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Recurrent haematospermia: an unusual presentation of autosomal dominant polycystic kidney disease
  1. Vivek Sood1,
  2. Viswanadh Bhairavabhatla2,
  3. Somali Pattanayak3 and
  4. Vishal Singh1
  1. 1Nephrology, Army Hospital Research and Referral, New Delhi, India
  2. 2Medicine, Army Hospital Research and Referral, New Delhi, India
  3. 3Radiodiagnosis, Army Hospital Research and Referral, New Delhi, India
  1. Correspondence to Dr Vivek Sood; viverit{at}gmail.com

Abstract

Haematospermia, even though alarming, is usually benign and self-limiting, especially in a sexually active male. Nevertheless recurrent, refractory or painful haematospermia is troublesome and warrants thorough evaluation. In this context, we describe a rare case of recurrent haematospermia whereby evaluation revealed haemorrhage in seminal vesicle cysts and consequently established the aetiology of autosomal dominant polycystic kidney disease.

  • Hematuria
  • Urinary tract infections

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Footnotes

  • Contributors VSd: patient management, manuscript editing, figure 3. VB: manuscript writing. SP: imaging and manuscript writing. VSh: patient management, manuscript editing.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Case reports provide a valuable learning resource for the scientific community and can indicate areas of interest for future research. They should not be used in isolation to guide treatment choices or public health policy.

  • Competing interests None declared.

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