Bellini’s collecting duct renal carcinoma: report of two cases and review of the literature

Authors

  • Garazi Gutiérrez-Zurimendi Hospital Universitario Cruces, Barakaldo, Bizkaia. España
  • Gonzalo García de Casasola-Rodríguez Hospital Universitario Cruces, Barakaldo, Bizkaia. España
  • Ibon Urrestizala-Peña Hospital Universitario Galdakao, Galdakao, Bizkaia. España
  • Mikel Aizcorbe-Gómez Hospital Universitario Cruces, Barakaldo, Bizkaia. España
  • Asier Maldonado-De Sasia Hospital Universitario Cruces, Barakaldo, Bizkaia. España
  • Aranzazu Urresola-Olabarrieta Hospital Universitario Cruces, Barakaldo, Bizkaia. España

DOI:

https://doi.org/10.48193/revistamexicanadeurologa.v82i1.730

Keywords:

Bellini’s collecting duct renal carcinoma, renal cancer, urothelial cancer, nephrectomy, chemotherapy

Abstract

Abstract

Clinical cases: We present two cases of Bellini’s Collecting Duct Renal Carcinoma (CDRC) that appear as suspicious kidney masses with enhancement of the urotelium, without a determinant radiological appearance, diagnosed by anatomo-pathological analysis. We revise the medical history, histological findings and make a review of the literature.

Importance / Clinical implication: Bellini’s collecting duct renal carcinoma is a very rare and aggressive type of kidney cancer (less than 1%), usually diagnosed at advanced stages. It does not present specific radiological characteristics, which makes necessary the histologic and inmunohistochemical analysis to confirm the diagnosis. We must suspect CDRC in infiltrative medular renal masses that do not affect kidney shape, and treat as soon as possible performing surgery, whenever feasible, normally associated with adjuvant chemotherapy. Nevertheless, it usually has an unfavourable evolution.

Conclusion: It is imperative to diagnose and treat this kind of tumours as soon as possible due to its aggressiveness and fatal prognosis.

 

References

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Published

2022-02-21 — Updated on 2022-02-22

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Clinical cases