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Efficacy and Safety of Topical Corticosteroid Treatment under Occlusion for Severe Alopecia Areata in Children. A single-center retrospective analysis.
Lee, Young Yoon; Lim, Han Hyuk; Son, Seungjin; Jin, Soyoung; Shin, Jung-Min; Hong, Dong-Kyun; Jung, Kyung Eun; Seo, Young-Joon; Lee, Tae Kwan; Kim, Yoo-Mi; Lee, Young.
Affiliation
  • Lee YY; Department of Dermatology and Chungnam National University, Daejeon, Republic of Korea.
  • Lim HH; Department of Pediatrics, School of Medicine, Chungnam National University, Daejeon, Republic of Korea.
  • Son S; Department of Dermatology and Chungnam National University, Daejeon, Republic of Korea.
  • Jin S; Department of Dermatology and Chungnam National University, Daejeon, Republic of Korea.
  • Shin JM; Department of Dermatology and Chungnam National University, Daejeon, Republic of Korea.
  • Hong DK; Department of Dermatology and Chungnam National University, Daejeon, Republic of Korea.
  • Jung KE; Department of Dermatology and Chungnam National University, Daejeon, Republic of Korea.
  • Seo YJ; Department of Dermatology and Chungnam National University, Daejeon, Republic of Korea.
  • Lee TK; Department of Pediatrics, School of Medicine, Chungnam National University, Daejeon, Republic of Korea.
  • Kim YM; Department of Pediatrics, School of Medicine, Chungnam National University, Daejeon, Republic of Korea.
Clin Exp Dermatol ; 2024 Mar 19.
Article in En | MEDLINE | ID: mdl-38501938
ABSTRACT

BACKGROUND:

Alopecia areata (AA) has a poor clinical course in children. There are no reliable therapeutic options for children with severe AA, including alopecia totalis (AT) and alopecia universalis (AU).

AIM:

We evaluated the efficacy and adverse effects of a potent topical corticosteroid (TCS) under occlusion in pediatric patients with severe AA.

METHODS:

We reviewed records of 23 patients under the age of 10 years with AT or AU treated with a potent TCS (0.05% clobetasol propionate or 0.3% diflucortolone valerate) for 8 hours under occlusion with a plastic film. We used the Severity of Alopecia Tool (SALT) to measure clinical improvement. The primary endpoint was a Severity of Alopecia Tool (SALT) score of 20 or less at six months. We analyzed the change in cortisol levels to identify the long-term safety of TCS therapy on the hypothalamus-pituitary-adrenal axis.

RESULTS:

Nineteen patients reached SALT 20 or less at the 6-month treatment. Six patients relapsed over the 6-month follow-up period. Four patients were suspected of adrenal insufficiency. However, the cortisol level of the patients recovered to normal at least 1-month after lowering TCS potency or changing to non-steroidal treatments.

LIMITATIONS:

Retrospective design and small sample size.

CONCLUSION:

This study shows that a potent TCS occlusion may be a safe treatment option in pediatric patients with severe AA. Further long-term studies are required to evaluate the safety and recurrence of TCS occlusion therapy for pediatric AA.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Clin Exp Dermatol Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Clin Exp Dermatol Year: 2024 Document type: Article
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