Successful treatment with secukinumab of psoriasis-like dermatitis in a patient with holocarboxylase synthetase deficiency.
Haifei LiuRuoqu WeiYijun YangZhen ZhangYixuan YangJue TangJiawen ChenJia ZhangYan GuZhirong YaoPublished in: The Journal of dermatology (2022)
Holocarboxylase synthetase deficiency (HSD) is a rare autosomal recessive disorder of biotin metabolism. Typical manifestations include irreversible metabolic disorders and erythroderma-like dermatitis. Most patients respond well to biotin supplementation. Psoriasis-like phenotype associated with this disease has been rarely reported in the literature and experiences with the use of biologics in patients with HSD are still lacking. We reported a rare case of recurrent psoriasis-like skin lesions in a 6-year-old child with HSD. The patient did not respond to initial therapy with high-dose oral biotin. Immunofluorescence staining showed an increased number of interleukin (IL)-17A+ cells in his skin lesions. Based on this finding, the patient was successfully treated with human anti-IL-17A monoclonal antibody (secukinumab). He did not report any side effects and remained healthy during the 2-year follow-up. We provide a comprehensive review of the reported cases of HSD with psoriasis-like dermatitis to date. The psoriasis-like phenotype of HSD is controversial in treatment and IL-17A inhibitor is an alternative therapeutic option.
Keyphrases
- atopic dermatitis
- monoclonal antibody
- high dose
- rare case
- case report
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- mental health
- newly diagnosed
- induced apoptosis
- ejection fraction
- ankylosing spondylitis
- chronic kidney disease
- low dose
- prognostic factors
- peritoneal dialysis
- stem cells
- bone marrow
- signaling pathway
- oxidative stress
- autism spectrum disorder
- duchenne muscular dystrophy
- combination therapy
- pi k akt
- pluripotent stem cells