Lec 8 Lung tumors I Flashcards

1
Q

Peak incidence of lung tumors:

A

50s-60’s

presented in late stages

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2
Q

Diagnostic techniques for lung cancer:

A

-Chest X ray
-sputum cytology
-bronchial biopsy
-trans bronchial biopsy
-transcutaneous needle biopsy
-open lung biopsy (invasive)

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3
Q

Primary Lung tumors:

A

95% NSCLC

M:F 2:1

5% are bronchial carcinoids and bronchial gland tumors:
-rare mesenchymal tumors and lymphomas
-Hamartoma: Most common benign primary tumor

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4
Q

Etiology of lung cancer:

A

1)smoking- squamous and small cell carcinoma 90%
2)Occupational hazards
3)scarring in lung tissue

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5
Q

Genetic mutation of lung cancers:

A

**4)Genetic mutations **
-Inactivation of supressor gene on chr.3p and later mutations in TP53
-Activating mutations EGFR,KRAS,ALK,ROS1, HER2 or c-MET in adenocarcinoma
-RB mutation in small cell carcinoma
-p16/CDKN2A inactivation in NSCLC’s

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6
Q

Clinical manifestations:

A

**Central or endobronchial tumor growth: **(small cell carcinoma)
-cough, hemoptysis,wheeze,stridor, dyspnea and post productuve pneumonitis.

periphral tumor growth: (adenocarcinomas)
Chest pain,cough, dyspnea, pneumonia like symptoms

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7
Q

Gross appearance:

A

Central masses: carcinoma in situ with endobronchial growth: squamous and small cell CA

-Periphral nodules: consolidative pleural involvment:
adenocarcinomas and large cell carcinomas

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8
Q

NSCLC:

1)squamous cell carcinoma:

male: female affects who the most, location

A

-Male>female
-smoker associated
-Central, may show cavitation —– bronchoscope
-P40 and CK5/6

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9
Q

2)Adenocarcinoma:

most common in who, location, growth speed, mutations are:

A

-most common in females
-Least associated with smoking
-periphral
-slow growing but widely metastatic

-3p deletion and KRAS mutation in AAH
-TTF-1 positive by IHC

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10
Q

Histology of squamous cell CA:

formation of what, spreads to what?, associated with?

A

-squamous differentiation and keratin formation
-spreads to local and regional lymph nodes

-metasases later than small cell
-may be associated with hypercalcemia

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11
Q

2 histologic types of Adenocarcinoma:

A

1)Invasive:
-Acinar
-Papillary
-mucinous
-solid

2)Adenocarcinoma in situ
-localized nodule or multifocal
-growth along alveolar walls

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12
Q

3) large cell carcinoma:

A

-poorly differentiated tumors
-aka poorly differentiated squamous cell CA or adenocarcinoma
-poor prognosis

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13
Q

Small cell carcinoma: SCLC

general features

A

male>female
smoker dominant
arises from neuroendocrine cells

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14
Q

SCLC cytology:

A

-Crush artifact
-nuclear molding

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15
Q

SCLC features:

A

location- central
spreads widely in lung
aggressive with necrosis
metastizes early
most frequent type with ectopic hormones

responsive to chemotherapy

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16
Q

SCLC histology:

A

small blue cells
azzopardi effect
positive for TTF-1

17
Q

spread of lung cancer can be:

A

1)local (minority) (like in squamous cell CA)
pleura, pericaridum, mediastinum, nerves vessles

2)lymphnode metastasis (also in squamous cell CA)
-regional lymph node , bronchial, trachial, mediastinal

3)distant (most of cancers)
adrenal (>50%), liver, brain,bone

18
Q

Local effects of cancer:

A

Central- cough, wheezing, hemoptysis
periphral- incidental hemoptysis or pneumonia

19
Q

regional invasion;

A

Recurrent pharyngeal nerve: vocal cord paralysis

Phrenic nerve: diaphragmatic paralysis

esophagus: bronchoesophageal fistula

Chest wall invasion: pain and pleural effusion

20
Q

Invasion of upper lobe:

A

right upper lobe invasion– superior vena cava syndrome

Apical tumor– pain and destruction of first and second rib+ vertebra

cervical sympathetic plexus— horner syndrome

21
Q

paraneoplastic syndrome: hyper calcemia

A

:hypercalcemia:
caused by PTHrP production- squamous cell CA
-kidney stones
-constipation and fatigue if moderate
-coma and arrythmias is severe

22
Q

Paraneoplastic syndrome: Cushing syndrome

A

due to ectopic ACTH production

patient presents with:
-fluid retention
-increased facial hair
-moon like face

SCLC related

23
Q

paraneoplastic syndromes: Digital clubbing

A

-can result from hypertrophic osteoarthropathy

24
Q

```

paraneoplastic syndromes: neuromuscular disorders

A

myasthenic syndromes
neuropathy and polymyositis
seen in SCLC

25
Q

Paraneoplastic syndromes: migratory thrombophlebitis

A

Common cause of DIC in adenocarcinoma

26
Q

Lung hamartoma- benign lung lesion

A

Most common

-Coin lesoin on X ray
-abscess but benign

27
Q

Metastatic lung tumors show:

A

-Multiple discrete nodules (cannon ball)
-single nodules
-lymphaginitis carcinomatosa
-pleural effusion

28
Q

Malignant mesotholemia gross:

A

-starts as pleural fibrosis and palque

-later as gelatinous yellowish white tumor ensheathing the lung.

poor prognisis

29
Q

Malignant mesotholemia casued by:

A

inactivation of multiple supperssor genes: p53,RB,BAP1