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array:19 [ "pii" => "13046510" "issn" => "15792129" "estado" => "S300" "fechaPublicacion" => "2003-07-01" "documento" => "article" "crossmark" => 0 "subdocumento" => "fla" "cita" => "Arch Bronconeumol. 2003;39:327" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 2452 "formatos" => array:3 [ "EPUB" => 108 "HTML" => 1770 "PDF" => 574 ] ] "itemSiguiente" => array:15 [ "pii" => "13046512" "issn" => "15792129" "estado" => "S300" "fechaPublicacion" => "2003-07-01" "documento" => "article" "crossmark" => 0 "subdocumento" => "fla" "cita" => "Arch Bronconeumol. 2003;39:328" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 2053 "formatos" => array:3 [ "EPUB" => 114 "HTML" => 1400 "PDF" => 539 ] ] "en" => array:9 [ "idiomaDefecto" => true "titulo" => "Authors¿ reply" "tienePdf" => "en" "tieneTextoCompleto" => "en" "paginas" => array:1 [ 0 => array:1 [ "paginaInicial" => "328" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Respuesta de los autores" ] ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "N Salord, R M Miralda, P Casan" "autores" => array:3 [ 0 => array:2 [ "Iniciales" => "N" "apellidos" => "Salord" ] 1 => array:2 [ "Iniciales" => "R M" "apellidos" => "Miralda" ] 2 => array:2 [ "Iniciales" => "P" "apellidos" => "Casan" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/13046512?idApp=UINPBA00003Z" "url" => "/15792129/0000003900000007/v0_201307090915/13046512/v0_201307090915/en/main.assets" ] "itemAnterior" => array:15 [ "pii" => "13046511" "issn" => "15792129" "estado" => "S300" "fechaPublicacion" => "2003-07-01" "documento" => "article" "crossmark" => 0 "subdocumento" => "fla" "cita" => "Arch Bronconeumol. 2003;39:327-8" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 5468 "formatos" => array:3 [ "EPUB" => 106 "HTML" => 4773 "PDF" => 589 ] ] "en" => array:9 [ "idiomaDefecto" => true "titulo" => "The progression of amyotrophic lateral sclerosis (ALS): respiratory function" "tienePdf" => "en" "tieneTextoCompleto" => "en" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "327" "paginaFinal" => "328" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Evolución de la esclerosis lateral amiotrófica a través de la función pulmonar" ] ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "S Mayoralas, M A Gómez, S Díaz" "autores" => array:3 [ 0 => array:2 [ "Iniciales" => "S" "apellidos" => "Mayoralas" ] 1 => array:2 [ "Iniciales" => "M A" "apellidos" => "Gómez" ] 2 => array:2 [ "Iniciales" => "S" "apellidos" => "Díaz" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/13046511?idApp=UINPBA00003Z" "url" => "/15792129/0000003900000007/v0_201307090915/13046511/v0_201307090915/en/main.assets" ] "en" => array:10 [ "idiomaDefecto" => true "titulo" => "Alveolar proteinosis or the importance of identifying concurrent infections" "tieneTextoCompleto" => true "paginas" => array:1 [ 0 => array:1 [ "paginaInicial" => "327" ] ] "autores" => array:1 [ 0 => array:3 [ "autoresLista" => "S Mayoralas, L Gómez, S Díaz" "autores" => array:3 [ 0 => array:3 [ "Iniciales" => "S" "apellidos" => "Mayoralas" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] 1 => array:3 [ "Iniciales" => "L" "apellidos" => "Gómez" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] 2 => array:3 [ "Iniciales" => "S" "apellidos" => "Díaz" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] ] "afiliaciones" => array:1 [ 0 => array:3 [ "entidad" => "Servicio de Neumología. Hospital Universitario La Paz. Madrid. Spain." "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Proteinosis alveolar o la importancia de identificar infecciones sobreañadidas" ] ] "textoCompleto" => "<p class="elsevierStylePara"><span class="elsevierStyleBold"> To the Editor:</span> Alveolar proteinosis (AP) is a rare disease which affects the lungs diffusely and is characterized by the deposition of protein-like material rich in phospholipids. This material is characteristically PAS positive and does not cause interstitial alveolar inflammation; thus the degree of fibrosis minimal<span class="elsevierStyleSup">1</span>. Signs and symptoms are nonspecific and patients are generally asymptomatic before complications occur. The main complication in AP is concurrent infection with unusual germs like <span class="elsevierStyleItalic">Aspergillus</span> sp.<span class="elsevierStyleItalic">, Nocardia</span> sp.<span class="elsevierStyleItalic">, Mycobacterium</span> sp.<span class="elsevierStyleItalic">, Cryptococcus neoformans, Histoplasma capsulatum, Pneumocystis carinii</span> and certain viruses<span class="elsevierStyleSup">2</span>. We report the case of a woman diagnosed with AP after being infected with <span class="elsevierStyleItalic">Mycobacterium tuberculosis</span>.</p><p class="elsevierStylePara">The patient was a 41-year-old female who smoked 500 cigarettes per year and was a moderate drinker with no relevant medical or occupational history. The patient complained of night sweats, dyspnea upon moderate effort, cough with abundant whitish sputum and wasting syndrome with loss of 6 to 7 kg in weight starting three months earlier. She had presented bloody sputum on one occasion one week before admission. Perihilar ground-glass opacities were observed in the chest radiograph. Physical exploration showed no significant findings. Relevant analytical findings were leukocytes, 6550/µl (neutrophiles 57%, lymphocytes 34%); hemoglobin, 14 g/dL; hematocrit, 38.6%; platelets, 212 000; and erythrocyte sedimentation rate, 10 mm/h. Biochemistry, proteinogram, coagulation and urine analyses were normal. Nuclear antibodies, anti-smooth muscle and rheumatoid factors were normal. The angiotensin-converting enzyme level was 51 (30-50). The pneumonia panel was negative and no <span class="elsevierStyleItalic">Legionella</span> antigen was found in urine. Lung function testing gave normal findings, including a carbon monoxide diffusion capacity of 82.3%. Resting arterial gases were measured, pH being 7.39, PaO<span class="elsevierStyleInf">2</span> 68 mmHg and PaCO<span class="elsevierStyleInf">2</span> 41 mmHg. A computed tomography scan of the thorax showed bilateral ground-glass opacities, mainly in high and mid fields. Bronchoscopy revealed no endobronchial lesions, but PAS-positive material was detected in bronchial aspirate and bronchoalveolar lavage samples. The Löwenstein­Jensen culture was positive for <span class="elsevierStyleItalic">M. tuberculosis</span>. A transbronchial biopsy gave no remarkable findings. There was good response to treatment with isoniazid and rifampicin for six months and with pyrazinamide for the first two months. The patient remained asymptomatic one year later. A chest radiograph showed no changes, pulmonary function tests were normal and the biopsy was still PAS positive. Löwenstein-Jensen cultures were negative.</p><p class="elsevierStylePara">The clinical presentation of AP is variable and nonspecific. The most frequent symptoms are dry cough and dyspnea. Some patients present no symptoms before developing concurrent infections, as in the case we report. Although favorable results have been described after treatment with granulocytic-monocytic series colony stimulating factor<span class="elsevierStyleSup">3</span>, the only treatment of proven efficacy is whole-lung lavage<span class="elsevierStyleSup">4</span>. This treatment is only prescribed for patients with dyspnea or respiratory insufficency<span class="elsevierStyleSup">5,6</span>. Nevertheless, before considering whole-lung lavage, it is necessary to rule out specifically treatable concurrent infections. Our patient experienced symptoms while the <span class="elsevierStyleItalic">M. tuberculosis</span> infection persisted and remained asymptomatic after being treated; therefore, whole-lung lavage was not considered. With the exception of patients with severe respiratory insufficiency, identifying and treating concurrent infections is the best way to improve quality of life and prognosis for AP patients. While these infections were the main cause of death in the past, the prognosis has currently improved considerably with their appropriate treatment.</p>" "pdfFichero" => "260v39n07a13046510pdf001.pdf" "tienePdf" => true "bibliografia" => array:2 [ "titulo" => "Bibliography" "seccion" => array:1 [ 0 => array:1 [ "bibliografiaReferencia" => array:6 [ 0 => array:3 [ "identificador" => "bib1" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:3 [ "titulo" => "Update on the clinical diagnosis, management and pathogenesis of pulmonary alveolar proteinosis." 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"idioma" => "en" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:4 [ 0 => "Bingisser R" 1 => "Kaplan V" 2 => "Zollinger A" 3 => "Russi EW." ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ "tituloSerie" => "Chest" "fecha" => "1998" "volumen" => "113" "paginaInicial" => "1718" "paginaFinal" => "9" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/9631820" "web" => "Medline" ] ] ] ] ] ] ] ] 4 => array:3 [ "identificador" => "bib5" "etiqueta" => "5" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:3 [ "titulo" => "Pulmonary alveolar proteinosis causing severe hypoxemic respiratory failure treated with sequential whole-lung lavage utilizing venovenous extracorporeal membrane oxygenation: a case report and review." 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