Please use this identifier to cite or link to this item: https://hdl.handle.net/1/1067
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dc.contributor.authorWylie, Brenton-
dc.contributor.otherDickison, P.-
dc.contributor.otherHoward, V.-
dc.contributor.otherSmith, Saxon D-
dc.date.accessioned2018-02-07T00:37:02Zen
dc.date.available2018-02-07T00:37:02Zen
dc.date.issued2016-10-
dc.identifier.citation41(7):764-7en
dc.identifier.issn0307-6938en
dc.identifier.urihttps://elibrary.cclhd.health.nsw.gov.au/cclhdjspui/handle/1/1067en
dc.description.abstractSystemic AL amyloidosis is known to be associated with plasma cell dyscrasias, including multiple myeloma. The cutaneous manifestations of systemic AL amyloidosis are varied, but typically include waxy plaques or subcutaneous nodules. We report a woman who presented with bilateral eruptions of hyperpigmented plaques in her axillae, which were diagnosed as milia en plaque. She had a history of multiple myeloma, for which she was under the care of a haematologist. This is the first documented case, to our knowledge, of an eruption in the axillae being milia en plaque.en
dc.description.sponsorshipHaematologyen
dc.description.sponsorshipDermatologyen
dc.titleLocalized axillary milia en plaque: a rare cutaneous case presentation of systemic amyloidosisen
dc.typeJournal Articleen
dc.identifier.doi10.1111/ced.12914en
dc.description.pubmedurihttps://www.ncbi.nlm.nih.gov/pubmed/27663153en
dc.description.affiliatesCentral Coast Local Health Districten
dc.description.affiliatesGosford Hospitalen
dc.identifier.journaltitleClinical and experimental dermatologyen
dc.type.studyortrialCase Series and Case Reportsen
dc.originaltypeTexten
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
Appears in Collections:Oncology / Cancer
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