A novel immunodeficiency syndrome as a rare cause of secondary pulmonary alveolar proteinosis: A diagnosis after 5 decades

Revista Portuguesa de Pneumologia

Volumn 20, Issue 5, 2014, Pages 273-278

  Ferreira, Pedro G ^a   Carvalho, Lina ^a   Gamboa, Fernanda ^a  

^a CENTRO HOSPITALAR E UNIVERSITÁRIO DE COIMBRA   (Portugal)

Author keywords

Alveolar pulmonary proteinosis; Immunodeficiency; Parenchymal lung disease; Systemic disease with lung involvement

Indexed keywords

TRANSCRIPTION FACTOR GATA 2; TUBERCULOSTATIC AGENT;

ADULT; ARTICLE; B LYMPHOCYTE; BONE MARROW BIOPSY; BRONCHOSCOPY; CASE REPORT; COMPUTER ASSISTED TOMOGRAPHY; DENDRITIC CELL; EPIDERMODYSPLASIA VERRUCIFORMIS; FAILURE TO THRIVE; FLOW CYTOMETRY; GENE MUTATION; HUMAN; HUMAN TISSUE; IMMUNE DEFICIENCY; LUNG ALVEOLUS PROTEINOSIS; LUNG BIOPSY; LUNG TUBERCULOSIS; MALABSORPTION; MALE; MENINGITIS; MIDDLE AGED; MONOCYTE; MONOCYTOPENIA; NATURAL KILLER CELL; PNEUMOCOCCAL MENINGITIS; COMPLICATION; IMMUNOLOGIC DEFICIENCY SYNDROMES; PULMONARY ALVEOLAR PROTEINOSIS; TIME;

B-LYMPHOCYTES; DENDRITIC CELLS; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; KILLER CELLS, NATURAL; MALE; MIDDLE AGED; MONOCYTES; PULMONARY ALVEOLAR PROTEINOSIS; TIME FACTORS;

EID: 84906789708     PISSN: 08732159     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.rppneu.2013.08.006     Document Type: Article

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