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

Evangelia Vetsiou, Vasileios Mpouras, Christina Nikolaidou, Philippos Klonizakis, Evdokia Mandala, Kyriakos Vamvakis, Kyriakos Psarras, Efthymia Vlachaki

Journal: Hemoglobin 2021;44(3):221-223

PMID: 32605400

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.

Address: Diabetes and Endocrine Department, South Warwickshire National Health Service Foundation Trust, Warwick, Warwickshire, UK.; Second Propedeutical Department of Surgery, Hippokration Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.; Department of Pathology, Hippokration Hospital, Thessaloniki, Greece.; Adult Thalassemia Unit, Second Department of Internal Medicine, Hippokration Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.; Fourth Department of Internal Medicine, Hippokration Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.; Public Health and Social Care, Kavala, Greece.

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