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dc.contributor.authorKarabudak O.
dc.contributor.authorTaskapan O.
dc.contributor.authorBozdogan O.
dc.contributor.authorDogan B.
dc.date.accessioned2020-06-25T15:14:06Z
dc.date.available2020-06-25T15:14:06Z
dc.date.issued2008
dc.identifier.issn00195154
dc.identifier.urihttps://doi.org/10.4103/0019-5154.43206
dc.identifier.urihttps://hdl.handle.net/20.500.12587/2028
dc.description.abstractWe describe a 76-year-old man presenting with a chronic, non-healing ulcer of six-year duration on his left zygomatic area. The skin biopsy specimen taken from the lesion, showed increased vascular proliferation, edematous endothelial cells in the dermal blood vessels and perivascular eosinophilic/lymphocytic infiltration. The routine and specific blood tests were unremarkable. On the basis of these features, the patient was diagnosed as having angiolymphoid hyperplasia with eosinophilia (ALHE). We present the case because of its rarity in older people, atypical clinical appearance; and stress the consideration of ALHE in the differential diagnosis of chronic non-healing superficial ulcers confined to face and neck.en_US
dc.language.isoengen_US
dc.publisherMedknow Publications and Media Pvt. Ltden_US
dc.relation.isversionof10.4103/0019-5154.43206en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAngiolymphoid hyperplasia with eosinophiliaen_US
dc.subjectNon-healing ulceren_US
dc.titleAngiolymphoid hyperplasia with eosinophilia: Atypical appeareance in an older patienten_US
dc.typearticleen_US
dc.contributor.departmentKırıkkale Üniversitesien_US
dc.identifier.volume53en_US
dc.identifier.issue3en_US
dc.identifier.startpage144en_US
dc.identifier.endpage145en_US
dc.relation.journalIndian Journal of Dermatologyen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US


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