Evidence map›Paper›PMID 37062985›Full record

ArticleInternational journal of surgical pathology2024

Clinicopathologic Classification of Renal Cell Carcinoma in Patients ≤40 Years Old From Peru.

Sonia Kamanda, Lourdes Huanca-Amesquita, Esperanza Milla, Pedram Argani, Jonathan I Epstein

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Article in International journal of surgical pathology, 2024. 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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5 · Who and what money

Authors and funding

5 authors.

Sonia KamandaDepartment of Pathology, The Johns Hopkins Medical Institutions, Baltimore, MD, USA.
Lourdes Huanca-AmesquitaDepartment of Pathology, National Institute of Neoplastic Diseases, Lima, Peru.
Esperanza MillaDepartment of Pathology, National Institute of Neoplastic Diseases, Lima, Peru.
Pedram ArganiDepartment of Pathology, The Johns Hopkins Medical Institutions, Baltimore, MD, USA.ORCID 0000-0001-8797-9474
Jonathan I EpsteinDepartment of Pathology, The Johns Hopkins Medical Institutions, Baltimore, MD, USA.ORCID 0000-0003-1839-6472

Funding

Opportunities for Pathology Trainees in Cancer ResearchT32CA193145 · NCI · JOHNS HOPKINS UNIVERSITY · PI ANDERS, ROBERT A., EBERHART, CHARLES G · 2015 to 2025
$2.6M
NCI NIH HHS T32 CA193145
6 · The paper itself

Abstract

introductionThere are scant data on renal cell carcinoma (RCC) from relatively younger patients in South America using contemporary classification.

methodsFifty-nine consecutively treated patients with RCC (≤40 years old) were assessed from the National Institute of Neoplastic Diseases in Peru from 2008 to 2020 (34 males; 25 females), age range of 13 to 40 years.

resultsMost common presenting symptoms were flank pain (n = 40), hematuria (n = 19), and weight loss (n = 12). Associated conditions included 4 patients with proven or presumed tuberous sclerosis and 1 patient with von Hippel Lindau syndrome, all with clear cell RCC. Tumor histopathology was clear cell RCC in 32 of 59 (54%), chromophobe RCC in 6 of 59 (10%), and 5 of 59 (8%) each of papillary RCC and MiT family translocation-associated RCC. Four of 59 (7%) were FH-deficient RCC and 2 of 59 (3%) remained unclassified. The remaining tumors were isolated examples of clear cell papillary renal cell tumor, eosinophilic solid and cystic RCC (ESC RCC), RCC with fibromyomatous stroma, sarcomatoid RCC, and sarcomatoid clear cell RCC. Of the 4 FH-deficient RCCs, none had the classic morphology. The 5 MiT family translocation RCCs had variable morphology. There were 41 tumors without recurrence or metastases, 3 tumors with local recurrence only, 8 tumors with metastases only, and 7 tumors with both local recurrence and metastases.

conclusionsThe current study demonstrates the importance of special studies in accurately classifying RCC in younger individuals. The distribution of RCC subtypes in younger individuals is similar between 2 representative large institutions of the United States and Peru.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsAdolescentAdultFemaleHematuriaHumansMalePeruTranslocation, GeneticYoung Adultfumarate hydratase deficient renal cell carcinomarenal cell carcinomatranslocation associated renal cell carcinoma

Identifiers

PMID37062985
PMCPMC10577151

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