Pearls and pitfalls: Autoimmune lymphoproliferative syndrome and autoimmune lymphoproliferative syndrome-like disease

Allergy Asthma Proc. 2017 Jul 1;38(4):317-321. doi: 10.2500/aap.2017.38.4062.

Abstract

A case of autoimmune lymphoproliferative syndrome (ALPS) was presented, followed by a discussion of the clinical characteristics, pathophysiology, diagnosis, and management of this disease. Clinical pearls and pitfalls are emphasized for the use of the practicing allergist and the fellow in-training. The diagnosis of ALPS was guided by published criteria. A careful history and workup were needed to exclude other possible etiologies for the patient's symptoms and physical findings. ALPS often carries significant morbidity and is best managed through a multidisciplinary approach.

Publication types

  • Case Reports

MeSH terms

  • Autoimmune Diseases / diagnosis*
  • Autoimmune Diseases / epidemiology
  • Autoimmune Lymphoproliferative Syndrome / diagnosis*
  • Autoimmune Lymphoproliferative Syndrome / genetics
  • Autoimmune Lymphoproliferative Syndrome / immunology
  • Autoimmune Lymphoproliferative Syndrome / therapy
  • DNA Mutational Analysis
  • Diagnosis, Differential
  • Genetic Predisposition to Disease
  • Humans
  • Male
  • Mutation
  • Phenotype
  • Predictive Value of Tests
  • Young Adult
  • fas Receptor / genetics

Substances

  • FAS protein, human
  • fas Receptor