Evidence map›Paper›PMID 41954690›Full record

SynthesisInternational urology and nephrology2026

Renal medullary carcinoma: a systematic review of clinical and radiological findings.

William Weston, Cherry Sit, Derfel Ap Dafydd, Christian Kelly-Morland, Aslam Sohaib, Shraddha Adamane, Thubeena Manickavasagar, Lisa Pickering, David Nicol, Samuel J Withey

Abstract readSystematic ReviewReview
In one paragraph

Synthesis in International urology and nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

10 authors.

William WestonDepartment of Radiology, The Royal Marsden NHS Foundation Trust, London, UK.
Cherry SitDepartment of Radiology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Derfel Ap DafyddDepartment of Radiology, The Royal Marsden NHS Foundation Trust, London, UK.
Christian Kelly-MorlandDepartment of Radiology, The Royal Marsden NHS Foundation Trust, London, UK.
Aslam SohaibDepartment of Radiology, The Royal Marsden NHS Foundation Trust, London, UK.
Shraddha AdamaneDepartment of Pathology, The Royal Marsden NHS Foundation Trust, London, UK.
Thubeena ManickavasagarDepartment of Medical Oncology, The Royal Marsden NHS Foundation Trust, London, UK.
Lisa PickeringDepartment of Medical Oncology, The Royal Marsden NHS Foundation Trust, London, UK.
David NicolDepartment of Urology, The Royal Marsden NHS Foundation Trust, London, UK.
Samuel J WitheyDepartment of Radiology, The Royal Marsden NHS Foundation Trust, London, UK. samuel.withey@nhs.net.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsRenal medullary carcinoma (RMC) is a rare subtype of renal cell carcinoma, typically described in young patients with sickle cell trait, which follows an aggressive course. We aimed to perform a systematic review of all published cases of RMC from 1995 to 2024, to summarise the clinico-pathological and radiological features.

methodsA systematic review of all published cases of RMC from 1995 to 2024 was performed. Patient demographics, clinical presentation, radiological features, metastatic profile, management, and overall survival were recorded. Sub-analysis was performed, grouped by sickle cell status.

results219 cases from 103 articles were included, in addition to 5 previously unreported cases from our institution. 88% of patients had sickle cell haemoglobinopathy (SCH) (n = 168/192), with presentation at a younger age in patients with SCH (27.3 ± 13.7 versus 34.1 ± 19.1 years, p = 0.001). RMC was more frequently observed in the right kidney (64.6%, n = 122/189) than the left kidney (35.4%, n = 67/189) (p = < 0.001). Radiologically, the most common features were a central/endophytic location, hypo-enhancement relative to the adjacent cortex, and infiltrative margins. 20.7% (n = 42/203) were stage III at presentation and 70.9% (n = 144/203) of patients were Stage IV. Overall survival at 3 years was 74% for Stage I-II disease, 23% for Stage III disease, and 9% for Stage IV disease.

conclusionsRegardless of sickle cell status, RMC was shown to present at a relatively young age. It was classically seen as an infiltrative, poorly defined, endophytic tumour, centred on the renal medulla. RMC was found to be more commonly advanced at presentation and the overall survival in patients with nodal or distant metastases was poor.

Indexed as

Carcinoma, MedullaryCarcinoma, Renal CellKidney NeoplasmsHumansSickle Cell TraitRenal cell carcinomaRenal medullary carcinomaRenal medullary neoplasmSickle cell haemoglobinopathy

Identifiers

PMID41954690
PMCPMC13506601

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