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1.
An Bras Dermatol ; 92(5 Suppl 1): 126-128, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-29267469

RESUMEN

Epidermolysis bullosa is a group of mechano-bullous genetic disorders caused by mutations in the genes encoding structural proteins of the skin. Dystrophic epidermolysis bullosa is caused by mutations in the COL7A1 gene encoding collagen VII, the main constituent of anchoring fibrils. In this group, there are autosomal dominant and recessive inheritances. The pre-tibial form is characterized by the presence of blisters, milia, atrophic scars and lesions similar to lichen planus. The diagnosis is clinical and laboratory and subtypes are distinguished by means of immunohistochemical and ultrastructural studies, in addition to genetic differentiation. Electron microscopy and immunomapping are used in the diagnosis.


Asunto(s)
Epidermólisis Ampollosa Distrófica/patología , Adulto , Vesícula/patología , Diagnóstico Diferencial , Femenino , Humanos , Inmunohistoquímica , Prurito/patología
2.
An Bras Dermatol ; 92(1): 134-136, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28225975

RESUMEN

This is a retrospective study of 160 patients treated in private practice in São Paulo from March 2003 to March 2015. We analyzed 171 results of direct mycological examinations and fungal cultures from nail scrapings. The agreement between direct mycological examination results and fungal culture was satisfactory, consistent with the literature (kappa 0.603). The main agent identified was Trichophyton rubrum (51%). We observed an isolation rate of non-dermatophyte filamentous fungi superior to the literature (34%). Determining the agent is key to defining the appropriate onychomycosis treatment, and knowing the epidemiology of patients treated in private practice helps the dermatologist who works in this context.


Asunto(s)
Onicomicosis/microbiología , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad , Práctica Privada , Estudios Retrospectivos
3.
An. bras. dermatol ; 92(1): 134-136, Jan.-Feb. 2017. tab, graf
Artículo en Inglés | LILACS | ID: biblio-1038242

RESUMEN

ABSTRACT This is a retrospective study of 160 patients treated in private practice in São Paulo from March 2003 to March 2015. We analyzed 171 results of direct mycological examinations and fungal cultures from nail scrapings. The agreement between direct mycological examination results and fungal culture was satisfactory, consistent with the literature (kappa 0.603). The main agent identified was Trichophyton rubrum (51%). We observed an isolation rate of non-dermatophyte filamentous fungi superior to the literature (34%). Determining the agent is key to defining the appropriate onychomycosis treatment, and knowing the epidemiology of patients treated in private practice helps the dermatologist who works in this context.


Asunto(s)
Humanos , Masculino , Femenino , Persona de Mediana Edad , Anciano , Onicomicosis/microbiología , Práctica Privada , Estudios Retrospectivos
4.
An. bras. dermatol ; 92(5,supl.1): 126-128, 2017. graf
Artículo en Inglés | LILACS | ID: biblio-887097

RESUMEN

Abstract Epidermolysis bullosa is a group of mechano-bullous genetic disorders caused by mutations in the genes encoding structural proteins of the skin. Dystrophic epidermolysis bullosa is caused by mutations in the COL7A1 gene encoding collagen VII, the main constituent of anchoring fibrils. In this group, there are autosomal dominant and recessive inheritances. The pre-tibial form is characterized by the presence of blisters, milia, atrophic scars and lesions similar to lichen planus. The diagnosis is clinical and laboratory and subtypes are distinguished by means of immunohistochemical and ultrastructural studies, in addition to genetic differentiation. Electron microscopy and immunomapping are used in the diagnosis.


Asunto(s)
Humanos , Femenino , Adulto , Epidermólisis Ampollosa Distrófica/patología , Prurito/patología , Inmunohistoquímica , Vesícula/patología , Diagnóstico Diferencial
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