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Acquired ichthyosis triggered by an osseous hemangiopericytoma: a case report and review of the literature.

TitleAcquired ichthyosis triggered by an osseous hemangiopericytoma: a case report and review of the literature.
Publication TypeJournal Article
Year of Publication2014
AuthorsPatsatsi, A., Kyriakou A., Karavasilis V., Tsatsou F., Lazaridis G., Kalabalikis D., & Sotiriadis D.
JournalCase Rep Dermatol
Volume6
Issue1
Pagination10-5
Date Published2014 Jan
ISSN1662-6567
Abstract

Ichthyoses are a heterogeneous group of cutaneous keratinization disorders that can be congenital or acquired. Apart from neoplastic disorders, the acquired form of ichthyosis (AI) has been associated with a variety of diseases including infections, autoimmune/inflammatory and endocrine/metabolic diseases as well as nutritional conditions, medications and others. However, malignancy accounts for half of the reported cases, most commonly including lymphoproliferative disorders. We present a case of AI as a paraneoplastic skin manifestation of a primary, osseous hemangiopericytoma (HP) accompanied by multiple liver metastases. We also review the literature and discuss the necessity of investigating underlying diseases, especially malignancy, when adult-onset ichthyosis arises.

DOI10.1159/000358294
Alternate JournalCase Rep Dermatol
PubMed ID24575005
PubMed Central IDPMC3934780

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