Síndrome de hiper IgE, una enfermedad poco frecuente en edad adulta: Reporte de un caso
The Hyperimmunoglobulin E syndrome (HIES) is a rare sporadic or autosomal dominant immune and connective tissue disorder characterized by chronic eczema, cutaneous abscesses, pneumonias, invasive infections, high levels of Immunoglobulin E, primary teeth retention and bone abnormalities. We report a...
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Sociedad Médica de Santiago
2015
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oai:scielo:S0034-988720150006000142015-10-19Síndrome de hiper IgE, una enfermedad poco frecuente en edad adulta: Reporte de un casoAguilera S,GuillermoCárcamo R,GuillermoSepúlveda E,JuanVinet R,Ana MaríaMartínez H,Carlos Cryoglobulinemia Hyper-IgE Syndrome Job Syndrome The Hyperimmunoglobulin E syndrome (HIES) is a rare sporadic or autosomal dominant immune and connective tissue disorder characterized by chronic eczema, cutaneous abscesses, pneumonias, invasive infections, high levels of Immunoglobulin E, primary teeth retention and bone abnormalities. We report a 24-year-old male with a history of cutaneous abscesses and esophageal candidiasis. He was admitted due to a left gluteal cellulitis. During the fifth day of hospitalization he presented a distal necrosis of the fourth finger of the right hand. Laboratory results showed high levels of IgE and positive cryoglobulins. The patient was discharged and was admitted again five days later with a new gluteal abscess. IgE levels were even higher. Applying Grimbacher scale, the diagnosis of Hyperimmunoglobulin E syndrome was reached.info:eu-repo/semantics/openAccessSociedad Médica de SantiagoRevista médica de Chile v.143 n.6 20152015-06-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872015000600014es10.4067/S0034-98872015000600014 |
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Scielo Chile |
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Scielo Chile |
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Spanish / Castilian |
topic |
Cryoglobulinemia Hyper-IgE Syndrome Job Syndrome |
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Cryoglobulinemia Hyper-IgE Syndrome Job Syndrome Aguilera S,Guillermo Cárcamo R,Guillermo Sepúlveda E,Juan Vinet R,Ana María Martínez H,Carlos Síndrome de hiper IgE, una enfermedad poco frecuente en edad adulta: Reporte de un caso |
description |
The Hyperimmunoglobulin E syndrome (HIES) is a rare sporadic or autosomal dominant immune and connective tissue disorder characterized by chronic eczema, cutaneous abscesses, pneumonias, invasive infections, high levels of Immunoglobulin E, primary teeth retention and bone abnormalities. We report a 24-year-old male with a history of cutaneous abscesses and esophageal candidiasis. He was admitted due to a left gluteal cellulitis. During the fifth day of hospitalization he presented a distal necrosis of the fourth finger of the right hand. Laboratory results showed high levels of IgE and positive cryoglobulins. The patient was discharged and was admitted again five days later with a new gluteal abscess. IgE levels were even higher. Applying Grimbacher scale, the diagnosis of Hyperimmunoglobulin E syndrome was reached. |
author |
Aguilera S,Guillermo Cárcamo R,Guillermo Sepúlveda E,Juan Vinet R,Ana María Martínez H,Carlos |
author_facet |
Aguilera S,Guillermo Cárcamo R,Guillermo Sepúlveda E,Juan Vinet R,Ana María Martínez H,Carlos |
author_sort |
Aguilera S,Guillermo |
title |
Síndrome de hiper IgE, una enfermedad poco frecuente en edad adulta: Reporte de un caso |
title_short |
Síndrome de hiper IgE, una enfermedad poco frecuente en edad adulta: Reporte de un caso |
title_full |
Síndrome de hiper IgE, una enfermedad poco frecuente en edad adulta: Reporte de un caso |
title_fullStr |
Síndrome de hiper IgE, una enfermedad poco frecuente en edad adulta: Reporte de un caso |
title_full_unstemmed |
Síndrome de hiper IgE, una enfermedad poco frecuente en edad adulta: Reporte de un caso |
title_sort |
síndrome de hiper ige, una enfermedad poco frecuente en edad adulta: reporte de un caso |
publisher |
Sociedad Médica de Santiago |
publishDate |
2015 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872015000600014 |
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