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1.
J Eur Acad Dermatol Venereol ; 37(12): 2601-2607, 2023 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-37620285

RESUMO

BACKGROUND: Kligman's trio (KT), combining hydroquinone, retinoic acid and corticosteroid, is considered as the gold standard treatment of melasma. Its efficacy has never been matched before, but it is tempered by frequent adverse effects. OBJECTIVE: To assess the efficacy and tolerance of a New Trio (NT) combination with isobutylamido-thiazolyl-resorcinol, retinoic acid and cortosteroid compared to KT. METHODS: We conducted a 24-week monocentric trial, randomized, double-blind, controlled versus KT, with 40 melasma patients. NT and KT were applied for 12 weeks and associated with the same sunscreen applied for 24 weeks. The primary endpoint was the modified Melasma Area Severity Index (mMASI) at 12 weeks. Patient quality of life was investigated using MelasQoL. RESULTS: After 12 weeks, KT and NT groups both demonstrated a significant improvement in mMASI, respectively -2.84 (SE 0.69, p < 0.0002) and -4.33 (SE 0.71, p < 0.0001). The mean difference between the two groups was -1.49 (IC 95% -3.52 to 0.54, p = 0.14). MelasQoL improvement was -6.66 (SE 3.29, p = 0.0515) with KT and -12.57 (SE 3.29, p = 0.0006) with NT. CONCLUSION: The NT combination appears to be an effective treatment option for treating melasma and could be considered as a well-tolerated alternative to KT.


Assuntos
Melanose , Qualidade de Vida , Humanos , Estudos Prospectivos , Tretinoína/efeitos adversos , Resultado do Tratamento , Emolientes , Melanose/tratamento farmacológico , Hidroquinonas/efeitos adversos
2.
Arch Pediatr ; 28(1): 101-103, 2021 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-33250331

RESUMO

Beta thalassemias are autosomal recessive hemoglobin disorders related to a defect in the beta-globin chain production. Most of the major forms of beta-thalassemia are transfusion dependent leading to iron overload. Today, three iron chelators are available in France. We report the case of a patient suffering from ß+ major transfusion-dependent thalassemia who presented with severe skin reactions to deferoxamine and deferasirox as well as with agranulocytosis after deferiprone administration. The patient benefited from successful tolerance induction to deferasirox. With the increasing number of children suffering from iron overload, we believe that our protocol can be useful to pediatric hematology teams confronted with multiple iron chelator reactions.


Assuntos
Deferasirox/efeitos adversos , Dessensibilização Imunológica/métodos , Toxidermias/terapia , Quelantes de Ferro/efeitos adversos , Talassemia beta/tratamento farmacológico , Pré-Escolar , Deferasirox/uso terapêutico , Toxidermias/etiologia , Humanos , Tolerância Imunológica , Lactente , Quelantes de Ferro/uso terapêutico , Talassemia beta/imunologia
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