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http://scihub22266oqcxt.onion/ 33906153!?!33906153 Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=33906153&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215       Medicina+(B+Aires) 2021 ; 81 (2): 301-303 Nephropedia Template TP {{tp|p=33906153|t=2021. Proteinosis alveolar pulmonar |pdf=|usr=}}{{33906153}} gab.com Text Proteinosis alveolar pulmonar JO: Medicina (B Aires) http://www.kidney.de/pget.php?&tw=1&pmid=33906153 #FOAvip Pulmonary alveolar proteinosis (PAP) is a rare, diffuse pulmonary disease due to abnormal surfactant homeostasis. We present the case of a 69-year-old woman who was admitted to the hospital for progressive dyspnea with marked limitation in activity, and non-productive cough, of three months of evolution. Type I respiratory failure was confirmed. Chest tomography findings were interlobular and intralobular septal thickening, ground glass opacities and bilateral consolidation. Histological diagnosis was made and whole-lung lavage was performed with clinical improvement. We highlight the need to keep in mind differential diagnoses of respiratory failure and pulmonary infiltrates during COVID-19 pandemic, even rare entities such as PAP. Twit Text FOAVip Proteinosis alveolar pulmonar ????Medicina (B Aires) http://www.kidney.de/pget.php?&tw=1&pmid=33906153 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=33906153 #FOAvip English Wikipedia <ref>{{Cite pmid|33906153}}</ref> Proteinosis alveolar pulmonar #MMPMID33906153 Pensa LA; Solerno MR; Rausch S; Aruj PK; Grinberg AR Medicina (B Aires) 2021[]; 81 (2): 301-303 PMID33906153show ga Pulmonary alveolar proteinosis (PAP) is a rare, diffuse pulmonary disease due to abnormal surfactant homeostasis. We present the case of a 69-year-old woman who was admitted to the hospital for progressive dyspnea with marked limitation in activity, and non-productive cough, of three months of evolution. Type I respiratory failure was confirmed. Chest tomography findings were interlobular and intralobular septal thickening, ground glass opacities and bilateral consolidation. Histological diagnosis was made and whole-lung lavage was performed with clinical improvement. We highlight the need to keep in mind differential diagnoses of respiratory failure and pulmonary infiltrates during COVID-19 pandemic, even rare entities such as PAP. |*COVID-19[MESH] |*Pulmonary Alveolar Proteinosis/diagnostic imaging/therapy[MESH] |Aged[MESH] |Female[MESH] |Humans[MESH] |Lung[MESH] |Pandemics[MESH]Proteinosis alveolar pulmonar (epmc).pdf DeepDyve Pubget Overpricing