Microlitiasis alveolar pulmonar: caso clínico
Pulmonary alveolar microlithiasis is an extremely rare disease characterized by intra-alveolar accumulation of calcified spherical particles (called microliths), due to a mutation of the gene encoding a membrane transport protein of the alveolar surface. Most patients are asymptomatic at diagnosis....
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Sociedad Médica de Santiago
2014
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oai:scielo:S0034-988720140005000162014-10-10Microlitiasis alveolar pulmonar: caso clínicoFernández F,CristinaSalinas F,Mauriciode Grazia K,José AndrésDíaz P,Juan Carlos Lung diseases Pulmonary alveolar microlithiasis Tomography scanners X-Ray computed Pulmonary alveolar microlithiasis is an extremely rare disease characterized by intra-alveolar accumulation of calcified spherical particles (called microliths), due to a mutation of the gene encoding a membrane transport protein of the alveolar surface. Most patients are asymptomatic at diagnosis. The course of the disease is slowly progressive, with development of pulmonary fibrosis and respiratory failure. The "sandstorm" pattern is the characteristic finding of this disease. We report a 39-year-old female presenting with progressive dyspnea. A chest X ray showed ground-glass opacities and a high resolution CT scan showed numerous calcified lung micronodules. A surgical lung biopsy confirmed the diagnosis of pulmonary alveolar microlithiasis.info:eu-repo/semantics/openAccessSociedad Médica de SantiagoRevista médica de Chile v.142 n.5 20142014-05-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872014000500016es10.4067/S0034-98872014000500016 |
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Scielo Chile |
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Scielo Chile |
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Spanish / Castilian |
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Lung diseases Pulmonary alveolar microlithiasis Tomography scanners X-Ray computed |
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Lung diseases Pulmonary alveolar microlithiasis Tomography scanners X-Ray computed Fernández F,Cristina Salinas F,Mauricio de Grazia K,José Andrés Díaz P,Juan Carlos Microlitiasis alveolar pulmonar: caso clínico |
description |
Pulmonary alveolar microlithiasis is an extremely rare disease characterized by intra-alveolar accumulation of calcified spherical particles (called microliths), due to a mutation of the gene encoding a membrane transport protein of the alveolar surface. Most patients are asymptomatic at diagnosis. The course of the disease is slowly progressive, with development of pulmonary fibrosis and respiratory failure. The "sandstorm" pattern is the characteristic finding of this disease. We report a 39-year-old female presenting with progressive dyspnea. A chest X ray showed ground-glass opacities and a high resolution CT scan showed numerous calcified lung micronodules. A surgical lung biopsy confirmed the diagnosis of pulmonary alveolar microlithiasis. |
author |
Fernández F,Cristina Salinas F,Mauricio de Grazia K,José Andrés Díaz P,Juan Carlos |
author_facet |
Fernández F,Cristina Salinas F,Mauricio de Grazia K,José Andrés Díaz P,Juan Carlos |
author_sort |
Fernández F,Cristina |
title |
Microlitiasis alveolar pulmonar: caso clínico |
title_short |
Microlitiasis alveolar pulmonar: caso clínico |
title_full |
Microlitiasis alveolar pulmonar: caso clínico |
title_fullStr |
Microlitiasis alveolar pulmonar: caso clínico |
title_full_unstemmed |
Microlitiasis alveolar pulmonar: caso clínico |
title_sort |
microlitiasis alveolar pulmonar: caso clínico |
publisher |
Sociedad Médica de Santiago |
publishDate |
2014 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872014000500016 |
work_keys_str_mv |
AT fernandezfcristina microlitiasisalveolarpulmonarcasoclinico AT salinasfmauricio microlitiasisalveolarpulmonarcasoclinico AT degraziakjoseandres microlitiasisalveolarpulmonarcasoclinico AT diazpjuancarlos microlitiasisalveolarpulmonarcasoclinico |
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1718436757169504256 |