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Chromoblastomycosis: tissue modifications during itraconazole treatment

BACKGROUND: Histological and mycological changes during itraconazole use have not been totally established in chromoblastomycosis. OBJECTIVES: To evaluate tissue modifications in chromoblastomycosis carriers under itraconazole treatment. METHODS: A histological retrospective study of 20 cases of chr...

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Detalles Bibliográficos
Autores principales: Purim, Kátia Sheylla Malta, Peretti, Murilo Calvo, Fillus Neto, José, Olandoski, Marcia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595593/
https://www.ncbi.nlm.nih.gov/pubmed/28954095
http://dx.doi.org/10.1590/abd1806-4841.20175466
Descripción
Sumario:BACKGROUND: Histological and mycological changes during itraconazole use have not been totally established in chromoblastomycosis. OBJECTIVES: To evaluate tissue modifications in chromoblastomycosis carriers under itraconazole treatment. METHODS: A histological retrospective study of 20 cases of chromoblastomycosis seen at the university hospital at the south of Brazil, during itraconazole 400 mg daily treatment. Patients were classified into two groups: plaque or tumor lesions, and underwent periodic evaluations every four months during three years. Hematoxylin-eosin stain was used to analyze epidermal modifications, inflammatory infiltrate and fibrosis, and Fontana-Masson stain for parasite evaluation. RESULTS: Fontana-Masson stain was superior to hematoxylin-eosin stain in fungal count in the epidermis (mean difference=0.14; p<0.05). The most distinct mycosis tissue responses were registered in the dermis. Epidermal thinning, granulomatous infiltrate decrease or disappearance, fibrosis increase and quantitative/morphological changes occurred during treatment. STUDY LIMITATIONS: Patients could not be located to have their current skin condition examined. CONCLUSION: Parasitic and tissue changes verified in this study can reflect the parasite-host dynamics under itraconazole action.