Related Experiment Videos

[Congenital pelvic arteriovenous fistula in a male. A case report]

H Mimata1, T Tanigawa, M Imagawa

  • 1Department of Urology, Medical College of Oita.

Insights

Congenital arteriovenous fistula in the male pelvis is rare. This case highlights diagnosis and management challenges for pelvic AV fistulas involving the bladder, prostate, and rectum.

Area of Science:

  • Urology
  • Vascular Surgery
  • Radiology

Background:

  • Congenital arteriovenous fistulas (AV fistulas) are rare vascular malformations.
  • Pelvic AV fistulas, particularly in males, are exceptionally uncommon.
  • This case focuses on a congenital AV fistula in the true pelvis.

Observation:

  • The patient presented with symptoms of pollakiuria (frequent urination) and intrarectal discomfort.
  • Diagnostic imaging included computed tomography (CT), magnetic resonance imaging (MRI), and cine angiography.
  • The AV fistula involved critical pelvic structures: bladder, prostate, and rectum.

Findings:

  • Diagnosis was confirmed via advanced imaging techniques.
  • Surgical intervention involved ligation of the main feeding arteries supplying the fistula.
  • The patient also had benign prostatic hypertrophy, managed conservatively due to high surgical bleeding risks.

Implications:

  • This case underscores the diagnostic and therapeutic complexities of rare congenital pelvic AV fistulas.
  • Conservative management of comorbidities like benign prostatic hypertrophy is crucial in high-risk surgical patients.
  • Successful management requires a multidisciplinary approach involving urology, radiology, and vascular surgery.

Related Concept Videos