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Necrobiosis Lipoidica in a Patient with β-Thalassemia Major: A Case Report and Review of the Literature.

TitleNecrobiosis Lipoidica in a Patient with β-Thalassemia Major: A Case Report and Review of the Literature.
Publication TypeJournal Article
Year of Publication2020
AuthorsVetsiou, E., Mpouras V., Nikolaidou C., Klonizakis P., Mandala E., Vamvakis K., Psarras K., & Vlachaki E.
JournalHemoglobin
Volume44
Issue3
Pagination221-223
Date Published2020 May
ISSN1532-432X
Abstract

Necrobiosis lipoidica (NL) is a rare granulomatous disease that predominantly affects middle-aged women and is often associated with diabetes mellitus (DM), rheumatoid arthritis (RA) and other metabolic disorders. Thalassemias are the most common hereditary hemoglobin (Hb) disorders worldwide. A few studies investigated dermatologic problems that coexist with β-thalassemia major (β-TM). The most common skin disorders in patients with β-TM are xerosis, urticaria, pseudoxanthoma, hyperpigmentation, leg ulcers and small-vessel vasculitis. Necrobiosis lipoidica has only been occasionally reported in patients with β-TM. Herein, we present a female with β-TM and NL. Furthermore, a brief review of the literature was performed.

DOI10.1080/03630269.2020.1783287
Alternate JournalHemoglobin
PubMed ID32605400

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