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

Case Report: Submucosal gastroblastoma with a novel PTCH1::GLI2 gene fusion in a 58-year-old man

6 Sept 2022

Abstract excerpt

Gastroblastoma is a rare biphasic tumor of the stomach that generally presents in young patients. MALAT1-GLI1 gene fusion was considered to be the characteristic molecular alteration of this tumor in previous reports. Herein, we described a 58-year-old man with a mass mainly located in the submucosa of the stomach. Microscopic examination showed a biphasic morphology with the same immunohistochemical phenotype as...

Read the complete abstract on PubMed

Topics

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

Share to Cholangiocarcinoma and Gallbladder Cancer Studies
Share to Hedgehog Signaling Pathway Studies
Share to Oral and Maxillofacial Pathology

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 36147912
DOI: 10.3389/fonc.2022.935914

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Case Report: Submucosal gastroblastoma with a novel PTCH1::GLI2 gene fusion in a 58-year-old manPMID 36147912Read ↗

Gastroblastoma with a novel EWSR1‐CTBP1 fusion presenting in adolescenceSemantic proximity Read ↗

Gastroblastoma without GLI1 and EWSR1 gene breaksSemantic proximity Read ↗

A Distinct Malignant Epithelioid Neoplasm With GLI1 Gene Rearrangements, Frequent S100 Protein Expression, and Metastatic Potential: Expanding the Spectrum of Pathologic Entities With ACTB/MALAT1/PTCH1-GLI1 Fusions.Semantic proximity Read ↗

Head and Neck Mesenchymal Neoplasms With GLI1 Gene AlterationsSemantic proximity Read ↗

NF1 mutation and TUBB3 amplification in gastric histiocytic sarcoma: a case report and literature review.Semantic proximity Read ↗

Multidimensional Profiling of GLI1-Altered Mesenchymal Tumors in Soft TissueSemantic proximity Read ↗

Metastatic Malignant Gastric Glomus Tumour: Multidisciplinary Diagnosis & Treatment of a Rare Clinical EntitySemantic proximity Read ↗

Gastric granular cell tumor: A case report and literature reviewSemantic proximity Read ↗

Recurrent <i><scp>MALAT1–GLI1</scp></i> oncogenic fusion and <i><scp>GLI1</scp></i> up‐regulation define a subset of plexiform fibromyxomaSemantic proximity Read ↗

Plexiform Fibromyxoma with MALAT1–GLI1 Fusion with Limited Myxoid Stroma, Aberrant KIT Expression, and Diffuse D2-40 Expression: A Case ReportSemantic proximity Read ↗

A Comprehensive Clinicopathologic and Molecular Reappraisal of GLI1 -altered Mesenchymal Tumors with Pooled Outcome Analysis Showing Poor Survival in GLI1 - amplified Versus GLI1- rearranged Tumors.Semantic proximity Read ↗

[Clinicopathologic features of gastric plexiform fibromyxoma].Semantic proximity Read ↗

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