lung julia Flashcards
Tracheoesophageal (TE) Fistula
congential
- abnormal connection between the trachea and esophagus
- associated with esophageal atresia (absence or closure of a portion of the esophagus)
classic lobar PNA: what bacteria and stages
associated with streptococcus
4 stages:
- congestion
- red hepatization: red lung with exudation - neutrophils, red cells, fibrin in alveolar space
- gray hepatization: disintegrated red cells but persistence of fibrinosuppurative exudate
- resolution: exudates broken down to produce granular semifluid debris that is resorbed by macrophages or organized by fibrobalsts
Atelectasis: and types
Atelectasis – incomplete expansion of lung, or collapse
Resorption atelectasis – usually cause be obstruction, e.g tumor
Compression atelectasis – pleural fluid compresses lung
Contraction atelectasis – assoc. with diffuse fibrotic lung diseases
ARDS: Acute Respiratory Distress Syndrome
ARDS (Acute Respiratory Distress Syndrome) = non-specific pattern of lung injury –> alveoli lined by hyaline membranes so no oxygen exchange can take place
= “end-stage” lung
- Multiple causes-
- diffuse alveolar damage
Pulmonary edema
INC venous P + DEC oncotic P + lymphatic obstruction + alveolar injury
Chronic Obstructive Lung Disease: emphysema, types
Emphysema – destruction of alveolar walls causing enlargement of air spaces
- progressive air trapping and can cause recurrent PNA
Centriacinar emphysema: Cigarette smoking
Panacinar emphysema: alpha-1-antitrypsin deficiency
emphysema xray findings
Hyperexpansion
flattened/blunted diaphragm
increased lucency
heart may appear narrow
Bullae/blebs
Chronic Bronchitis
main cause usually smoking
- mucus hypersecretion due to GOBLET cell hyperplasia
- chronic inflammation -> can progress to emphysema
Asthma: histological findings
Histological findings in bronchi(oles)
- mucus hypersecretion with plugging
- Eosinophils/lymphocytes
- lumen narrowing
- smooth muscle hypertrophy around bronchi & bronchioles: constant spasms = hyperplasia
wheezing is characteristic!!!**
Atopic (allergic) vs Non-atopic:
- strong allergic role: IgE, eosinophils
Restrictive Lung Diseases
Density of lung is increased, less “spongy,” dec compliance
- cant inhale
- reduced gas exchange: anatomic or functional barriers between the endothelial cells of capillaries and type-1 pneumocytes (gas exchange cells) in the alveoli.
types:
- fibrosing
- granulomatous
- eosinophilic
- smoking related
- PAP: pulmonary alveolar proteinosis
Bronchiectasis
Bronchiectasis = dilated bronchus
- associated with chronic necrotizing inflammation
- congenital, TB, bronchial obstruction, RA, SLE, IBD
- condition where large bronchi damaged and dilated
Fibrosing Restrictive Lung Diseases types
idiopathic pulmonary fibrosis
- typical histology: usual interstitial pneumonia with areas of young and old fibrosis scattered together through lung
- injured epithelial cells may produce TGF-beta which is fibrinogenic
non-specific interstitial pneumonia:
- fibrosis and cellular infiltration but better diagnosis
other associations: collagen vascular diseases
- RA
- SLE (lupus)
- systemic sclerosis
Pneumoconioses/Occupational lung diseases
articles 1 – 5 um most dangerous - coal, silica, asbestos
- Macrophages ingest them –> stimulate immune system
- Over 5: cilia can push it out; under 1 - macrophages can push it out
types: coal workers pneumoconiosis, asbestos-related lung disease, silica
Granulomatous restrictive lung ds
Sarcoidosis
- systemic but usually involves lung
- immune, genetic factors
–> non-caseating (non-necrotizing) granulomatous inflammation [some with Schaumann bodies and asteroid bodies]
Hypersensitivity pneumonitis :
- Granulomatous reaction to inhaled organic antigens -> interstitial fibrosis
- dusts, bacteria, fungi, Farmer’s Lung, Pigeon Breeder’s Lung = immune mediated-reaction to inhaled organic dusts
- 2/3 pts: non-caseating granulomas
- When removed from source, patient improves but then recurs upon re-exposure
DIP = desquamative interstitial pneumonia
- = presence of alveolar macrophages with pigment
- smoking related restrictive lung disease
pulmonary alveolar proteinosis
restrictive lung ds
caused by
- deficiency in GM-CSF
- macrophage dysfunction
- accumulation of intra-alveolar precipitates containing surfactant
- 90% autoimmune
Pulmonary Vascular Diseases : Pulmonary embolism
-may be secondary to immobilization, debilitative states
- thrombi usually come from deep leg veins or deep pelvic veins
Key Features for dx:
- acute chest pain, decreased pO2
- VQ scan shows ventilation-perfusion mismatch *
- angiogram important *
CAP: acute bacterial what PNA presentation
COVID-19 – coronavirus
can range from asymptomatic to ARDS to death
- many different signs and symptoms
- main sx: fatigue, fever, cough, SOB
pathology:
- virus attaches to ACE2 receptor especially present in lungs but also present in other tissues such as heart, cardiac manifestations, coagulopathies, and many others associated with virus
CT: “ground glass” opacities *
Lung Tumors: general characteristics and development sequence
- 90% are carcinomas (not sarcomas)
- very associated with tobacco smoking but also associated with radiation, asbestos, and radon
- Lung is the MC site for metastatic tumors (sarcomas)
Sequence of development
- normal mucosa –> metaplastic –> dysplastic –> carcinoma-in-situ (squamous, adeno) –> invasive/infiltrating cancer
pleural effusion: types
Hydrothorax - transudate vs exudate
- exudative = pus
Hemothorax
Chylothorax (lymph)
