Pathology Flashcards

1
Q

Lining Epithelium of respiratory system ?

A

Pseudostratified, ciliated columnar epithelium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Vocal cords lining epithelium ?

A

Stratified squamous

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Cells of alveoli with functions ?

A

Type 1 pneumocytes (95%) : flat cells
Type 2 : globular, surfactant, promotes healing

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Define emphysema?

A

Irreversible
Distal to terminal epithelium ( acinus )

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Fibrosis in emphysema ?

A

No

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Pathogenesis of emphysema?

A

Smoking/A1AT deficiency
Increased elastase activity
Destruction Of lung architecture

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Types of emphysema

A

Centrilobular/centriacinar
Panacinar
Paraseptal/distal
Irregular

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Emphysema associated with spontaneous pneumothorax?

A

Paraseptal/distal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Tell locations of emphysemas ?

A

Upper lobe : centriacinar
Lower lobe : panacinar

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Type of inheritance in A1ATD?

A

AR(ch.14)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

A1ATD clinical features?

A

Lungs: panacinar emphysema
Liver : cirrhosis (pas+)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Normal vs diseases A1ATD?

A

PiMM : N
PiZZ : diseases

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Floating septa seen in ?

A

Emphysema(broken alveolar wall )

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

C/f of emphysema?

A

Pink puffers
Barrel chest
Pursed lip breathing
Flattened diaphragm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Define chronic bronchitis?

A

Persistent productive cough for at least 3 consecutive months for 2 consecutive years

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Pathogenesis of chronic bronchitis?

A

Smoking
Mucosal irritations
Increased mucus
Increased reid index
Productive cough
Increased infections

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Reid index normal value and in CB?

A

Normal : 0.4
Increased in chronic bronchitis
Normal in asthma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Blue bloaters and cough : dx?

A

Chronic bronchitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Bronchial asthma genes, cytokines,cells,HSRx,earliest mediator?

A

Type 1 HS
Cells: mast and eosinophils
Cytokines IL4,IL5
Earliest mediator: histamine
Genes for atopy: ch 5
Genes : IL13,ADAM33

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Sputum of asthma ?

A

3Cs :
Curshman spirals (whorled mucus plugs)
Creola bodies
Charcoat leyden crystals (eosinophils) galectin 10

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Sputum of asthma ?

A

3Cs :
Curshman spirals (whorled mucus plugs)
Creola bodies
Charcoat leyden crystals (eosinophils) galectin 10

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Airway changes in asthma ?

A

Increased thickness
Eosinophils & mast cells in lamina propria
Smooth muscle hyperplasia
Submucosal gland hyperplasia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Etiology of bronchiectasis?

A

Congenital : kartagener & CF
Aquired : foreing body, tumours, infections

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Triad of kartagener syndrome ?

A

Situs inversus
Bronchiectasis
Sinusitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Defect in kartagener syndrome ?
Dyeinin arm of cilia
26
C/f of immotile cilia syndrome ?
B/L lower lobes Productive cough Dyspnea
27
Complications of primary cilia dyskinesia?
Sepsis Empyema Lung abscess Brain abscess Amyloidosis(AA)
28
Gross finding of bronchiectasis?
Probe reaches pleura
29
Which pneumoconiosis affects upper lobe & lower lobes?
CWP & Silicosis : upper lobes Asbestosis : lower lones
30
Pneumoconiosis risk factors?
Particles size Particle solubility Duration Synergistic factors (smoking)
31
Most pathogenic risk factors for pneumoconiosis?
0-5 micron size
32
Caplan syndrome?
CWP/Silicosis + Rheumatoid arthritis
33
C/f of CWP?
Asymptomatic anthracosis Simple CWP (coal macule,coal nodule) Progressive massive fibrosis
34
Most common pneumoconiosis?
Silicosis = grinder disease
35
Egg shell calcification seen in
Silicosis on CXR due to LN enlargement
36
Silicosis associated with increased risk of
TB Lung cancer
37
Histopathology of silicosis?
Whorled collagen bundles
38
Gross of silicosis?
Silicotic nodule Collagenous scar
39
Polarized microscopy of silicosis?
Birefringent silical particle
40
Asbestosis found in which industry workers ?
Shipping , construction
41
Asbestos fibres?
Serpentine Amphibole
42
More carcinogenic asbestos fibre?
Amphibole
43
Most common presentation of asbestosis?
Pleural plaque
44
Most common malignancy in asbestosis?
Lung adenocarcinoma
45
Most specific carcinoma for asbestosis.
Malignant mesothelioma
46
Ferruginous body seen in ?
Asbestosis It is coated with iron Dumbell shaped , beaded, fusiform, rod like
47
Stain for asbestosis body ?
Prussian blue
48
What is psammoma body ?
Foci of dystrophic calcification Basophilic
49
Psammoma bodies seen in
Papillary carcinoma of thyroid Prolactinoma Serous cystadenoma of ovary Mesothelioma Meningioma
50
Berryliosis type of granuloma ?
Non caseating
51
Baritosis, byssinosis, bagassosis, siderosis?
Barium toxicity Cotton Sugarcane Irom
52
Honeycomb lung seen in ?
Fibrosing restrictive lung diseases
53
Masson bodies seen in ?
BOOP
54
Idiopathic pulmonary fibrosis other name and mutation?
UIP TERT/TERC mutation
55
Pulmonary alveolar proteinosis?
Defect in surfactant
56
Types of pulmonary alveolar proteinosis?
Congenital Autoimmune (more common )
57
Pathogenesis of congenital and autoimmune PAP?
Congenital: defect in type 2 pneumocytes Autoimmune: Defect in GM-CSF signaling pathway
58
Epithelium of esophagus?
Stratified squamous
59
Which layer absent in gallbladder & esophagus?
Esophagus: serosa/adventitia Gallbladder: submucosa
60
Infective esophagitis causes?
Candida CMV Herpes
61
Candida esophagitis gross & HPE?
Gross: Pseudomembranes Biopsy: pseudohyphae
62
Shallow ulcers in esophagus?
CMV
63
Punched out ulcers in esophagus?
Herpes
64
Biopsy of CMV ?
Owl eye inclusions (basophilic)
65
Biopsy findings of herpes esophagitis?
3Ms Multinucleation Moulding into one anaother Margination
66
Type of metaplasia seen in barrett esophagus?
Columnar epithelia metaplasia
67
Barrett esophagus increases risk of which cancer?
Adenocarcinoma
68
Special stain for barrett esophagus?
Alcian blue
69
Histological hallmark for barrett esophagus?
Intestinal metaplasia Goblet cells
70
Red velvety mucosa on endoscopy?
Barrett
71
Most common benign cancer of esophagus?
Leiomyoma
72
Most common cancer of esophagus 1.worldwide 2.western world?
1. Worldwide: squamous 2. Western world : adenocarcinoma
73
Squamous cancer affects which part of esphagus?
Upper 1/3 Middle 1/3 Lower 1/3 : adenocarcinoma
74
Risk factors of squamous esophagus cancer ?
HPV Smoking Alcohol Hot beverages SOX2 mutation Plummer vinson syndrome Preservation rich food Drugs/radiation Tylosis palmaris
75
Which factor is protective in adenocarcinoma of esophagus?
H.pylori
76
C/f of esophageal cancer?
Dysphagia (solids more than liquids) Anorexia Weight loss
77
Rat tail appearance on barium swallow?
Esophagus cancer
78
IHC markers of SCC?
Cytokeratin P63
79
Most important prognostic factor for esophageal cancer?
Depth of invasion
80
Esosinophilic keratin pearls seen in ?
Esophageal cancer hallmark
81
Portal triad?
Hepatic artery Portal vein Bile duct
82
What is space of disse?
Space between hepatocytes & sinusoidal ring
83
Sinusoids of liver lined by ?
Kupffer cells
84
hapatocytes have abundant eosinophilic cytoplasm due to what?
Increased mitochondria
85
1st site for amyloid deposition in liver?
Space of disse
86
Function of ito cells ?
Vitamin A storage Collagen synthesis
87
Stem cells of liver?
Oval cells
88
Most susceptible lobe of liver to ischemia ?
Zone 3 centrilobular
89
Jaundice causes UCB CB?
CB(direct): Dubin johnson, rotor, PBC, obstruction UCB: Crigler najjar, gilbert, hemolytic anaemia
90
Type of inheritance in crigler najjar 1 and 2 ?
CN-1 : AR CN-2 : AD
91
Crigler najjar 1 defect?
Complete deficiency of UGTA1
92
Defect in Gilbert?
Mild defect in UGTA1
93
Crigler najjar 2 defect?
Mild deficiency of UGTA1
94
Treatment of crigler najjar 2 ?
Phenobarbitone
95
Dark pigmented liver MRP2 defect Diagnosis?
Dubin johnson syndrome
96
Organic anion transport defect Non pigmented liver Diagnosis?
Rotor syndrome
97
Type of collagen in liver cirrhosis?
1 & 3
98
Liver cirrhosis causes ?
A : alcohol B : PBC,PSC C : cryptogenic cirrhosis D : drug induced cirrhosis E : enzyme induced(A1ATD) H : Hepatitis, hemochromatosis W : wilson disease