Tuberous sclerosis complex with autosomal dominant polycystic kidney disease: a rare duo

BMJ Case Rep. 2014 Dec 17:2014:bcr2014207471. doi: 10.1136/bcr-2014-207471.

Abstract

Tuberous sclerosis complex (TSC) is an autosomal dominant condition characterised by the presence of multiple hamartomas in various organ systems in the body. The kidneys are affected in 80% of patients, usually in the form of renal angiomyolipomas, renal cysts or renal cell carcinoma. Although extremely rare, TSC and autosomal dominant polycystic kidney disease (ADPKD) can co-exist in the same patient as a result of concurrent deletion of both polycystic kidney disease (PKD) 1 and TSC2 genes present on the chromosome 16p13.3. These patients develop end-stage renal disease at an earlier age and have an increased risk of malignancy. We present a case of a 30-year-old man with a history of tuberous sclerosis, presenting with loin pain and subsequently diagnosed to have ADPKD.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Chromosomes, Human, Pair 16*
  • Humans
  • Kidney / pathology*
  • Male
  • Mutation*
  • Polycystic Kidney, Autosomal Dominant / complications*
  • Polycystic Kidney, Autosomal Dominant / genetics
  • Renal Insufficiency / etiology
  • TRPP Cation Channels / genetics
  • Tuberous Sclerosis / complications*
  • Tuberous Sclerosis / genetics
  • Tuberous Sclerosis Complex 2 Protein
  • Tumor Suppressor Proteins / genetics

Substances

  • TRPP Cation Channels
  • TSC2 protein, human
  • Tuberous Sclerosis Complex 2 Protein
  • Tumor Suppressor Proteins
  • polycystic kidney disease 1 protein