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Topical 1% propranolol ointment with occlusion in treatment of pyogenic granulomas: An open-label study in 22
Iria Neri1, Carlotta Baraldi1, Riccardo Balestri1
1Section of Dermatology, Department of Experimental, Diagnostic and Specialty Medicine, Saint Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Insights
Topical propranolol ointment effectively treats pediatric pyogenic granuloma (PG), a common skin condition. Most cases resolved without side effects, suggesting a promising alternative to destructive therapies.
Area of Science:
- Dermatology
- Pediatrics
- Vascular Neoplasms
Background:
- Pyogenic granuloma (PG) is a frequent benign vascular tumor affecting skin and mucous membranes, primarily in children and adolescents.
- Current treatments for PG involve destructive methods, carrying risks of pain, scarring, and pigmentation changes.
Purpose of the Study:
- To evaluate the efficacy and safety of topical propranolol 1% ointment in treating pediatric cutaneous pyogenic granuloma.
Main Methods:
- A prospective, single-arm, open-label study was conducted.
- Children diagnosed with cutaneous PG received a compounded 1% propranolol ointment formulation.
- Treatment involved daily application with occlusion.
Main Results:
- Topical propranolol demonstrated significant efficacy, with 59.0% of patients achieving complete regression of PG.
- An additional 18.2% of patients showed stable disease, while 22.7% did not respond to treatment.
- No adverse side effects, including skin irritation, allergy, or bleeding, were reported during the study.
Conclusions:
- Topical propranolol ointment 1% with occlusion is an effective and safe treatment option for pediatric pyogenic granuloma.
- Early intervention with topical propranolol appears to correlate with improved treatment outcomes.
Background:
Pyogenic granuloma (PG) is a common, acquired, benign vascular neoplasm of the skin and mucous membranes. It occurs most often in children and adolescents. First-line treatment options for PG are based on destructive approaches. Pain, permanent scarring, and pigmentation are potential complications of these therapies.
Methods:
This single-arm, open-label, prospective study evaluated the efficacy of topical propranolol for treatment of PGs in children. All patients clinically diagnosed with cutaneous PG consecutively at the Dermatology Pediatric Outpatient Service of the University of Bologna from January 2010 to December 2010 received a compounded formulation of propranolol ointment 1%.
Results:
We found propranolol ointment to be effective in consecutive patients; 59.0% completely regressed in a mean of 66 days, 18.2% remained stable, and 22.7% did not respond. No side effects (eg, skin irritation, allergy, bleeding) were observed.
Conclusion:
Topical propranolol ointment 1% with occlusion appears to be an effective treatment for PGs in children. Early treatment was associated with a more favorable outcome.
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