Necrobiosis lipoidica in a patient with β-thalassemia major: a case report and review of the literature
Author
Vetsiou, EvangeliaMpouras, Vasileios
Nikolaidou, Christina
Klonizakis, Philippos
Mandala, Evdokia
Vamvakis, Kyriakos
Psarras, Kyriakos
Vlachaki, Efthymia
Affiliation
South Warwickshire University NHS Foundation Trust; Hippokration Hospital, Aristotle University of Thessaloniki, Greece; Public Health and Social Care, Kavala, GreecePublication date
2020-07Subject
Endocrinology
Metadata
Show full item recordAbstract
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. Keywords: ferritin; necrobiosis lipoidica (NL); reactive oxygen species (ROS); β-Thalassemia major (β-TM).Citation
Vetsiou E, Mpouras V, Nikolaidou C, Klonizakis P, Mandala E, Vamvakis K, Psarras K, Vlachaki E. Necrobiosis Lipoidica in a Patient with β-Thalassemia Major: A Case Report and Review of the Literature. Hemoglobin. 2020 May;44(3):221-223. doi: 10.1080/03630269.2020.1783287. Epub 2020 Jul 1.Type
ArticlePMID
32605400Journal
HemoglobinPublisher
Taylor and Francis Groupae974a485f413a2113503eed53cd6c53
10.1080/03630269.2020.1783287