Composite eosinophilic solid and cystic renal cell carcinoma and clear cell renal cell carcinoma: a rare case report and literature review.
Clear cell renal cell carcinoma
Eosinophilic solid and cystic renal cell carcinoma
Renal composite tumors
Surgery
Journal
BMC urology
ISSN: 1471-2490
Titre abrégé: BMC Urol
Pays: England
ID NLM: 100968571
Informations de publication
Date de publication:
30 Jul 2024
30 Jul 2024
Historique:
received:
08
05
2024
accepted:
11
07
2024
medline:
31
7
2024
pubmed:
31
7
2024
entrez:
30
7
2024
Statut:
epublish
Résumé
Eosinophilic solid and cystic renal cell carcinoma (ESC-RCC) is a novel subtype of renal cell carcinoma characterized by its relatively low incidence and indolent behavior. We report a rare case of ESC-RCC concurrent with clear cell renal cell carcinoma (ccRCC) in a single kidney. A 48-year-old male, was found to have a mixed echogenic mass in the left kidney during a physical examination. He has no history of hematuria and flank pain. An abdominal CT scan revealed a 3.0 * 1.9 * 2.5 cm We reported a case of renal composite tumors, comprising the rare ESC-RCC and the more common ccRCC. Imaging combined with postoperative pathological examination is crucial for the definitive diagnosis of these rare tumors.
Sections du résumé
BACKGROUND
BACKGROUND
Eosinophilic solid and cystic renal cell carcinoma (ESC-RCC) is a novel subtype of renal cell carcinoma characterized by its relatively low incidence and indolent behavior. We report a rare case of ESC-RCC concurrent with clear cell renal cell carcinoma (ccRCC) in a single kidney.
CASE PRESENTATION
METHODS
A 48-year-old male, was found to have a mixed echogenic mass in the left kidney during a physical examination. He has no history of hematuria and flank pain. An abdominal CT scan revealed a 3.0 * 1.9 * 2.5 cm
CONCLUSION
CONCLUSIONS
We reported a case of renal composite tumors, comprising the rare ESC-RCC and the more common ccRCC. Imaging combined with postoperative pathological examination is crucial for the definitive diagnosis of these rare tumors.
Identifiants
pubmed: 39080639
doi: 10.1186/s12894-024-01542-4
pii: 10.1186/s12894-024-01542-4
doi:
Types de publication
Case Reports
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
160Subventions
Organisme : Innovative Research Program of Xiangyang No.1 People's Hospital
ID : XYY2023SD06 and XYY2023QB07
Organisme : Innovative Research Program of Xiangyang No.1 People's Hospital
ID : XYY2023SD06 and XYY2023QB07
Informations de copyright
© 2024. The Author(s).
Références
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