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1.
Dermatol Ther ; 33(6): e14250, 2020 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-32860461

RESUMEN

The association between urticaria and different virus infections has been reported in many studies. Different virus infections have been reported to be comorbidities of spontaneous urticaria. In this paper, we report the case of a male patient with acute urticaria 7 days after he left the hospital where he was treated for coronavirus disease 2019 (COVID-19). This infection may act as a causative or a facilitating factor for the initiation of acute urticaria and additional cofactors such as stress may contribute for the urticaria phenotype to be expressed. Additional facts for severe acute respiratory syndrome coronavirus 2 (SARS-COV-2) virus in future will clarify if urticarial rash is one of the COVID's multiple faces.


Asunto(s)
COVID-19/virología , SARS-CoV-2/patogenicidad , Urticaria/virología , Enfermedad Aguda , Antivirales/uso terapéutico , COVID-19/complicaciones , COVID-19/diagnóstico , Interacciones Huésped-Patógeno , Humanos , Masculino , Persona de Mediana Edad , Factores de Riesgo , SARS-CoV-2/efectos de los fármacos , Urticaria/diagnóstico , Tratamiento Farmacológico de COVID-19
2.
Dermatol Ther ; 33(2): e13255, 2020 03.
Artículo en Inglés | MEDLINE | ID: mdl-32031728

RESUMEN

Wegener's granulomatosis, is a rare form of systemic vasculitis characterized by necrotic granulomas around the blood vessels. We report a case of a healthy 43-year-old man presented with multiple ulcerated lesions in head and all over the body, that has appeared spontaneously. It was characterized by a giant deep ulceration covered by thick purulent, in size from 3 to 4 cm, deep; sub febrile temperature, and minimal pain associated. Skin biopsies results pyoderma gangrenosum (PG)-like features: anti-neutrophil cytoplasmic antibody (cANCA) positive. Six months later, the patient developed dispea episodes. CT scan (CT) result with multiple focal opacities. He was diagnosed with wegener granulomatosis (WG) and was treated with corticosteroids and ciclophosphamide. Skin involvement in WG is not common and lesions in the skin vary from purpura, paniculitis to ulceration. In our case, skin elements are the first manifestations. Whether these elements are Wegener manifestation or we have coexistence of PG with WG, it remains a still uncertain question to answer. There is no histopathologic pathognomic elements for both. Skin involvement in WG with PG-like lesions have been rarely reported. In front of this type of widespread ulcerations, resistant to treatment we should be aware that one of the reasons may be a disease of autoimmune etiology such as WG.


Asunto(s)
Granulomatosis con Poliangitis , Piodermia Gangrenosa , Úlcera Cutánea , Adulto , Granulomatosis con Poliangitis/complicaciones , Granulomatosis con Poliangitis/diagnóstico , Granulomatosis con Poliangitis/tratamiento farmacológico , Humanos , Masculino , Piodermia Gangrenosa/diagnóstico , Piodermia Gangrenosa/tratamiento farmacológico , Piel , Úlcera Cutánea/diagnóstico , Úlcera Cutánea/tratamiento farmacológico , Úlcera Cutánea/etiología , Úlcera
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