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3.
J Dtsch Dermatol Ges ; 6(10): 861-4, 2008 Oct.
Artigo em Inglês, Alemão | MEDLINE | ID: mdl-18498380

RESUMO

SUMMARY: In a patient with foreign-body granulomas, dog hairs were identified as the causative agent by combing history, histopathology and highly sensitive detection of species-specific canine mitochondrial DNA. Granulomas from human hair are well known in hairdressers. Animal hair granulomas have so far been only described in dog groomers, milkers, and shearers. To the best of our knowledge this patient represents the first described case of dog hair granulomas in a pet owner.


Assuntos
Granuloma de Corpo Estranho/diagnóstico , Granuloma de Corpo Estranho/etiologia , Cabelo , Dermatopatias/diagnóstico , Dermatopatias/etiologia , Adulto , Animais , Cães , Humanos , Masculino , Doenças Raras , Zoonoses/transmissão
4.
J Clin Oncol ; 23(34): 8655-63, 2005 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-16260701

RESUMO

PURPOSE: The combination of interferon alfa (IFNalpha) and isotretinoin has shown a direct antiproliferative effect on human melanoma cell lines, but it remained unclear whether this combination is more effective than IFNalpha alone in patients with metastatic melanoma. We evaluated safety and efficacy of IFNalpha and isotretinoin compared with IFNalpha alone as adjuvant treatment in patients with primary malignant melanoma stage IIA and IIB. PATIENTS AND METHODS: In a prospective, randomized, double-blind, placebo-controlled trial, 407 melanoma patients in stage IIA (301 patients) and IIB (106 patients) were randomly assigned to either IFNalpha and isotretinoin (isotretinoin group; 206 patients) or IFNalpha and placebo (placebo group; 201 patients) after excision of the primary tumor. IFNalpha was administered three times a week at a dose of 3 million units subcutaneously for 24 months. Isotretinoin at a dose of 20 mg for patients < or = 73 kg, 30 mg for patients greater than 73 kg, or placebo daily for 24 months. RESULTS: A scheduled interim analysis revealed no significant differences in survival rates, with the isotretinoin group and the placebo group showing 5-year disease-free survival rates of 55% (95% CI, 46% to 65%) and 67% (95% CI, 59% to 75%), respectively, and overall 5-year survival rates of 76% (95% CI, 67% to 84%) and 81% (95% CI, 74% to 88%), respectively. The trial was stopped for futility. CONCLUSION: The addition of isotretinoin to an adjuvant treatment of low-dose IFNalpha in patients with stage IIA and IIB melanoma had no significant effect on disease-free or overall survival and is therefore not recommended.


Assuntos
Antineoplásicos/uso terapêutico , Neoplasias de Cabeça e Pescoço/tratamento farmacológico , Interferon-alfa/uso terapêutico , Isotretinoína/uso terapêutico , Melanoma/tratamento farmacológico , Adolescente , Adulto , Idoso , Antineoplásicos/efeitos adversos , Carcinoma Basocelular/tratamento farmacológico , Carcinoma Basocelular/secundário , Carcinoma de Células Escamosas/tratamento farmacológico , Carcinoma de Células Escamosas/secundário , Quimioterapia Adjuvante , Intervalo Livre de Doença , Método Duplo-Cego , Europa (Continente) , Feminino , Neoplasias de Cabeça e Pescoço/patologia , Humanos , Hiperlipidemias/induzido quimicamente , Interferon-alfa/efeitos adversos , Isotretinoína/efeitos adversos , Masculino , Melanoma/patologia , Pessoa de Meia-Idade , Análise Multivariada , Estadiamento de Neoplasias , Prognóstico , Estudos Prospectivos , Qualidade de Vida , Dermatopatias/induzido quimicamente , Resultado do Tratamento
5.
J Dtsch Dermatol Ges ; 3(12): 974-8, 2005 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16405713

RESUMO

BACKGROUND: Patients with gluten sensitivity, i. e. celiac disease and dermatitis herpetiformis have anti-endomysial antibodies recognizing transglutaminases, which are usually detected on appropriate tissue sections. It would be desirable to have available a reliable, tissue-independent serological diagnostic tool. We compared disease-specificity and sensitivity of tTG versus eTG-based detection systems for the diagnosis of anti-endomysial IgA-antibodies. PATIENTS AND METHODS: We examined 204 serum samples in duplicates with commercial human ELISA-kits: 54 healthy blood donors, 20 celiac disease, 29 dermatitis herpetiformis and 101 with other autoimmune dermatoses. RESULTS: The tTG-based ELISA proved to be very disease-specific (100 %) and sensitive for the diagnosis of gluten sensitivity (95 % celiac disease; 96.6 % dermatitis herpetiformis). The eTG-based ELISA was also perfectly specific (100 %), but only 15 % of celiac disease-sera and 44.8 % of dermatitis herpetiformis-sera yielded positive results. CONCLUSIONS: The human tTG-ELISA fulfills all criteria of a screening test and, because of being investigator-independent, inexpensive and highly reproducible, compares favorably with the current diagnostic gold standard (indirect immunofluorescence and biopsy) of celiac disease and dermatitis herpetiformis. The low sensitivity of the eTG-ELISA may have technical reasons, but could theoretically also be linked to disease activity or indicate the existence of an as yet undefined disease subset. Studies are currently under way to address these issues.


Assuntos
Doença Celíaca/sangue , Doença Celíaca/diagnóstico , Dermatite Herpetiforme/sangue , Dermatite Herpetiforme/diagnóstico , Ensaio de Imunoadsorção Enzimática/métodos , Transglutaminases/sangue , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Autoantígenos/sangue , Biomarcadores/sangue , Doença Celíaca/enzimologia , Dermatite Herpetiforme/enzimologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Reprodutibilidade dos Testes , Sensibilidade e Especificidade
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