Case Report of Acquired Generalized Lipodystrophy Associated With Common Variable Immunodeficiency

J Clin Endocrinol Metab. 2018 Aug 1;103(8):2807-2810. doi: 10.1210/jc.2018-00494.

Abstract

Context: Acquired generalized lipodystrophy (AGL), a rare disorder characterized by loss of subcutaneous adipose tissue, is estimated to occur in association with autoimmune diseases in ~25% of the cases. Common variable immunodeficiency (CVI) is a condition known for its strong association with autoimmune diseases often occurring with negative autoantibodies. To the best of our knowledge, we describe the first known case of AGL in a patient with CVI.

Case description: A 24-year-old man was referred to our center with hyperglycemia, hypertriglyceridemia, hepatomegaly, and a clear pattern of generalized fat loss. AGL had been diagnosed on the basis of the clinical and laboratory findings. Because of the presence of associated hypogammaglobulinemia, a diagnosis of CVI was subsequently established.

Conclusions: We propose that AGL be added to the list of possible diseases associated with CVI and, owing to the similar clinical presentation with type 1 diabetes mellitus, be included in the differential diagnosis of this condition, which is present in 1.5% of patients with CVI.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Common Variable Immunodeficiency / complications*
  • Humans
  • Hypertriglyceridemia / complications
  • Hypertriglyceridemia / immunology
  • Lipodystrophy / etiology*
  • Lipodystrophy / immunology
  • Male
  • Young Adult