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dc.contributor.author김정수-
dc.date.accessioned2018-03-12T08:58:27Z-
dc.date.available2018-03-12T08:58:27Z-
dc.date.issued2013-08-
dc.identifier.citationClinical and Experimental Dermatology, Aug 2013, 38(6), P.617-621en_US
dc.identifier.issn0307-6938-
dc.identifier.urihttp://onlinelibrary.wiley.com/doi/10.1111/ced.12088/abstract-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/45607-
dc.description.abstractEccrine angiomatous hamartoma (EAH) is a benign hamartomatous tumour characterized by a combination of proliferative eccrine and vascular elements. Papillary haemangioma (PH) is a distinct cutaneous haemangioma with predominantly intravascular capillary proliferation within dilated thin-walled blood vessels. EAHs have been reported in combination with various vascular components. We present the first case in the dermatological literature, to our knowledge, of a patient with congenital EAH with the histopathological features of a PH.en_US
dc.language.isoenen_US
dc.publisherWiley-Blackwellen_US
dc.subjectGLOMERULOID HEMANGIOMAen_US
dc.subjectPOEMS SYNDROMEen_US
dc.subjectVARIANTen_US
dc.titleAn eccrine angiomatous hamartoma with histopathological features of a papillary haemangioma in a neonateen_US
dc.typeArticleen_US
dc.relation.volume38-
dc.identifier.doi10.1111/ced.12088-
dc.relation.page617-621-
dc.relation.journalCLINICAL AND EXPERIMENTAL DERMATOLOGY-
dc.contributor.googleauthorPaek, J.-O.-
dc.contributor.googleauthorKang, H.-S.-
dc.contributor.googleauthorLee, M.-W.-
dc.contributor.googleauthorKim, J.-S.-
dc.relation.code2013009442-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidtuentuen-
dc.identifier.researcherID35102450900-
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COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
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