The management of renal angiomyolipomas in a patient with tuberous sclerosis
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Published on: June 15, 2020
Ilene Y Wong1, Linda D Shortliffe
1Department of Urology, Stanford University School of Medicine, Stanford, CA 94305-5118, USA.
Insights
Tuberous sclerosis can cause large bilateral renal angiomyolipomas. This case highlights observation and embolization as management strategies for these tumors.
Area of Science:
- Nephrology
- Oncology
- Genetics
Background:
- Tuberous sclerosis is a genetic disorder.
- It can lead to the development of tumors in various organs, including the kidneys.
Observation:
- A 17-year-old female with tuberous sclerosis presented with multiple bilateral renal masses.
- The largest mass measured 6.0 cm in diameter on the left side.
- Diagnostic workup included physical examination, ultrasonography, MRI, CT, and magnetic resonance angiography.
Findings:
- Bilateral renal angiomyolipomas were diagnosed.
- Serial creatinine levels were monitored.
Implications:
- Management involved observation, serial imaging, and embolization with infarction.
- This case underscores the importance of vigilant monitoring and tailored treatment for renal angiomyolipomas in patients with tuberous sclerosis.
Background:
A 17-year-old girl, who was diagnosed with tuberous sclerosis in infancy, presented with multiple bilateral renal masses, the largest of which was 6.0 cm in diameter on the left side.
Investigations:
History and physical examination, ultrasonography, MRI, CT, magnetic resonance angiography, and measurement of serial creatinine levels.
Diagnosis:
Bilateral angiomyolipomas.Management Observation, serial imaging, embolization and infarction.
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