Malignant nephrosclerosis in a patient with familial Mediterranean fever

Intern Med. 2015;54(20):2643-6. doi: 10.2169/internalmedicine.54.4937. Epub 2015 Oct 15.

Abstract

A 37-year-old man was admitted to our hospital for an evaluation of renal dysfunction and hypertension. The C-reactive protein level was 6.0 mg/dL, and the serum renin activity was extremely high. A renal biopsy showed malignant nephrosclerosis-like lesions with an onion skin pattern. He had a history of recurrent abdominal pain associated with periodic fevers above 38 degrees that resolved within three days. A MEditerranean FeVer (MEFV) gene analysis revealed that he was homozygous for the E148Q polymorphism (exon 2) and heterozygous for the L110P polymorphism (exon 2). The present case demonstrates that persistent subclinical inflammation can lead to malignant nephrosclerosis in familial Mediterranean fever patients with this genotype.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abdominal Pain / complications
  • Adult
  • C-Reactive Protein / analysis
  • Familial Mediterranean Fever / complications*
  • Familial Mediterranean Fever / genetics*
  • Fever / complications
  • Genotype
  • Humans
  • Inflammation / complications
  • Male
  • Nephrosclerosis / complications
  • Nephrosclerosis / etiology*
  • Polymorphism, Genetic
  • Renin / blood

Substances

  • C-Reactive Protein
  • Renin