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1.
Pediatr Dermatol ; 41(3): 515-517, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-38387093

RESUMEN

We report a case of congenital multisystem Langerhans cell histiocytosis with cutaneous and hematopoietic involvement. After the failure of first-line (vinblastine and prednisolone) and second-line (vincristine and cytarabine) therapies, treatment with cobimetinib, a mitogen-activated protein kinase (MEK) inhibitor, led to the remission of disease and a sustained response after 11 months of ongoing treatment. Protein kinase inhibitors targeting BRAF or MEK could represent a promising future therapeutic option, also in children with LCH.


Asunto(s)
Azetidinas , Histiocitosis de Células de Langerhans , Piperidinas , Humanos , Histiocitosis de Células de Langerhans/tratamiento farmacológico , Histiocitosis de Células de Langerhans/congénito , Azetidinas/uso terapéutico , Piperidinas/uso terapéutico , Inhibidores de Proteínas Quinasas/uso terapéutico , Masculino , Femenino , Lactante
3.
Clin Drug Investig ; 43(4): 299-306, 2023 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-37012527

RESUMEN

BACKGROUND: Tralokinumab, the first fully human monoclonal antibody that binds specifically to interleukin-13, was safe and effective for treating atopic dermatitis (AD) in clinical trials, but real-life experience is still limited. OBJECTIVES: The objective of this study was to evaluate the effectiveness and safety of tralokinumab in severe AD in a real-life multicenter prospective cohort. METHODS: Adult patients with severe AD were enrolled between January 2022 and July 2022 and received tralokinumab subcutaneously for 16 weeks. Objective and subjective scores were collected at baseline, weeks 6 and 16. Adverse events were reported throughout the study. RESULTS: Twenty-one patients were included. An improvement of at least 75% on the Eczema Area and Severity Index (EASI 75) was achieved in 66.7% of patients at week 16. The median objective and subjective scores at week 16 were significantly (p < 0.001) lower than those at baseline. Combination with cyclosporine was sometimes necessary at the beginning of treatment, and addition of upadacitinib was required for some patients with very severe disease during the treatment. The most frequent adverse events were flares of eczema (23.8%) and reactions at injection site (19.0%). No cases of conjunctivitis were reported. Four patients (19.0%) discontinued treatment. CONCLUSIONS: Tralokinumab is an effective first-line biotherapy for severe AD. However, therapeutic response may be progressive. Safety data were reassuring. Atopic dermatitis flares or reactions at the injection site may lead to discontinuation of treatment. A history of conjunctivitis on dupilumab is not a contraindication to the initiation of tralokinumab.


Asunto(s)
Conjuntivitis , Dermatitis Atópica , Eccema , Humanos , Adulto , Estudios Prospectivos , Dermatitis Atópica/diagnóstico , Dermatitis Atópica/tratamiento farmacológico , Resultado del Tratamiento , Inyecciones Subcutáneas , Método Doble Ciego , Anticuerpos Monoclonales/efectos adversos , Índice de Severidad de la Enfermedad , Conjuntivitis/inducido químicamente , Conjuntivitis/tratamiento farmacológico , Eccema/inducido químicamente , Eccema/tratamiento farmacológico
4.
Pediatr Dermatol ; 36(3): 365-367, 2019 May.
Artículo en Inglés | MEDLINE | ID: mdl-30859627

RESUMEN

We report a case of benign lymphoplasmacytic plaque (LPP) in a child. These asymptomatic erythematous papulonodular lesions are an emerging clinicopathological entity. Herein, we describe a previously unreported site for LPP lesions, namely, the volar wrist and the distal ipsilateral palm.


Asunto(s)
Seudolinfoma/diagnóstico , Seudolinfoma/terapia , Enfermedades de la Piel/diagnóstico , Enfermedades de la Piel/terapia , Preescolar , Humanos , Masculino , Seudolinfoma/etiología , Enfermedades de la Piel/etiología
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