deck_5332352 Flashcards

(46 cards)

1
Q

*****What stereotypecharacterizes Chronic Bronchitis?

A

Blue Bloaters:• Overweight and Cyanotic people with Elevated Hbg (because they’re hypoxic) peripheral edema and rhonchi and wheezing.

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2
Q

*****What disease is characterized by pink puffers?• why do we call them pink puffers?

A

Emphysema = pink puffers• Older and Thin(because they burn so much energy breathing)with severe dyspnea and quiet chest sounds

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3
Q

*****Differentiate the methods of Dx for chronic bronchitis and emphysema.

A

Chronic Bronchitis:• CLINICAL dx. characterized by 3 mo. of daily productivecough for 2 consecutive yearsEmphysema:• PATHOLOGIC dx. characterized by destruction of the airspace distal to the terminal bronchioles

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4
Q

**Why would you seen an abundance of the cells pointed out by the black arrows?

A

Black arrows:•Type II pneumocytes:these are hobnail shaped and are seen in abundance following destruction oftype I pneumocytes

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5
Q

*****What are Clara Cells and what is their role in the lungs?• where are they found?

A

Clara cells =CLUB CELLS- these are dome shaped cells withshort microvillifound insmall airways (BRONCHIOLES)of the lungsROLE:PROTECTION

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6
Q

**What is being pointed out by the back arrows in this electron microscopy image?

A

Surfactant -Lamellar Bodies- that are found intype II pneumocytes

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7
Q

**What most likely accounts for the changes seen in the cells on the left and on the right?• what cells are being pointed out?

A

Left side reprsentsalveolar macrophagesin someone who is a non-smoker while the right side shows acrack cocaine usernote theincreased number of particles in the macrophages*ANY PARTICLE this is 1-5µm in size have the potential to make it to an alveolus

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8
Q

What are the 3 types of Atelectasis?• differentiate their common causes.• which way does the mediastinum shift in response?

A

3 types = Resorption, Compression, ContractionResorption:• Airway obstruciton bymucous plugsortumor,this acts as avalvethat allows air out but not back in leading to suction so the mediastium shiftstoward the affected sideCompression:•Filling of pleural cavity by tumor, blood, air,this acts tocompression of tissuepushing the mediastinumawayfrom the affected side.Contraction:•Fibrotic lung pleurathis is just a shrinking of the lung tissuethere is no mediastinal shift

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9
Q

**Which of these phenomena isirreversible?

A

Contraction- caused by fibrosis isirreversible

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10
Q

**What is happening here?

A

Resorption Atelectasis -a tumor affecting the right mainstem bronchus has resulted in markedly reduced right lung volume and rightward mediastinal shift

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11
Q

**what is happening here?

A

compressionatelectasis - left pneumothorax from chest wall trauma is resulting in left lung collapse and right mediastinal shift

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12
Q

What is the only Obstructive lung disease that is caused by loss of elastic recoil of the lung?

A

Emphysema, all of the others (chronic bronchitis, asthma, and bronchietasis) result from airway obstruction and narrowing

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13
Q

Define Emphysema?• is fibrosis typically a feature of this disease?

A

Emphysema:• Abnormalpermanentenlargement of airspaces accompanied by destruction of their walls• Fibrosis isnot a significant feature of emphysema

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14
Q

A previously healthy young adult man pressents with unknown respiratory disease developesspontaneous pneumothorax.Biopsy indicates a type of underlying obstructivedisease. What is this diseas?

A

PARASEPTALemphysema - causes pneumothorax in young adults

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15
Q

Differentiate locations and causes of centriacinar and panacinar emphysema.

A

Centriacinar:• Typically found in heavy smokers => causes XS inflammation and overactivation of proteases• Predominates in the upper lobesPanacinar:• Associated the A1AT deficiency => is not present to prevent proteases from breaking down our own tissue• Found in the lower lobes

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16
Q

*****What do you expect to see on the liver biopsy of a patient with A1AT deficiency?• what causes this appearance?• Genetics of this person?

A

Liver biopsy shows pinkPAS positive hyalineglobulesthat results from misfolded A1AT accumulating in theendoplasmic reticulum of hepatocytes - notice red blobs

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17
Q

What disease is a person with a PiMZmutation at risk of developing?• what factors would increase their risk of developing disease?

A

This is a mutant heterozygote for A1AT deficiency.• these patients areasyptomatic unless they smoke**Remember Z indicates mutation - homozygote = PiZZ => theywill have disease

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18
Q

*****T or F: Centriacinar Emphysema affects alveolar ducts only.

A

False, Respiratory bronchioles are most affected - the smoke doesn’t make it to the alveolar ducts

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19
Q

**What is wrong in this CXR?

A

Nothing - this is a normal CXR

20
Q

**What are some important characteristics to notice in this CXR?• dz?

A

Retrosternal Airspace - is not normal - heart should be close to the sterumFlattening of the Diaphragm - also not good

21
Q

**What is the most likely etiology of the lung disease shown here?

A

Emphysema - this person was most likely a smoker

22
Q

**What disease is shown here and how do you know?

A

centriacinar emphysema- central portion of acinus (where arrows are pointing) has abnormally large airspaces with club-shaped alveolar septa that appear to be floating

23
Q

**What obstructivedisease does this person most likely have/

A

Panacinar Emphysemacaused by A1AT defieciency (PiZZ) causingLOWER LOBEtissue destruction

24
Q

**What do you suspect caused this obstructivedisease?

A

A1AT - Panacinar - destruction of these alveoli is fairly uniform

25
What part of the alveoli is affected in paraseptal emphysema? 
Alveolar Ducts and Alveoli themselves 
26
**What did this person most likely die of? • Predisposing factor? 
• Shown here is a ruptured bullae that is likely the result of a ruptured bled causing pneumothroax• Paraseptal emphysema is likely the cause - happens in young adults 
27
**What pathology is seen here? • Cause? 
Paraseptal Emphysema: DISTAL airspaces show marked dilation 
28
What 4 key histologic features should you look for to see if a patient's lung biospy is consistent with Chronic Bronchitis? 
• Submucosal gland hypertrophy of large airways increased Reid Index• Increase goblet cells in smaller airways • Chronic LYMPHOCYTIC airway inflammation • Peribronchial fibrosis 
29
**What is the problem with this bronchiole? 
Mucosal Gland hypertrophy - indicative, but NOT DIAGNOSTIC of chronic bronchitisReid Index definitely exceeds 0.4 
30
**What key feature of chonic bronchitis is the red arrow pointing to? • Name the other 3 key features. 
Lymphocytic infiltrate surrounding the bronchial epithelium - notice these are plasma cells as determined by the perinuclear hof Other Features:• Increased numbers of Goblet Cells• Mucous Gland Hyperplasia • Parabronchial Fibrosis 
31
What are the 2 different types of Asthma? • differentiate between these. 
Extrinsic: • Type I (IgE) hypersensitivity reaction to inhaled allergen  Intrinsic: • Non-immunologic reaction - precipitated by respiratory tract infection, stress, exercise, cold, drugs. 
32
**What key feature of chronic bronchitis is shown here? 
• Increased goblet cells 
33
What gross features do you expect to see in a lung from a person suffering from Asthma? • Microscopic features? 
Asthma: Gross: • Overinflation and Mucous plugs  Microscopic: • Thickened Basement Membrane • Submucosal gland hypertrophy• Bronchial wall smooth muscle hypertrophy• Eosinophil-rich inflammatory infiltrate 
34
**The picture shown here is characteristic of what obstructive pulmonary disorder? • Why? 
Asthma - mucous plug in a bronchus 
35
**What 3 features should you notice in this bronchus? • what obstructive disease is this indicative of? 
3 Key Histologic Features: • Bronchial Epithelium is desquamated • Thickening of Basement membrane • Eosinophilic Inflammation 
36
**This mucous sample shows a microscopic appearance characterisitic of what COPD? 
• Charcot-Leyden crystals seen here are the result of eosinophil degradation and are seen in asthmatics 
37
**This microscopic finding is indicative of what COPD? 
• Curschmann Spirals are indicative of Asthma 
38
Histologic finding in a patient look much like asthma including eosinophilic infiltrates, but the patient's physician and medical records never indicate any history of asthma. • what should be in your differential? • What causes this disease? 
Eosinophlic Bronchitis: • these patients do not have recurrent episodes of wheezing, shortness or breath, and coughing • DO NOT respond ot BRONCHODILATORS • Cause: ideopathic or secondary to infections, drug administration or immunologic diseases 
39
What causes bronchiectasis? 
• Repeated cycles of airway OBSTRUCTION AND INFLAMMATION
40
What obstructive lung disease is associated with defective dyenin arms? 
• Bronchietasis results from obstruction and inflammation that is repeated in Kartagener's because these people have ineffective cilia and are also often infertile 
41
What 2 bugs often cause necrotizing pneumonia that can sometimes lead to bronchiectasis? 
• Staph. Aureus• Mycobacteria 
42
**What genetic mutation could lead to the disease shown here? 
• ∆F508 - Chromosome 7 - cystic fibrosis• or Dyeinin defect in Kartagener's 
43
**What is the white stuff between the bronchioles in this patient that had bronchietasis? 
FIbrosis 
44
**What is seen in this histiologic specimen? 
Bronchietasis - alveoli appear relatively normal but there is pus (neutrophils) in the airway - other than the huge fibrotic airway, the alveoli appear pretty normal 
45
*****What causes tracheoesophageal fistula? 
Failure of hte fetal respiratory tract to separate from the GI tract from which it derives. 
46
When is the saccular stage of lung development? • why is this important? 
26-32 weeks - fetal lungs develope type I and type II alveolar cells and begin making SURFACTANT