pathol. 36, 454–461 (2012).

    Article  PubMed  Google Scholar 

  48. Brierley, J. D., Gospodarowicz, M. K. & Wittekind, C. TNM Classification of Malignant Tumours (John Wiley & Sons, 2016).

    Google Scholar 

  49. Ananthanarayanan, V. et al. Influence of histologic criteria and confounding factors in staging equivocal cases for microscopic perivesical tissue invasion (pT3a): an interobserver study among genitourinary pathologists. Am. J. Surg. Pathol. 38, 167–175 (2014).

    Article  PubMed  Google Scholar 

  50. Varinot, J. et al. Full analysis of the prostatic urethra at the time of radical cystoprostatectomy for bladder cancer: impact on final disease stage. Virchows Arch. Int. J. Pathol. 455, 449–453 (2009).

    Article  Google Scholar 

  51. Lopez-Beltran, A., Bassi, P., Pavone-Macaluso, M. & Montironi, R. Handling and pathology reporting of specimens with carcinoma of the urinary bladder, ureter, and renal pelvis. Eur. Urol. 45, 257–266 (2004).

    Article  PubMed  Google Scholar 

  52. Prakash et al. Urinary bladder diverticulum and its association with malignancy: an anatomical study on cadavers. Rom. J. Morphol. Embryol. 51, 543–545 (2010).

    CAS  PubMed  Google Scholar 

  53. Walker, N. F., Gan, C., Olsburgh, J. & Khan, M. S. Diagnosis and management of intradiverticular bladder tumours. Nat. Rev. Urol. 11, 383–390 (2014).

    Article  PubMed  Google Scholar 

  54. Golijanin, D., Yossepowitch, O., Beck, S. D., Sogani, P. & Dalbagni, G. Carcinoma in a bladder diverticulum: presentation & treatment outcome. J. Urol. 170, 1761–1764 (2003).

    Article  PubMed  Google Scholar 

  55. Gopalan, A. et al. Urachal carcinoma: a clinicopathologic analysis of 24 cases with outcome correlation. Am. J. Surg. Pathol. 33, 659–668 (2009).

    Article  PubMed  PubMed Central  Google Scholar 

  56. Sheldon, C. A., Clayman, R. V., Gonzalez, R., Williams, R. D. & Fraley, E. E. Malignant urachal lesions. J. Urol. 131, 1–8 (1984).

    Article  CAS  PubMed  Google Scholar 

  57. Bruins, H. M. et al. The impact of the extent of lymphadenectomy on oncologic outcomes in patients undergoing radical cystectomy for bladder cancer: a systematic review. Eur. Urol. 66, 1065–1077 (2014).

    Article  PubMed  Google Scholar 

  58. Lee, D. et al. Lymph node density versus the American Joint Committee on Cancer TNM nodal staging system in node-positive bladder cancer in patients undergoing extended or super-extended pelvic lymphadenectomy. Urol. Oncol. 35, 151.e1–151.e7 (2017).

    Article  Google Scholar 

  59. Zehnder, P. et al. Radical cystectomy with super-extended lymphadenectomy: impact of separate versus en bloc lymph node submission on analysis and outcomes. BJU Int. 117, 253–259 (2016).

    Article  PubMed  Google Scholar 

  60. Stein, J. P., Cai, J., Groshen, S. & Skinner, D. G. Risk factors for patients with pelvic lymph node metastases following radical cystectomy with en bloc pelvic lymphadenectomy: concept of lymph node density. J. Urol. 170, 35–41 (2003).

    Article  PubMed  Google Scholar 

  61. Amin, M. B. et al. The Eighth Edition AJCC Cancer Staging Manual: Continuing to build a bridge from a population-based to a more 'personalized' approach to cancer staging. CA. Cancer J. Clin. 67, 93–99 (2017).

    Article  Google Scholar 

  62. Perry-Keene, J., Ferguson, P., Samaratunga, H., Nacey, J. N. & Delahunt, B. Effective maybe, but is it cost-effective? A reply. Histopathology 65, 729–730 (2014).

    Article  PubMed  Google Scholar 

  63. Perry-Keene, J., Ferguson, P., Samaratunga, H., Nacey, J. N. & Delahunt, B. Total submission of pelvic lymphadenectomy tissues removed during radical prostatectomy for prostate cancer increases lymph node yield and detection of micrometastases. Histopathology 64, 399–404 (2014).

    Article  PubMed  Google Scholar 

  64. Masson-Lecomte, A. et al. External validation of extranodal extension and lymph node density as predictors of survival in node-positive bladder cancer after radical cystectomy. Ann. Surg. Oncol. 20, 1389–1394 (2013).

    Article  PubMed  Google Scholar 

  65. Engvad, B., Poulsen, M. H., Staun, P. W., Walter, S. & Marcussen, N. Histological step sectioning of pelvic lymph nodes increases the number of identified lymph node metastases. Virchows Arch. 464, 45–52 (2014).

    Article  CAS  PubMed  Google Scholar 

  66. Wang, H. J., Solanki, S., Traboulsi, S., Kassouf, W. & Brimo, F. Neoadjuvant chemotherapy-related histologic changes in radical cystectomy: assessment accuracy and prediction of response. Hum. Pathol. 53, 35–40 (2016).

    Article  CAS  PubMed  Google Scholar 

  67. Knowles, M. A. & Hurst, C. D. Molecular biology of bladder cancer: new insights into pathogenesis and clinical diversity. Nat. Rev. Cancer 15, 25–41 (2015).

    Article  CAS  PubMed  Google Scholar 

  68. Majewski, T. et al. Understanding the development of human bladder cancer by using a whole-organ genomic mapping strategy. Lab. Invest. 88, 694–721 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  69. Nguyen, D. P. & Thalmann, G. N. Contemporary update on neoadjuvant therapy for bladder cancer. Nat. Rev. Urol. 14, 348–358 (2017).

    Article  CAS  PubMed  Google Scholar 

  70. Sjödahl, G. et al. A molecular taxonomy for urothelial carcinoma. Clin. Cancer Res. 18, 3377–3386 (2012).

    Article  CAS  PubMed  Google Scholar 

  71. Patschan, O. et al. A molecular pathologic framework for risk stratification of stage T1 urothelial carcinoma. Eur. Urol. 68, 824–836 (2015).

    Article  CAS  PubMed  Google Scholar 

  72. Choi, W. et al. Identification of distinct basal and luminal subtypes of muscle-invasive bladder cancer with different sensitivities to frontline chemotherapy. Cancer Cell 25, 152–165 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  73. Damrauer, J. S. et al. Intrinsic subtypes of high-grade bladder cancer reflect the hallmarks of breast cancer biology. Proc. Natl Acad. Sci. USA 111, 3110–3115 (2014).

    Article  CAS  PubMed  Google Scholar 

  74. Lerner, S. P. et al. Bladder cancer molecular taxonomy: summary from a consensus meeting. Bladder Cancer 2, 37–47 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  75. Rebouissou, S. et al. EGFR as a potential therapeutic target for a subset of muscle-invasive bladder cancers presenting a basal-like phenotype. Sci. Transl. Med. 6, 244ra91 (2014).

    Article  CAS  PubMed  Google Scholar 

  76. Sjödahl, G., Eriksson, P., Liedberg, F. & Höglund, M. Molecular classification of urothelial carcinoma: global mRNA classification versus tumour-cell phenotype classification. J. Pathol. 242, 113–125 (2017).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  77. McConkey, D. J. et al. A prognostic gene expression signature in the molecular classification of chemotherapy-naïve urothelial cancer is predictive of clinical outcomes from neoadjuvant chemotherapy: a phase 2 trial of dose-dense methotrexate, vinblastine, doxorubicin, and cisplatin with bevacizumab in urothelial cancer. Eur. Urol. 69, 855–862 (2016).

    Article  CAS  PubMed  Google Scholar 

  78. Plimack, E. R. et al. Defects in DNA repair genes predict response to neoadjuvant cisplatin-based chemotherapy in muscle-invasive bladder cancer. Eur. Urol. 68, 959–967 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  79. Seiler, R. et al. Impact of molecular subtypes in muscle-invasive bladder cancer on predicting response and survival after neoadjuvant chemotherapy. Eur. Urol. 72, 544–554 (2017).

    Article  CAS  PubMed  Google Scholar 

  80. Powles, T. et al. MPDL3280A (anti-PD-L1) treatment leads to clinical activity in metastatic bladder cancer. Nature 515, 558–562 (2014).

    Article  CAS  PubMed  Google Scholar 

  81. Kardos, J. et al. Claudin-low bladder tumors are immune infiltrated and actively immune suppressed. JCI Insight 1, e85902 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  82. International Collaboration on Cancer Reporting. Urinary Tract Carcinoma Histopathology Reporting Guide Transurethral Resection and Biopsy Specimen. ICCR http://www.iccr-cancer.org/datasets/datasets-under-consultation/datasets-for-comment/iccr-urinary-tract-tur-and-biopsy-bookmarked1st-ed (2018).

  83. International Collaboration on Cancer Reporting. Carcinoma of the Bladder Histopathology Reporting Guide Cystectomy, Cystoprostatectomy and Diverticulectomy Specimen. ICCR http://www.iccr-cancer.org/datasets/datasets-under-consultation/datasets-for-comment/iccr-urinary-tract-bladder-bookmarked1st-edition-v (2018).

  84. Merlin, T., Weston, A. & Tooher, R. Extending an evidence hierarchy to include topics other than treatment: revising the Australian 'levels of evidence'. BMC Med. Res. Methodol. 9, 34 (2009).

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Contributions

E.C. researched data for the article. E.C. and F.B. made substantial contributions to discussion of the article content and wrote the manuscript. All authors reviewed and/or edited the manuscript before submission.

Corresponding author

Correspondence to Eva Compérat.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

PowerPoint slides

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Compérat, E., Varinot, J., Moroch, J. et al. A practical guide to bladder cancer pathology. Nat Rev Urol 15, 143–154 (2018). https://doi.org/10.1038/nrurol.2018.2

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nrurol.2018.2

This article is cited by

Search

Quick links

Nature Briefing: Cancer

Sign up for the Nature Briefing: Cancer newsletter — what matters in cancer research, free to your inbox weekly.

Get what matters in cancer research, free to your inbox weekly. Sign up for Nature Briefing: Cancer