Key result
A panel comprising loss of YAP1 C-terminus expression, TFE3 positivity, and CAMTA1 negativity serves as sensitive markers for detecting lung EHE with YAP1::TFE3 fusion.
Why the study?
YAP1::TFE3 fused epithelioid hemangioendothelioma presents a diagnostic challenge in routine practice due to its rarity and morphologic overlap with other epithelioid tumors.
Case Report (n=1)
Identifies a specific immunohistochemical panel to aid in the challenging diagnosis of a rare subtype of lung epithelioid hemangioendothelioma.
Epithelioid hemangioendothelioma (EHE) is a rare and low-grade malignant endothelial sarcoma. Based on disease-defining mutations, approximately 95% of EHEs have the conventional WWTR1::CAMTA1 gene fusion, while approximately 5% are the Yes-associated protein-1 (YAP1):: transcription factor binding to IGHM enhancer 3 (TFE3) fused tumor subtype according to the World Health Organization classification. Although this tumor type is well recognized, EHE, especially the YAP1 :: TFE3 fused tumor subtype, represents a diagnostic challenge in routine practice due to its rarity and morphologic overlap with other epithelioid tumors, including other benign and malignant epithelioid vascular neoplasms or carcinomas. Here, we highlight the loss of YAP1 C-terminus expression from the nucleus and cytoplasm of tumor cells along with TFE3 positivity and CAMTA1 negativity as a panel of sensitive markers for detecting lung EHE with YAP1 :: TFE3 fusion. We also briefly describe the clinicopathological characteristics of this tumor subtype and detail its relevant differential diagnosis.
No takes yet. Share an insight, caveat, or question.
Xiao et al. (2025) conducted a case report in Lung Epithelioid Hemangioendothelioma with YAP1::TFE3 Fusion (n=1). Diagnostic marker panel (YAP1 C-terminus loss, TFE3 positivity, CAMTA1 negativity) was evaluated. A panel comprising loss of YAP1 C-terminus expression, TFE3 positivity, and CAMTA1 negativity serves as sensitive markers for detecting lung EHE with YAP1::TFE3 fusion.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: