Number of the records: 1
fibróza pľúcna idiopatická
SYS d054990 LBL 00000cz--a2200000n--4500 005 20250606214903.2 008 080101|||anznnbabn-----------|-a|a------ 040 $b slo $a BA006 $d BA006 065 $a C08.381.483.652.500 066 $a 01 $c 03 150 $a fibróza pľúcna idiopatická $x BL $x CF $x CI $x CL $x CN $x CO $x DG $x DH $x DI $x DT $x EC $x EH $x EM $x EN $x EP $x ET $x GE $x HI $x IM $x ME $x MI $x MO $x NU $x PA $x PC $x PP $x PS $x PX $x RH $x RT $x SU $x TH $x UR $x VE $x VI $2 slo 450 $w v $a Cryptogenic Fibrosing Alveolitis $2 eng 450 $w v $a alveolitída fibrozujúca kryptogénna $2 slo 665 $a 2009 $2 eng 665 $a Pulmonary Fibrosis (1964-2008) $2 eng 680 9-
$i A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change. $2 eng 680 $a PULMONARY FIBROSIS is also available $2 eng 750 -2
$a Idiopathic Pulmonary Fibrosis $2 eng 980 $x M
Number of the records: 1