Novel NOTCH3 alteration expanding the molecular spectrum of pericytic tumours: report of two cases.

doi:10.1111/his.70051

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

Community

Back to search

Article

Novel NOTCH3 alteration expanding the molecular spectrum of pericytic tumours: report of two cases.

Histopathology - 1 Mar 2026

Ungureanu Irena Antonia, Le Quang Megane, Azmani Rihab, Ancelle Marie, Margot Henri, Chotard Guillaume, Le Loarer François, Truffaux Nathalène

Abstract excerpt

INTRODUCTION: Myofibromas are part of the pericytic tumour family, which includes myopericytomas, glomus tumours and angioleiomyomas. While they typically display benign behaviour when arising in the skin and subcutaneous tissues of the head and neck, rare aggressive variants have been reported, particularly those with visceral or intracranial involvement. The most frequently identified molecular alterations in...

Read the complete abstract on PubMed

Topics

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

Share to NOTCH3 gene
Share to PDGFRB gene
Share to Infant, Newborn
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Receptor, Notch3

Source

Open in PubMed Open full text

Identifiers

PMID: 41263773
DOI: 10.1111/his.70051
PMCID: PMC12891926

Genes

NOTCH3
PDGFRB

Provenance

PubMed metadata and Literature Corpus relationships.