Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Clear cell and papillary renal cell carcinomas in hereditary papillary renal cell carcinoma (HPRCC) syndrome: a case report.

Diagnostic pathology - 20 Nov 2021

Ferlicot Sophie, Just Pierre-Alexandre, Compérat Eva, Rouleau Etienne, Tissier Frédérique, Vaessen Christophe, Richard Stéphane

Abstract excerpt

BACKGROUND: Hereditary papillary renal cell carcinoma (HPRCC) is a rare autosomal dominant disease characterized by the development of multiple and bilateral papillary type I renal cell carcinomas (RCC) and papillary adenomas caused by activating mutations in the MET proto-oncogene. Classically, distinctive histological features of RCC are described according to the familial renal cell carcinoma syndrome. To...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Carcinoma, Renal Cell
Share to Germ-Line Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Immunohistochemistry

Share to In Situ Hybridization, Fluorescence

Share to Kidney Neoplasms

Share to Neoplastic Syndromes, Hereditary

Share to Proto-Oncogene Proteins c-met

Share to Von Hippel-Lindau Tumor Suppressor Protein

Source

Open in PubMed Open full text

Identifiers

PMID: 34801057
DOI: 10.1186/s13000-021-01170-8
PMCID: PMC8606058

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clear cell and papillary renal cell carcinomas in hereditary papillary renal cell carcinoma (HPRCC) syndrome: a case report.PMID 34801057Read ↗

Various Histological Types of Renal Cell Carcinoma Associated With Hereditary Papillary Renal Cell Carcinoma (HPRCC): a Case ReportSemantic proximity Read ↗

Papillary renal cell carcinoma: A review of the current therapeutic landscape.Semantic proximity Read ↗

Hereditary papillary renal cell carcinomaSemantic proximity Read ↗

Inherited forms of renal cell carcinoma.Semantic proximity Read ↗

Renal cancer in von Hippel-Lindau disease and related syndromes.Semantic proximity Read ↗

Dismantling papillary renal cell carcinoma classification: The heterogeneity of genetic profiles suggests several independent diseasesSemantic proximity Read ↗

Hereditary renal cell carcinoma syndromes: diagnosis, surveillance and managementSemantic proximity Read ↗

Clear cell renal cell carcinoma with wild‐type von Hippel‐Lindau gene: a non‐existent or new tumour entity?Semantic proximity Read ↗

Double Hit in Clear-Cell Renal Cell Carcinoma With Germline Pathogenic ATM Mutation and Somatic VHL Mutation.Semantic proximity Read ↗

Familial clear cell renal cell carcinoma (FCRC): clinical features and mutation analysis of the VHL,MET, and CUL2candidate genesSemantic proximity Read ↗

Hereditary Renal Cell Carcinoma: An Imaging Update.Semantic proximity Read ↗

Novel germline MET pathogenic variants in French patients with papillary renal cell carcinomas type I.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.