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Published on: September 27, 2024
Facial angiofibromas treated with topical rapamycin: an excellent choice with fast response
Teresa Truchuelo1, Blanca Díaz-Ley, Luis Ríos
1Ramón y Cajal Hospital Madrid, Spain.
Abstract:
Tuberous sclerosis (TS) is the second most common genodermatosis in our country and one of its main characteristics is the presence of facial angiofibromas. These benign tumors can be really bothersome for some patients and there is not a gold-standard treatment. Laser therapy has been used with good responses but it is a painful option and recurrence is guaranteed. TS develops as a result of a mutation of one of two genes, TSC1 or TSC2, which encode for hamartin and tuberin, respectively. TSC1 and TSC2 are tumor suppressors that inhibit mTOR, which if mutated results in mTOR activation, leading to an increase in protein translation. This eventually induces formation of hamartomatous tumors in patients with TSC. Oral rapamycin had been reported to be effective for the treatment of various tumors, apparently because of its action of inhibiting the m-TOR complex. Recently it has been suggested that the drug may be effective when applied topically. We report the 6th case of facial AF treated with topical rapamycin, 1 percent, once per day. An excellent response was achieved surprisingly rapidly. We propose this option as a safe and effective therapy.
Insights
Topical rapamycin offers a safe and effective treatment for facial angiofibromas associated with tuberous sclerosis (TS). This therapy rapidly reduced tumors in a patient, presenting a promising alternative to painful laser treatments.
Area of Science:
- Dermatology
- Genetics
- Oncology
Background:
- Tuberous sclerosis (TS) is a common genodermatosis characterized by facial angiofibromas.
- Current treatments like laser therapy are painful and have high recurrence rates.
- TS is caused by mutations in TSC1 or TSC2 genes, leading to mTOR pathway activation and tumor formation.

