TRPS1 expression in breast angiosarcoma

Angiosarcoma (AS) of the breast, a rare mesenchymal neoplasm, exhibits distinct forms based on etiological and genetic features. While cases with typical clinical presentation and morphology allow for a straightforward diagnosis, challenges arise when clinical data are scarce, diagnostic material is...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Pancsa Tamás
Pósfai Boglárka
Schubert Anna
Almási Szintia
Papp Eszter
ChangChien Yi-Che
Kálmán Endre
Kovács Attila
Kulka Janina
Varga Linda
Cserni Gábor
Kuthi Levente
Dokumentumtípus: Cikk
Megjelent: 2024
Sorozat:VIRCHOWS ARCHIV
Tárgyszavak:
doi:10.1007/s00428-024-03852-2

mtmt:35061763
Online Access:http://publicatio.bibl.u-szeged.hu/33461
Leíró adatok
Tartalmi kivonat:Angiosarcoma (AS) of the breast, a rare mesenchymal neoplasm, exhibits distinct forms based on etiological and genetic features. While cases with typical clinical presentation and morphology allow for a straightforward diagnosis, challenges arise when clinical data are scarce, diagnostic material is limited, or morphological characteristics overlap with other tumors, including undifferentiated carcinomas. The trichorhinophalangeal syndrome protein 1 (TRPS1), once regarded as highly specific for breast carcinomas, now faces doubts regarding its reliability. This study explores TRPS1 expression in breast AS. Our investigation revealed that 60% of AS cases displayed TRPS1 labeling, contrasting with the 40% lacking expression. Scoring by four independent readers established a consensus, designating 12/35 ASs as unequivocally TRPS1-positive. However, uncertainty surrounded nine further cases due to a lack of reader agreement (being substantial as reflected by a kappa value of 0.76). These findings challenge the perceived specificity of TRPS1, shedding light on its presence in a noteworthy proportion of breast ASs. Consequently, the study underscores the importance of a comprehensive approach in evaluating breast ASs and expands the range of entities within the differential diagnosis associated with TRPS1 labeling.
ISSN:0945-6317