Table 6:
Which isolated extra-renal findings should prompt consideration of genetic risk assessment?*
Consensus question | Yes | No |
---|---|---|
| ||
Independent of family history, should a patient with the following isolated extra-renal manifestation undergo genetic testing? | ||
| ||
A single hemangioblastoma (CNS and/or retina) | 48% | 52% |
| ||
A single pheochromocytoma or paraganglioma | 100% | 0% |
| ||
A single endolymphatic sac tumor | 100% | 0% |
| ||
A single cutaneous leiomyoma | 57% | 43% |
| ||
A history of spontaneous pneumothorax | 32% | 68% |
| ||
Skin fibrofolliculomas | 56% | 44% |
| ||
Uveal melanoma | 88% | 12% |
| ||
A single FH-deficient uterine fibroid | 93% | 7% |
Statements in bold represent those with reached consensus