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Artículo

The role of inherited and acquired factors in the development of porphyria cutanea tarda in the Argentinean population

Méndez, Manuel; Rossetti, Maria VictoriaIcon ; Batlle, Alcira María del C.Icon ; Parera, Victoria EstelaIcon
Fecha de publicación: 03/2005
Editorial: Mosby-Elsevier
Revista: Journal of the American Academy of Dermatology
ISSN: 0190-9622
Idioma: Inglés
Tipo de recurso: Artículo publicado
Clasificación temática:
Otras Ciencias Químicas

Resumen

Background: Inherited and environmental factors are implicated in the expression of porphyria cutanea  tarda (PCT); the contribution of each factor depends on the population.Inherited and environmental factors are implicated in the expression of porphyria cutanea  tarda (PCT); the contribution of each factor depends on the population. Objective: To provide a review of PCT cases diagnosed in Argentina over 24 years and evaluate the role of different precipitating factors in its pathogenesis.To provide a review of PCT cases diagnosed in Argentina over 24 years and evaluate the role of different precipitating factors in its pathogenesis. Methods: Plasma and urinary porphyrin levels and erythrocyte uroporphyrinogen decarboxylase (URO-D) activity were determined. Potential precipitating factors were identified in each patient. Additional tests for hepatitis C virus (HCV) and hemochromatosis gene mutations were carried out.Plasma and urinary porphyrin levels and erythrocyte uroporphyrinogen decarboxylase (URO-D) activity were determined. Potential precipitating factors were identified in each patient. Additional tests for hepatitis C virus (HCV) and hemochromatosis gene mutations were carried out. Results: Several factors (mainly alcohol abuse in men and estrogen ingestion in women), alone or combined were identified in our patients. Prevalence of HCV infection was 35.2%. Inherited URO-D deficiency occurs in 25.0% of cases. H63D was the most common hemochromatosis gene mutation. High incidence of PCT associated with HIV infection was found. Conclusions: PCT is multifactorial. Therefore, knowledge of all risk factors in each patient is important for the management of the disease. ( J Am Acad Dermatol 2005;52:417-24.) combined were identified in our patients. Prevalence of HCV infection was 35.2%. Inherited URO-D deficiency occurs in 25.0% of cases. H63D was the most common hemochromatosis gene mutation. High incidence of PCT associated with HIV infection was found. Conclusions: PCT is multifactorial. Therefore, knowledge of all risk factors in each patient is important for the management of the disease. ( J Am Acad Dermatol 2005;52:417-24.) combined were identified in our patients. Prevalence of HCV infection was 35.2%. Inherited URO-D deficiency occurs in 25.0% of cases. H63D was the most common hemochromatosis gene mutation. High incidence of PCT associated with HIV infection was found. Conclusions: PCT is multifactorial. Therefore, knowledge of all risk factors in each patient is important for the management of the disease. ( J Am Acad Dermatol 2005;52:417-24.) combined were identified in our patients. Prevalence of HCV infection was 35.2%. Inherited URO-D deficiency occurs in 25.0% of cases. H63D was the most common hemochromatosis gene mutation. High incidence of PCT associated with HIV infection was found. Conclusions: PCT is multifactorial. Therefore, knowledge of all risk factors in each patient is important for the management of the disease. ( J Am Acad Dermatol 2005;52:417-24.) combined were identified in our patients. Prevalence of HCV infection was 35.2%. Inherited URO-D deficiency occurs in 25.0% of cases. H63D was the most common hemochromatosis gene mutation. High incidence of PCT associated with HIV infection was found. Conclusions: PCT is multifactorial. Therefore, knowledge of all risk factors in each patient is important for the management of the disease. ( J Am Acad Dermatol 2005;52:417-24.) combined were identified in our patients. Prevalence of HCV infection was 35.2%. Inherited URO-D deficiency occurs in 25.0% of cases. H63D was the most common hemochromatosis gene mutation. High incidence of PCT associated with HIV infection was found. Conclusions: PCT is multifactorial. Therefore, knowledge of all risk factors in each patient is important for the management of the disease. ( J Am Acad Dermatol 2005;52:417-24.) combined were identified in our patients. Prevalence of HCV infection was 35.2%. Inherited URO-D deficiency occurs in 25.0% of cases. H63D was the most common hemochromatosis gene mutation. High incidence of PCT associated with HIV infection was found. Conclusions: PCT is multifactorial. Therefore, knowledge of all risk factors in each patient is important for the management of the disease. ( J Am Acad Dermatol 2005;52:417-24.) combined were identified in our patients. Prevalence of HCV infection was 35.2%. Inherited URO-D deficiency occurs in 25.0% of cases. H63D was the most common hemochromatosis gene mutation. High incidence of PCT associated with HIV infection was found. Conclusions: PCT is multifactorial. Therefore, knowledge of all risk factors in each patient is important for the management of the disease. ( J Am Acad Dermatol 2005;52:417-24.) combined were identified in our patients. Prevalence of HCV infection was 35.2%. Inherited URO-D deficiency occurs in 25.0% of cases. H63D was the most common hemochromatosis gene mutation. High incidence of PCT associated with HIV infection was found. Conclusions: PCT is multifactorial. Therefore, knowledge of all risk factors in each patient is important for the management of the disease. ( J Am Acad Dermatol 2005;52:417-24.) Several factors (mainly alcohol abuse in men and estrogen ingestion in women), alone or combined were identified in our patients. Prevalence of HCV infection was 35.2%. Inherited URO-D deficiency occurs in 25.0% of cases. H63D was the most common hemochromatosis gene mutation. High incidence of PCT associated with HIV infection was found. Conclusions: PCT is multifactorial. Therefore, knowledge of all risk factors in each patient is important for the management of the disease. ( J Am Acad Dermatol 2005;52:417-24.)Conclusions: PCT is multifactorial. Therefore, knowledge of all risk factors in each patient is important for the management of the disease. ( J Am Acad Dermatol 2005;52:417-24.)
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info:eu-repo/semantics/openAccess Excepto donde se diga explícitamente, este item se publica bajo la siguiente descripción: Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Unported (CC BY-NC-SA 2.5)
Identificadores
URI: http://hdl.handle.net/11336/147347
DOI: http://dx.doi.org/10.1016/j.jaad.2004.09.014
URL: https://www.jaad.org/article/S0190-9622(04)02489-2/fulltext
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Articulos(CIPYP)
Articulos de CENTRO DE INVEST. SOBRE PORFIRINAS Y PORFIRIAS
Citación
Méndez, Manuel; Rossetti, Maria Victoria; Batlle, Alcira María del C.; Parera, Victoria Estela; The role of inherited and acquired factors in the development of porphyria cutanea tarda in the Argentinean population; Mosby-Elsevier; Journal of the American Academy of Dermatology; 52; 3 Pt 1; 3-2005; 417-424
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