Document Detail


Type III Takayasu's arteritis in a pediatric patient. Case report and review of the literature.
MedLine Citation:
PMID:  22465417     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
Takayasu's arteritis (TA), also known as "pulseless disease", is the third most common vasculitis in childhood. It is a chronic, idiopathic, granulomatous vasculitis that involves large vessels. It occurs most commonly in females with a 4:1 ratio over males; the average age of appearance is 26 years. Its cause is unknown. Here we report the case of a 7 year old girl, with type III TA according to the Numano classification, in the ischemic phase, treated with corticosteroids and immunosuppressive agents and early angioplasty due to the severity of the disease. The outcome was satisfactory. The diagnosis of TA in children under 10 years of age is made only in 2% of them. The delay in diagnosis reaches a mean of 19 months. The course of the disease is variable despite surgical and immunosuppressive treatment.
Authors:
Karla Mendiola Ramírez; Astrid Cristina Portillo Rivera; Abraham Galicia Reyes; José Antonio García Montes; María Del Rocío Maldonado Velázquez; Enrique Faugier Fuentes
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Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-3-30
Journal Detail:
Title:  Reumatologia clinica     Volume:  -     ISSN:  1885-1398     ISO Abbreviation:  -     Publication Date:  2012 Mar 
Date Detail:
Created Date:  2012-4-2     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101293923     Medline TA:  Reumatol Clin     Country:  -    
Other Details:
Languages:  ENG; SPA     Pagination:  -     Citation Subset:  -    
Copyright Information:
Copyright © 2011 Elsevier España, S.L. All rights reserved.
Affiliation:
Servicio de Reumatología, Hospital Infantil de México Federico Gómez, México DF, México.
Vernacular Title:
Arteritis de Takayasu tipo III en un paciente pediátrico. Reporte de caso y revisión de la literatura.
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