Please use this identifier to cite or link to this item: https://doi.org/10.1136/jclinpath-2011-200094
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dc.titleIntranuclear inclusions in epithelial cells of benign proliferative breast lesions
dc.contributor.authorHarada, O.
dc.contributor.authorHoe, R.
dc.contributor.authorLin, J.
dc.contributor.authorThike, A.A.
dc.contributor.authorJara-Lazaro, A.R.
dc.contributor.authorPetersson, F.
dc.contributor.authorTan, P.H.
dc.date.accessioned2016-07-08T09:29:27Z
dc.date.available2016-07-08T09:29:27Z
dc.date.issued2011-09
dc.identifier.citationHarada, O., Hoe, R., Lin, J., Thike, A.A., Jara-Lazaro, A.R., Petersson, F., Tan, P.H. (2011-09). Intranuclear inclusions in epithelial cells of benign proliferative breast lesions. Journal of Clinical Pathology 64 (9) : 776-780. ScholarBank@NUS Repository. https://doi.org/10.1136/jclinpath-2011-200094
dc.identifier.issn00219746
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/125627
dc.description.abstractAim: To document and clarify the nature of intranuclear inclusions of luminal epithelium in benign proliferative breast lesions. Methods and results: Five benign breast lesions were selected which showed intranuclear inclusions within epithelial cells on light microscopy. Following confirmation of their luminal epithelial (non-myoepithelial) localisation by immunohistochemistry, ultrastructural examination was performed with the following observations: (1) presence of deep nuclear indentations occasionally verging on nuclear inclusions; (2) inclusions with features of helioid bodies; and (3) a morphological spectrum of helioid bodies and their focal coexistence. Conclusion: Intranuclear inclusions of breast epithelium are likely of cytoplasmic origin. Helioid bodies may be formed by a stepwise process, the nature of which needs further study.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1136/jclinpath-2011-200094
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentPATHOLOGY
dc.description.doi10.1136/jclinpath-2011-200094
dc.description.sourcetitleJournal of Clinical Pathology
dc.description.volume64
dc.description.issue9
dc.description.page776-780
dc.description.codenJCPAA
dc.identifier.isiut000294013500008
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