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Differential diagnosis of primary mesenchymal neoplasms of the breast

dc.contributor.buuauthorPOLATKAN, SEYİT ALİ VOLKAN
dc.contributor.buuauthorTOLUNAY, ŞAHSİNE
dc.contributor.buuauthorÖZŞEN, MİNE
dc.contributor.buuauthorYALÇINKAYA, ÜLVİYE
dc.contributor.buuauthorGÖKGÖZ, MUSTAFA ŞEHSUVAR
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentPatoloji Ana Bilim Dalı
dc.contributor.departmentGenel Cerrahi Ana Bilim Dalı
dc.contributor.orcid0000-0002-5771-7649
dc.contributor.researcheridAAI-1609-2021
dc.contributor.researcheridAAI-1612-2021
dc.date.accessioned2025-02-07T05:43:46Z
dc.date.available2025-02-07T05:43:46Z
dc.date.issued2024-06-20
dc.description.abstractObjectiveWhile the majority of breast neoplasms originate from epithelial cells, a rare part of them originate from mesenchymal breast tissue.This study aims to present the histomorphological and clinicoradiological features of our series of primary mesenchymal breast tumors and to discuss the features of these tumors in light of the literature.ObjectiveWhile the majority of breast neoplasms originate from epithelial cells, a rare part of them originate from mesenchymal breast tissue.This study aims to present the histomorphological and clinicoradiological features of our series of primary mesenchymal breast tumors and to discuss the features of these tumors in light of the literature.Materials and methodsCases diagnosed as primary mesenchymal breast tumor in breast resection materials evaluated in our center between 2010 and 2023 were included.ResultsOf the 26 tumors included, 57.7% were diagnosed as benign and 42.3% as malignant mesenchymal tumor. Cases diagnosed as benign mesenchymal tumor were hemangioma, lipoma, extra-abdominal fibromatosis, leiomyoma, angiofibroma, lipomatosis, benign fibrous histiocytoma and granular cell tumor.Histopathological study results were compatible with angiosarcoma in 5 (45.4%), undifferentiated sarcoma in 3 (27.3%), myxofibrosarcoma in 2 (18.2%) cases and rhabdomyosarcoma in 1 (9.1%) case.ResultsOf the 26 tumors included, 57.7% were diagnosed as benign and 42.3% as malignant mesenchymal tumor. Cases diagnosed as benign mesenchymal tumor were hemangioma, lipoma, extra-abdominal fibromatosis, leiomyoma, angiofibroma, lipomatosis, benign fibrous histiocytoma and granular cell tumor.Histopathological study results were compatible with angiosarcoma in 5 (45.4%), undifferentiated sarcoma in 3 (27.3%), myxofibrosarcoma in 2 (18.2%) cases and rhabdomyosarcoma in 1 (9.1%) case.ConclusionPrimary breast sarcomas are rarely seen compared to benign mesenchymal tumors and constitute less than 0.1% of all malignant breast tumors. When histomorphological findings suggestive of a mesenchymal tumor are observed in breast specimens, sufficient sampling should be performed to exclude a possible phyllodes tumor, and clinicoradiological findings should be examined to exclude the possibility of a metastasis.
dc.identifier.doi10.1007/s12094-024-03544-y
dc.identifier.issn1699-048X
dc.identifier.scopus2-s2.0-85196400501
dc.identifier.urihttps://doi.org/10.1007/s12094-024-03544-y
dc.identifier.urihttps://hdl.handle.net/11452/50201
dc.identifier.wos001251206700002
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherSpringer Int Publ Ag
dc.relation.journalClinical & Translational Oncology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.subjectAngiosarcoma
dc.subjectRare
dc.subjectSarcoma
dc.subjectLesions
dc.subjectUpdate
dc.subjectBenign
dc.subjectBreast
dc.subjectMalignant
dc.subjectMesenchymal tumor
dc.subjectSarcoma
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectOncology
dc.titleDifferential diagnosis of primary mesenchymal neoplasms of the breast
dc.typeArticle
dc.typeArticle
dc.type.subtypeEarly Access
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Patoloji Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Genel Cerrahi Ana Bilim Dalı
local.indexed.atWOS
local.indexed.atScopus
relation.isAuthorOfPublication736328be-f008-46e1-825a-46199f11dad9
relation.isAuthorOfPublication88cde6d8-7aff-42a7-8102-4847acdacd8b
relation.isAuthorOfPublication7b478372-ad3a-4f0a-a336-3ebde58856eb
relation.isAuthorOfPublication13dc6562-e9fe-42fa-8973-dcd80444844e
relation.isAuthorOfPublication.latestForDiscovery736328be-f008-46e1-825a-46199f11dad9

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