Artritis séptica en un caso de síndrome de hiperinmunoglobulinemia E.

Saved in:
Bibliographic Details
Title: Artritis séptica en un caso de síndrome de hiperinmunoglobulinemia E.
Alternate Title: Septic arthritis in a case of hyper-IgE syndrome.
Authors: Fernández, Inmacu;lada Macías1
Source: Reumatología Clínica. ene/feb2010, Vol. 6 Issue 1, p53-55. 3p.
Subjects: ARTHRITIS, IMMUNOGLOBULIN E, SKIN infections, SKIN inflammation, EOSINOPHILIA, SKIN care, SCOLIOSIS
Abstract (English): Hyper-IgE syndrome (HIES) is characterized by recurrent skin and pulmonary infections (mainly bacterial), eczematous dermatitis and elevated serum lgE levels. Associated abnormalities in some patients include coarse facial features, failure or delay of shedding of primary teeth, recurrent fractures, hyperextensible joints, and scoliosis. Laboratory abnormalities include elevated total serum IgE levels, typically ranging from 1000 to greater than 50,000 IU/mL and variable eosinophilia. The diagnosis of HIES is based upon the presence of suggestive clinical and laboratory findings. A definitive laboratory test is not commercially available at present, Management of patients with HIES is focused on skin care. prevention of infection. prompt and complete treatment of infections that do develop, and control of pulmonary complications. [ABSTRACT FROM AUTHOR]
Abstract (Spanish): El síndrome de híperinmunoglobulinemia E (HIES) se caracteriza por infecciones recurrentes cutáneas y pulmonares (principalmente bacterianas), dermatitis eccematosa y elevados niveles séricos de IgE. Anomalías asociadas en algunos pacientes incluyen rasgos faciales toscos, fracaso o retraso de la caída de los dientes primarios, fracturas recurrentes, hiperlaxitud en las articulaciones y escoliosis. Anormalidades de laboratorio son niveles elevados de IgE total en suero, generalmente, de 1.000 a más de 50.000U/ml y eosinofilia variable. El diagnóstico de HIES se basa en la presencia de característicos hallazgos clínicos y de laboratorio. Un test diagnóstico definitivo no existe en la actualidad. Él manejo de los pacientes con HIES se centra en el cuidado de la piel, la prevención de la infección, el tratamiento precoz de las infecciones que se desarrollan y el control de las complicaciones pulmonares. [ABSTRACT FROM AUTHOR]
Copyright of Reumatología Clínica is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: MedicLatina
Description
Abstract:Hyper-IgE syndrome (HIES) is characterized by recurrent skin and pulmonary infections (mainly bacterial), eczematous dermatitis and elevated serum lgE levels. Associated abnormalities in some patients include coarse facial features, failure or delay of shedding of primary teeth, recurrent fractures, hyperextensible joints, and scoliosis. Laboratory abnormalities include elevated total serum IgE levels, typically ranging from 1000 to greater than 50,000 IU/mL and variable eosinophilia. The diagnosis of HIES is based upon the presence of suggestive clinical and laboratory findings. A definitive laboratory test is not commercially available at present, Management of patients with HIES is focused on skin care. prevention of infection. prompt and complete treatment of infections that do develop, and control of pulmonary complications. [ABSTRACT FROM AUTHOR]
ISSN:1699258X
DOI:10.1016/j.reuma.2009.01.011