Mechanisms of kidney disease in Sneddon's syndrome: Case report and literature review

Clin Nephrol. 2020 Apr;93(4):209-214. doi: 10.5414/CN109748.

Abstract

Sneddon's syndrome is a rare, noninflammatory thrombotic vasculopathy characterized by the combination of livedo racemosa, recurrent stroke, and histopathological skin lesions of endarteritis obliterans. Although multiorgan involvement suggests its systemic nature, detailed pathological description of affected organs - including the kidney - is exceptional. We report a case of Sneddon's syndrome with chronic kidney disease, associated with features of endarteritis obliterans in the skin and the kidney. The clinical presentation of our patient is compared to previously reported cases of Sneddon's syndrome with biopsy-proven kidney disease. We also discuss the differential diagnosis, pathophysiological mechanisms, relationship with antiphospholipid syndrome, and management of patients with Sneddon's syndrome and kidney disease. This clinical observation supports the systemic nature of Sneddon's syndrome and provides insights into the mechanisms by which this rare but probably underdiagnosed disease alters kidney function. .

Publication types

  • Case Reports
  • Review

MeSH terms

  • Female
  • Humans
  • Middle Aged
  • Renal Insufficiency, Chronic / etiology*
  • Sneddon Syndrome / complications*