Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/119035
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dc.creatorBartosch, C
dc.creatorMendes, N
dc.creatorRios, E
dc.creatorRodrigues, M
dc.creatorEloy, C
dc.creatorReis, CA
dc.creatorAmendoeira, I
dc.date.accessioned2019-02-21T12:16:17Z-
dc.date.available2019-02-21T12:16:17Z-
dc.date.issued2015
dc.identifier.issn0344-0338
dc.identifier.urihttps://hdl.handle.net/10216/119035-
dc.description.abstractSignet-ring cells are relatively common in breast cancers but are frequently overlooked. Although previously defined as a subtype of mucin producing carcinomas, breast carcinomas with signet-ring cell (SRC) differentiation nowadays are not considered a distinct entity.The objective of the present study was to characterize the morphological features and mucin expression profile of breast carcinomas with SRC differentiation. All breast carcinomas diagnosed at Centro Hospitalar S. Joao between 1996 and 2006 in which the pathology report mentioned the presence of SRCs (n= 11) and four mucinous carcinomas were included in the study. The frequency of SRCs and immunohistochemistry expression of MUC1/MUC2/MUC5AC/MUC6 were evaluated.We confirmed that SRC differentiation can occur in different histological types, including ductal, lobular, mucinous and metaplastic carcinomas. The proportion of SRCs was highly variable (range: 8-70%). Tumors encompassed SRCs of intracytoplasmic lumina and goblet-cell type. A higher percentage of SRCs was associated with lymphovascular invasion (p= 0.047). All tumors expressed cytoplasmic and membranous MUC1. Secretory mucins were more frequent in mucinous carcinomas and in carcinomas with extensive SRC differentiation.We conclude that besides the usefulness of mucin immunodetection for the differential diagnosis of carcinomas with SRC differentiation of breast origin, it is important to report SRC differentiation regardless of histological type because of its intrinsic prognostic value.
dc.description.sponsorshipWe especially thank Professor Sobrinho-Simões for the careful review of the manuscript. IPATIMUP integrates the i3S Research Unit, which is partially supported by FCT, the Portuguese Foundation for Science and Technology. This work is funded by FEDER funds through the Operational Program for Competitiveness Factors-COMPETE and National Funds through the FCT-Foundation for Science and Technology , under the projects: PEst-C/SAU/LA0003/2013 and PTDC/BBB-EBI/0786/2012 .
dc.language.isoeng
dc.publisherElsevier
dc.relationinfo:eu-repo/grantAgreement/FCT/COMPETE/132983/PT
dc.relationinfo:eu-repo/grantAgreement/FCT/COMPETE/125428/PT
dc.relation.ispartofPathology Research and Practice, vol.211(8), p. 588-595
dc.rightsopenAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectAdult
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectBiomarkers, Tumor/metabolism
dc.subjectBreast Neoplasms/metabolism
dc.subjectBreast Neoplasms/pathology
dc.subjectCarcinoma, Signet Ring Cell/metabolism
dc.subjectCell Differentiation/physiology
dc.subjectCell Shape
dc.subjectFemale
dc.subjectHumans
dc.subjectImmunohistochemistry/methods
dc.subjectMembrane Glycoproteins/metabolism
dc.subjectMiddle Aged
dc.subjectMucins/metabolism
dc.subjectStomach Neoplasms/metabolism
dc.subjectStomach Neoplasms/pathology
dc.titleMorphological features and mucin expression profile of breast carcinomas with signet-ring cell differentiation
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.1016/j.prp.2015.05.003
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0344033815000977?via%3Dihub
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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