| Literature DB >> 31522454 |
Marzieh Maddah1, Mohammad Reza Fazlollahi2, Reza Shiari3, Farhad Shahram4, Setareh Mamishi5, Delara Babaie6, Maryam Monajemzadeh7, Soheila Sotudeh8, Amir Ali Hamidieh9, Mohsen Badalzadeh10, Shaghayegh Tajik11, Leila Sedighipour12, Zahra Pourpak13.
Abstract
Chronic granulomatous disease (CGD) is a rare genetic disorder of neutrophil activity, resulting in increased rate of recurrent infections with catalase-positive bacteria and fungi, as well as various autoimmune diseases such as sarcoidosis, rheumatoid arthritis, and discoid and/or systemic lupus erythematosus. Few reports have reported lupus erythematosus (LE) in patients with X-linked CGD (XL-CGD) and carriers, and very few in autosomal recessive CGD (AR-CGD). Here, we present 5 patients with CGD developing LE at different ages to emphasize on the importance of appropriate follow-up and treatment in patients with CGD with clinical signs and symptoms of autoimmune diseases and even in those with negative serologic results.Entities:
Keywords: Chronic; Cutaneous; Granulomatous disease; Iran; Lupus erythematosus; Rare diseases
Year: 2019 PMID: 31522454 DOI: 10.18502/ijaai.v18i4.1426
Source DB: PubMed Journal: Iran J Allergy Asthma Immunol ISSN: 1735-1502 Impact factor: 1.464