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.

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.

Keywords: ferritin; necrobiosis lipoidica (NL); reactive oxygen species (ROS); β-Thalassemia major (β-TM).

Publication types

  • Case Reports
  • Review

MeSH terms

  • Biopsy
  • Disease Management
  • Disease Susceptibility
  • Female
  • Humans
  • Immunohistochemistry
  • Iron Overload / diagnosis
  • Iron Overload / drug therapy
  • Iron Overload / etiology
  • Iron Overload / metabolism
  • Middle Aged
  • Necrobiosis Lipoidica / complications*
  • Necrobiosis Lipoidica / diagnosis*
  • Skin / pathology
  • beta-Thalassemia / complications*
  • beta-Thalassemia / diagnosis
  • beta-Thalassemia / therapy