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Pathol Res Pract ; 254: 155143, 2024 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-38301364

RESUMO

Solitary fibrous tumors (SFTs) are known for their heterogeneous morphology, characterized by a variety of cell shapes and different growth patterns. They can also arise in various anatomical locations, most commonly in extremities and deep soft tissues. Despite this diversity in morphology and location, all SFTs share a common molecular signature involving the NAB2::STAT6 gene fusion. Due to their unpredictable clinical behavior, establishing prognostic factors is crucial. This study aims to evaluate an orbital risk stratification system (RSS) proposed by Huang et al. for use in extraorbital SFTs using a database of 97 cases. The Huang model takes into consideration tumor size, mitotic figures, Ki-67 index, and dominant constituent cell (DCC) as key variables. Survival analysis confirmed the model's predictive value, with higher-risk scores being associated with poorer outcomes. However, in contrast to the orbital SFTs studied by Huang et al., our study did not find a correlation between tumor size and recurrence in extraorbital cases. While the Huang model performs slightly better than other RSS, it falls short on achieving statistical significance in distinguishing recurrence risk groups in extraorbital locations. In conclusion, this study validates the Huang RSS for use in extraorbital SFTs and underscores the importance of considering DCC, mitotic count, and Ki-67 together. However, we found that including tumor size in this model did not improve prognostic significance in extraorbital SFTs. Despite the benefits of this additional RSS, vigilant monitoring remains essential, even in cases classified as low-risk due to the inherent unpredictability of SFT clinical outcomes.


Assuntos
Hemangiopericitoma , Neoplasias Orbitárias , Febre Grave com Síndrome de Trombocitopenia , Tumores Fibrosos Solitários , Humanos , Neoplasias Orbitárias/genética , Prognóstico , Antígeno Ki-67 , Proteínas Repressoras/genética , Tumores Fibrosos Solitários/diagnóstico , Tumores Fibrosos Solitários/genética , Fator de Transcrição STAT6/genética , Medição de Risco , Biomarcadores Tumorais/genética
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