Improvement of cystic fibrosis during treatment with isotretinoin
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Jennifer L Buckley1, Mark A Chastain, Robert L Rietschel
1Department of Dermatology, Tulane University School of Medicine, New Orleans, LA, USA.
Insights
Isotretinoin therapy for acne vulgaris in a cystic fibrosis patient showed potential benefits for reducing lung secretions and preventing respiratory infections. Further research is warranted to explore this unexpected finding in CF patients.
Area of Science:
- Dermatology
- Pulmonology
- Pharmacology
Background:
- A 15-year-old male with a history of recurrent respiratory infections presented with acne vulgaris.
- Standard acne treatments were ineffective, and the patient was subsequently diagnosed with cystic fibrosis (CF).
Observation:
- The patient was treated with isotretinoin for severe acne.
- During isotretinoin therapy, the patient experienced reduced lung secretions and fewer respiratory infections.
- Acne resolved, and these benefits persisted during subsequent treatment cycles.
Findings:
- Isotretinoin treatment led to significant acne clearance.
- A notable decrease in bronchopulmonary secretions and a reduction in antibiotic-requiring respiratory infections were observed during isotretinoin use.
- These positive pulmonary effects were associated with isotretinoin therapy in this CF patient.
Implications:
- Isotretinoin may offer a potential therapeutic benefit beyond acne treatment in cystic fibrosis patients.
- The observed reduction in respiratory symptoms warrants further investigation into the mechanisms of isotretinoin in CF.
- This case highlights a potential link between retinoid therapy and improved pulmonary outcomes in cystic fibrosis.
Abstract:
A 15-year-old boy with a history significant for multiple respiratory infections since birth presented for evaluation of acne vulgaris. He was initially prescribed doxycycline, topical tretinoin, and topical clindamycin solution, with the later addition of a benzoyl peroxide preparation to his regimen. The patient returned 6 months later after having been diagnosed with CF (cystic fibrosis) by sweat testing and genetic testing. His skin condition had not responded adequately to prior therapy, so all acne medications were discontinued. The 84-kg patient was started on 80 mg (0.95 mg/kg/d) of isotretinoin (13-cis-retinoic acid) daily. The patient's dose was decreased to 40 mg/d 2 weeks later following an episode of blood in his stool and epistaxis. At the 1- and 2-month follow-up visits, the patient reported improvement in his acne and mentioned that his lung secretions seemed reduced. His acne cleared after 4 months of therapy, so the isotretinoin was discontinued. The patient and his mother noted that no respiratory infections had occurred during the course of therapy. The patient's acne relapsed nearly 2 years later, so isotretinoin was restarted at 60 mg/d. During the next 7 months while on the drug, he experienced no further episodes of epistaxis or bloody stools and his acne had resolved by the end of therapy. The patient and his mother again reported fewer bronchopulmonary secretions and no infections requiring antibiotics during treatment with isotretinoin. This was unusual because he had experienced numerous respiratory infections requiring antibiotics during the prior 2 years. Since discontinuing the drug, the patient has had intermittent pulmonary infections and exacerbations in the symptomatology of his CF.
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