Pei-hang Lee

Kaohsiung, KHQ, Taiwan

Last Updated: 09/26/2026

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Found 12 publications

Genitourinary mesenchymal neoplasms with tumor-defining genetic alterations: A clinicopathologic and molecular correlative study of 71 cases.

Genitourinary mesenchymal neoplasms with tumor-defining genetic alterations: A clinicopathologic and molecular correlative study of 71 cases.

Journal: Human pathology

Published: September 11, 2025

In-frame insertions of SOX10 are highly enriched and characterize a distinct transcriptomic profile in gastrointestinal schwannomas.

In-frame insertions of SOX10 are highly enriched and characterize a distinct transcriptomic profile in gastrointestinal schwannomas.

Journal: The Journal of pathology

Published: November 06, 2024

Small intestine angioleiomyoma as a rare cause of perforation: A case report.

Small intestine angioleiomyoma as a rare cause of perforation: A case report.

Journal: World journal of clinical cases

Published: January 08, 2024

Systematic Characterization of the Clinical and Pathological Features of Schwannomas Harboring SH3PXD2A::HTRA1 Fusion.

Systematic Characterization of the Clinical and Pathological Features of Schwannomas Harboring SH3PXD2A::HTRA1 Fusion.

Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc

Published: October 11, 2023

Extraskeletal Myxoid Chondrosarcomas: The Uncommon Clinicopathologic Manifestations and Significance of TAF15::NR4A3 Fusion.

Extraskeletal Myxoid Chondrosarcomas: The Uncommon Clinicopathologic Manifestations and Significance of TAF15::NR4A3 Fusion.

Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc

Published: November 30, 2022

Characterization of Aberrations in DNA Damage Repair Pathways in Gastrointestinal Stromal Tumors: The Clinicopathologic Relevance of γH2AX and 53BP1 in Correlation with Heterozygous Deletions of CHEK2, BRCA2, and RB1.

Characterization of Aberrations in DNA Damage Repair Pathways in Gastrointestinal Stromal Tumors: The Clinicopathologic Relevance of γH2AX and 53BP1 in Correlation with Heterozygous Deletions of CHEK2, BRCA2, and RB1.

Journal: Cancers

Published: February 25, 2022

Molecular Characterization of Dermatofibrosarcoma Protuberans: The Clinicopathologic Significance of Uncommon Fusion Gene Rearrangements and Their Diagnostic Importance in the Exclusively Subcutaneous and Circumscribed Lesions.

Molecular Characterization of Dermatofibrosarcoma Protuberans: The Clinicopathologic Significance of Uncommon Fusion Gene Rearrangements and Their Diagnostic Importance in the Exclusively Subcutaneous and Circumscribed Lesions.

Journal: The American journal of surgical pathology

Published: January 16, 2022

Adult NTRK-rearranged spindle cell neoplasms of the viscera: with an emphasis on rare locations and heterologous elements.

Adult NTRK-rearranged spindle cell neoplasms of the viscera: with an emphasis on rare locations and heterologous elements.

Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc

Published: October 25, 2021

Myoepithelial and oral intracranial myxoid mesenchymal tumor-like neoplasms as diagnostic considerations of the ever-expanding extracranial myxocollagenous tumors harboring FET-CREB fusions.

Myoepithelial and oral intracranial myxoid mesenchymal tumor-like neoplasms as diagnostic considerations of the ever-expanding extracranial myxocollagenous tumors harboring FET-CREB fusions.

Journal: Pathology, research and practice

Published: October 03, 2021

Superficial ALK-rearranged myxoid spindle cell neoplasm with a novel FMR1-ALK fusion gene.

Superficial ALK-rearranged myxoid spindle cell neoplasm with a novel FMR1-ALK fusion gene.

Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc

Published: September 07, 2021

Clinicopathological and molecular characterisation of USP6-rearranged soft tissue neoplasms: the evidence of genetic relatedness indicates an expanding family with variable bone-forming capacity.

Clinicopathological and molecular characterisation of USP6-rearranged soft tissue neoplasms: the evidence of genetic relatedness indicates an expanding family with variable bone-forming capacity.

Journal: Histopathology

Published: July 31, 2020

RHOA G17V mutation in angioimmunoblastic T-cell lymphoma: A potential biomarker for cytological assessment.

RHOA G17V mutation in angioimmunoblastic T-cell lymphoma: A potential biomarker for cytological assessment.

Journal: Experimental and molecular pathology

Published: April 18, 2019

Showing 1-12 of 12

Last Updated: 09/26/2026