Evidence map›Paper›PMID 40098178›Full record

ArticleJournal of medical case reports2025

Liver metastasis from a chromophobe renal cell carcinoma 18 years after initial diagnosis: a case report.

Alexandra Ökrösi, Lothar Ponhold, Simon Turba, Melitta Kitzwögerer, Gertraud Heinz

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Article in Journal of medical case reports, 2025. 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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Alexandra ÖkrösiDepartment of Diagnostic and Interventional Radiology, University Hospital of St. Pölten, Dunant-Platz 1, 3100, Sankt Pölten, Austria.
Lothar PonholdDepartment of Diagnostic and Interventional Radiology, University Hospital of St. Pölten, Dunant-Platz 1, 3100, Sankt Pölten, Austria.
Simon TurbaDepartment of Urology and Andrology, University Hospital of St, Pölten, Austria.
Melitta KitzwögererDepartment of Clinical Pathology and Molecular Pathology, University Hospital of St, Pölten, Austria.
Gertraud HeinzDepartment of Diagnostic and Interventional Radiology, University Hospital of St. Pölten, Dunant-Platz 1, 3100, Sankt Pölten, Austria. gertraud.heinz@stpoelten.lknoe.at.ORCID http://orcid.org/0000-0002-6037-7534

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChromophobe renal cell carcinoma is a rare histological subtype, accounting for only 5-6% of renal cell carcinoma cases. It exhibits low aggressiveness and has an overall favorable prognosis with a very low risk of developing metastatic disease. Genetic syndromes such as Birt-Hogg-Dubbé may be associated with this renal cell carcinoma subtype. Owing to limited clinical data, therapeutic regimens for advanced chromophobe renal cell carcinoma are often extrapolated from treatment protocols for clear cell renal cell carcinoma or studies combining several non-clear cell renal cell carcinoma types. CASE PRESENTATION: We report a case of a 54-year-old Austrian male patient presenting with metastatic liver disease from chromophobe renal cell carcinoma, confirmed by biopsy, 18 years after the initial diagnosis of a non-metastasized, grade 2, pNO, pT2 tumor with R0 resection. The patient underwent regular follow-up examinations and had no clinical symptoms at the time of recurrent disease diagnosis. Family history for genetic syndromes was negative. The multidisciplinary tumor board decided to treat the patient with a novel first-line palliative therapy using combined immuno-/tyrosine kinase therapy with pembrolizumab/lenvatinib. A multiphasic computed tomography scan performed 3 months after initiation of therapy showed a complete response.

conclusionAlthough chromophobe renal cell carcinoma typically has excellent progression-free survival and overall survival rates in localized disease, those patients with larger tumors or those with sarcomatous features, as well as PT53 mutations, seem to have worse outcomes due to metastatic development. This case report affirms that patients with chromophobe renal cell carcinoma exhibiting these risk factors should undergo closer and long-term follow-up after curative surgery.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsLiver NeoplasmsAntibodies, Monoclonal, HumanizedHumansMaleMiddle AgedTomography, X-Ray ComputedAntibodies, Monoclonal, HumanizedpembrolizumabCarcinomaCase reportsChromophobe renal cell carcinomaImmunotherapyMolecular targeted therapyNeoplasm metastasisRare diseasesRenal cell

Identifiers

PMID40098178
PMCPMC11912719

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