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CASE REPORT
Hereditary leiomyomatosis and renal cell cancer (HLRCC): cutaneous and renal manifestations requiring a multidisciplinary team approach
  1. Agnieszka Adams1,
  2. Kendall Katie Sharpe2,3,
  3. Peter Peters4,
  4. Michael Freeman5
  1. 1 Royal Australian College of General Practitioners, Graceville, Australia
  2. 2 Department of Otolaryngology, Sir Charles Gairdner Hospital, Nedlands, Australia
  3. 3 Department of Medical Education, Gold Coast Hospital and Health Service, Southport, Australia
  4. 4 Gold Coast University Hospital, Gold Coast, Australia
  5. 5 Department of Dermatology, Gold Coast Hospital and Health Service, Southport, Australia
  1. Correspondence to Dr Kendall Katie Sharpe, kendycakes{at}hotmail.com

Summary

Cutaneous leiomyomasare rare tumours of smooth muscle origin associated with disorders such as hereditary leiomyomatosis and renal cell cancer (HLRCC) syndrome. HLRCC is an autosomal dominant syndrome caused by loss of function mutations in the fumarate hydratase gene. Sufferers of this disorder are predisposed to the development of tumours of the skin and/or uterus, with a further subset of HLRCC families at risk of renal cell carcinoma with papillary features. This syndrome is rare and carries with it a significant rate of mortality. A multidisciplinary approach to care is critical in the management of these patients and their families. The dermatologist can play a central role in this process, coordinating care between specialist medical and allied health teams.

  • Dermatology
  • Obstetrics and gynaecology
  • Urology

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Footnotes

  • Contributors KKS confirms that all authors have contributed equally to the preparation of this manuscript with regard to patient care, research and writing.

  • Competing interests None declared.

  • Patient consent Obtained.

  • Provenance and peer review Not commissioned; externally peer reviewed.