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

CTNNB1 mutation-driven hybrid tumor: desmoid fibromatosis with an unusual associated epithelioid component arising in association with a neuromuscular choristoma.

Virchows Archiv : an international journal of pathology - 1 Apr 2024

Zheng Xuanxuan, He Xin, Lu Yang, Chen Chang, Zhang Hongying

Abstract excerpt

CTNNB1 mutations play important roles in the development of soft tissue tumors, such as desmoid fibromatosis (DF), sinonasal tract angiofibroma, sinonasal glomangiopericytoma, intranodal palisaded myofibroblastoma, neuromuscular choristoma (NMC), and the recently reported pseudoendocrine sarcoma. Here, we report a unique hybrid soft tissue tumor with classic DF, unusual epithelioid component, and NMC in a...

Read the complete abstract on PubMed

Topics

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

Share to beta Catenin
Share to Biomarkers, Tumor

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Choristoma

Share to Desmoid Tumors

Share to DNA Mutational Analysis

Share to Immunohistochemistry

Share to Mutation, Missense

Share to Soft Tissue Neoplasms

Source

Identifiers

PMID: 38183458
DOI: 10.1007/s00428-023-03729-w

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

CTNNB1 mutation-driven hybrid tumor: desmoid fibromatosis with an unusual associated epithelioid component arising in association with a neuromuscular choristoma.PMID 38183458Read ↗

Frequent CTNNB1 p.S45 Mutations and Aggressive Clinical Behavior in Neuromuscular Choristoma-Associated Fibromatosis.Semantic proximity Read ↗

[Clinicopathological and molecular genetic features of neuromuscular choristoma-associated desmoid type fibromatosis].Semantic proximity Read ↗

Resection of a desmoid-type fibromatosis with a CTNNB1 p.S45P mutation using a cervico-thoracic approach: A case report and literature review.Semantic proximity Read ↗

Pseudoendocrine Sarcoma: Clinicopathologic Analysis of 23 Cases of a Distinctive Soft Tissue Neoplasm With Metastatic Potential, Recurrent CTNNB1 Mutations, and a Predilection for Truncal Locations.Semantic proximity Read ↗

Clinicopathological features of 70 desmoid-type fibromatoses confirmed by β-catenin immunohistochemical staining and CTNNB1 mutation analysis.Semantic proximity Read ↗

CD34-Positive Spindle Cell Tumor With CTNNB1 Mutation: An Unusual Spindle Cell Variant of Sinonasal Glomangiopericytoma.Semantic proximity Read ↗

Adipocyte-rich CTNNB1-mutated Intramuscular Gardner Fibroma Progressing to Desmoid Fibromatosis.Semantic proximity Read ↗

CTNNB1 and APC Mutations in Sinonasal Myxoma : Expanding the Spectrum of Tumors Driven By WNT/β-catenin Pathway.Semantic proximity Read ↗

Superficial fibromas with CTNNB1 mutation.Semantic proximity Read ↗

Desmoplastic fibroma of the pediatric cranium with CTNNB1 mutation: case report and literature review.Semantic proximity Read ↗

Clinicopathologic Diversity of Undifferentiated Sarcoma With BCOR-CCNB3 Fusion: Analysis of 11 Cases With a Reappraisal of the Utility of Immunohistochemistry for BCOR and CCNB3.Semantic proximity Read ↗

Novel pathogenic alterations in pediatric and adult desmoid-type fibromatosis – A systematic analysis of 204 casesSemantic proximity Read ↗

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