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dc.contributor.authorKoçak M.
dc.contributor.authorKeleş H.
dc.contributor.authorYakaryilmaz F.
dc.contributor.authorBozdoğan Ö.
dc.contributor.authorGüliter S.
dc.date.accessioned2020-06-25T15:14:17Z
dc.date.available2020-06-25T15:14:17Z
dc.date.issued2009
dc.identifier.issn00195154
dc.identifier.urihttps://doi.org/10.4103/0019-5154.57616
dc.identifier.urihttps://hdl.handle.net/20.500.12587/2067
dc.description.abstractDiffuse plane xanthomas are characterized by the presence of yellowish plaques on the eyelids, neck, upper trunk, buttocks, and flexural folds. Histology shows foamy histiocytes in the dermis. Approximately half of the cases are associated with lymphoproliferative disorders. Budd-Chiari syndrome is an uncommon condition induced by thrombotic or nonthrombotic obstruction of hepatic venous outflow. We present a case of diffuse plane xanthoma in a 62-year-old man who developed normolipemic plane xanthomas coinciding with Budd-Chiari syndrome and monoclonal gammopathy. We review the English-language literature regarding the rare association of xanthomas and Budd-Chiari syndrome.en_US
dc.language.isoengen_US
dc.relation.isversionof10.4103/0019-5154.57616en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBudd-Chiari syndromeen_US
dc.subjectDiffuse plane xanthomaen_US
dc.subjectMonoclonal gammopathyen_US
dc.titleDiffuse plane xanthomatosis in a patient with Budd-Chiari syndrome and monoclonal gammopathyen_US
dc.typearticleen_US
dc.contributor.departmentKırıkkale Üniversitesien_US
dc.identifier.volume54en_US
dc.identifier.issue4en_US
dc.identifier.startpage369en_US
dc.identifier.endpage371en_US
dc.relation.journalIndian Journal of Dermatologyen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US


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