My 57 year old husband, smoker for 30 years was just diagnosed with stage 1 emphysema and pulmonary
fibrosisCystic fibrosis
Cystic fibrosis - resources
Neonatal cystic fibrosis screening. CT w/ IV contrast came back w/ impressions:
1. Hyperinflation w/ peripheral/subpleural
interstitialInterstitial cystitis (ic)
Interstitial cystitis - resources
Interstitial nephritis scarring in both lungs, w/ widely scattered small parenchymal blebs, greater on the right side. Peripheral honeycombing w/in the superior segment of the R lower lobe. Findings would raise ? of underlying
idiopathicBell's palsy
Fibrous dysplasia
Guillain-barre syndrome
Hypertrophic cardiomyopathy
Idiopathic aplastic anemia
Juvenile rheumatoid arthritis
Orbital pseudotumor
Pseudotumor cerebri pulmonary
fibrosisCystic fibrosis
Cystic fibrosis - resources
Neonatal cystic fibrosis screening.
2.
FocalFocal neurological deficits area of atelectasis occupies the
posteriorAnterior vaginal wall repair
Posterior fossa tumor
Posterior heart arteries
Posterior spinal anatomy
Skeleton (posterior view)
Spinal fusion
Uveitis
Vertebrobasilar circulatory disorders aspect of the R lower lung zone but no acute infiltration or other suspicious intrapulmonary lesion.
3. Scattered hepatic cysts measure up to approx 1.3 X 0.9 cm in size. Tiny cortical cyst of the lateral aspect mid pole right kidney.
What does all this mean? Dr. took additional blood work but don't have results till this Fri. Everything I've read points to a very poor prognosis, less than 5 year survival rate for PF alone, not including emphysema diagnosis too. Does honeycomb findings indicate late stage PF? What specific questions can I ask his Dr. so we can better understand what lies ahead for him? Please help. Thanks.