Cardiothoracic Disorders Flashcards

1
Q

What are the different types of coin lesions you can see on CXR?

A

Smooth walled (benign), calcium spicules (granuloma, malignant tumors are rarely calcified), bull’s eye (benign), spiculated surface (malignant, especially if > 3cm) and popcorn (benign hamartoma).

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2
Q

Chance of malignancy in a coin lesion in a patient age 50

A

50%. It increases with age.

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3
Q

Regions with coin lesions commonly due to coccidioidomycosis

A

SW USA

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4
Q

Regions with coin lesions commonly due to histoplasmosis

A

Mid Atlantic and Ohio Valley.

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5
Q

Tumors that commonly metastasize to the lungs and their 5-year survival

A

Testicular, breast (27-50%), renal (24-54%) and colon cancer (13-38%)

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6
Q

Next step in a patient with a SPN that is new from a prior CXR

A

CT to better characterize the lesion and look for lymphadenopathy. If suspicious CT-guided biopsy gets definitive dx 90% of the time.

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7
Q

Next step when CXR and CT reveal bronchial tree mass

A

Bronchoscopy for tissue sample and mediastinoscopy for assessment of lymph node involvement

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8
Q

What lung masses can simulate malignancy? How do you r/o malignancy with these masses?

A

ACTINOMYCOSIS: associated w/dental or sinus abscess and involves chest wall. COCCIDIOMYCOSIS: thin-walled cavity w/air-fluid level. HISTOPLASMOSIS: concentric or homogenous calcifications. BLASTOMYCOSIS: associated w/chronic skin ulcers. CRYPTOCOCCUS: superinfection in immunocompromised patient, meningeal involvement. ASPERGILLOSIS: mycetoma w/air crescent sign. HAMARTOMA: well defined border with slight lobulations (popcorn). ROUND ATELECTASIS: adjacent to thickened pleura w/comet tail vessel pattern.

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9
Q

Staging for non-small cell lung cancer and associated 5-year survival rates

A

Stage IA (50%): T1a/T1bN0M0 (< 3 cm across, only involves lung parenchyma and is > 2cm from main bronchus)

Stage IB (45%): T2aN0M0: 3-5cm, involves a main bronchus but > 2cm distal to carina, involves visceral pleura and/or partially obstructing airway.

Stage IIA (30%): T1a/T1bN1M0: < 3cm, does not involve visceral pleura or mainstem bronchi w/+ ipsilateral hilar LNs. OR T2aN1M0: 3-5cm, involves mainstem brochus but > 2cm distal to carina, involves visceral pleura and/or partially obstructing airway w/+ ipsilateral hilar LNs. OR T2bN0M0: 5-7cm, involves mainstem bronchus but > 2cm distal to carina, grown into visceral pleura and blocks the airways w/o LN spread.

Stage IIB (30%): T2bN1M0: 5-7cm, involves mainstem bronchus but > 2cm distal to carina, grown into visceral pleura and blocks the airways w/+ ipsilateral hilar LNs. OR T3, N0, M0: > 7cm, involves chest wall, diaphragm, mediastinal pleural, parietal pericardium, main bronchus < 2 cm from carina, airway obstruction leading to lung collapse or 2+ separate tumor nodules in same lobe. No +LNs.

Stage IIIA (15%): T1-T3N2M0: Any size, does not involve mediastinum, heart, great vessels, trachea, esophagus, spine, carina or different lobes. + ipsilateral hilar and/or mediastinal LNs. OR T3N1M0: > 7cm, involves chest wall, diaphragme, mediastinal pleura, parietal pericardium, main bronchus < 2cm to carina, 2+ nodules in same lobe, obstruction leading to lung collapse. +ipsilateral hilar LNs. OR T4N0/N1M0: Any size involving mediastinum, heart, great vessels, trachea, esophagus, spine carina and/or 2+ nodules in different lobes of same lung. +/- ipsilateral LNs.

Stage IIIB (5%): TanyN3M0: any size, obstruction leading to lung collapse, + supraclavicualr contralateral/ipsilateral mediastinal and hilar LNS. OR T4N2M0: any size involving mediastinum, heart, great vessels, trachea, esophagus, spine, carina, 2+ nodules in different lobes of same lung w/+ peribronchial LNs.

Stage IV (1%): TanyNanyM1a: metastasis to pleural and/or pericardial fluid. OR TanyNanyM1b: Metastasis to distant LNs, bone, brain, liver etc.

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10
Q

Lung cancer type with chemotherapy as the primary treatment

A

Small-cell carcinoma is a systemic disease at diagnosis because it has usually already spread beyond the lung and is not amenable to resection.

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11
Q

Lung cancer type with surgical resection as the primary treatment

A

Non-small cell carcinoma (adenocarcinoma and epidermoid carcinoma…aka squamous-cell carcinoma) are local diseases that spread to local and region LNs before becoming systemic.

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12
Q

What patients require a pneumonectomy over a lobectomy?

A

Centrally located tumors that involve mainstem bronchi. Note that pneumonectomy has a higher initial mortality rate and sleeve lobectomy, although more difficult, is an option if local invasion of the main pulmonary artery is not present.

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13
Q

Tx for stage I and II lung cancer

A

Surgical resection

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14
Q

Tx for stage III and IV lung cancer

A

Chemotherapy + radiation, then resection if chemoradiation sufficiently shrinks the tumor.

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15
Q

What is a pancoast tumor?

A

A tumor that grows in the superior sulcus of the lung. It invades the chest wall, lower cords of brachial plexus, subclavian artery and sympathetic ganglia. This can result in SOB, radiculopathies, peripheral limb ischemia and Horner’s syndrome.

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16
Q

Work up of a pancoast tumor

A

CT then bronchoscopy to check for bronchial invasion and get tissue if possible, mediastinoscopy to assess for LN spread and needle biopsy if tissue is still needed.

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17
Q

Tx for pancoast tumors

A

6 weeks radiation followed by surgical resection, patients do surprisingly well

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18
Q

Differential for small hemoptysis in a 25 year old non-smoker

A

Bronchial adenoma, atelectasis and Tb. These can all cause obstruction of a bronchus and bleeding.

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19
Q

Types of bronchial adenomas

A

These actually have considerable malignant potential: 1) Carcinoid, more benign when originating in lung, more malignant when originating from small bowel, may present with carcinoid syndrome. 2) Adenocystic carcinomas, which tend to invade locally.

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20
Q

Tx for bronchial adenomas

A

Lobectomy tends to be curative (except for when carcinoid metastasizes widely)

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21
Q

What do you worry about when you see a pleural effusion in an elderly patient?

A

Although effusions from CHF are more common, this is cancer (bronchogenic carcinoma or mesothelioma) until proven otherwise. After r/o cancer with thoracentesis and pleural biopsy you can consider other diagnoses like pneumonia, empyema or tuberculosis.

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22
Q

Mesothelioma on CT

A

Thick-walled tumor that is pleurally based

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23
Q

Tx for mesothelioma

A

En bloc pneumonectomy w/parietal and visceral pleura +/- pericardium and diaghragm. Morbidity and mortality rates are greater than 10%, but 30% of patient can recover. Chemorads is not an option.

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24
Q

How do you place a chest tube (tube thoracostomy)?

A

Make an incision between ribs 4 & 5 (at nipple line) above the rib. Finger dissect into the extrapleural space, then place a 24 Fr chest tube directed toward the apex and attach it to a water-seal-type drainage. If it is a patient’s 1st time pneumothorax you can consider a polyethylene tube with a one-way valve (Heimlich) over the 24 Fr tube and water seal.

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25
Q

Most common cause of the lung not expanding after placement of chest tube for pneumothorax?

A

Improperly placed chest tube. Try replacing the chest tube. If this does not fix the problem you then need to consider a parenchymal cause like leaking from large blebs/bronchi that need to be treated with pleurodesis to cause visceral and parietal pleura to adhere to each other.

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26
Q

Most common cause of empyema in the elderly

A

Strep pneumo in the community setting, Staph and gram-negs in the hospital setting. Anaerobes if pt has hx of aspiration pneumonia.

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27
Q

How do you treat a patient with empyema?

A

Abs, pus evacuation and lung re-expansion

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28
Q

Why is rapid tube thoracostomy important in the treatment of empyema

A

Over time the empyema can become loculated as fibrin organizes. If this occurs, the patient will require thoracotomy and decortication to re-expand the lung.

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29
Q

A patient presents with unstable angina. How do you treat him initially and how do you work him up?

A

Start with bed rest, sedation, 02, beta-blockers, nitroglycerin, aspirin and/or heparin. Check cardiac enzymes to r/o MI then do cardiac cath to check patency of coronary vessels.

30
Q

Normal EF

A

90% in kids, 70-80% in young adults and 50-60% in older people. < 40-50% is abnormal

31
Q

What is meant by three vessel disease? How do you treat a patient with three vessel disease and reduced EF?

A

Occlusion of the right coronary, LAD and the circumflex arteries (LAD and circumflex both branch off the left main). Treat with coronary bypass. This tx is indicated for left main disease (widowmaker) and 3-vessel disease w/reduced EF because it also has high mortality rates and these patients benefit more than any other group from bypass.

32
Q

How does PTCA compare to CABG?

A

In PTCA 30-60% of lesions reobstruct within 1 year so reoperation rates are higher early on.

33
Q

Best artery to use for CABG

A

Internal thoracic artery (internal mammary). 90%+ patency rates at 10 years.

34
Q

How does cardiopulmonary bypass work?

A

1) Clamp great vessels 2) Hyperosmolar (Na/Glc) w/K+ infused into heart for cardioplegia (blood and other buffers can be added to reduce ischemic acidosis and ROS damage). 3) Hypothermia to 86F (30C) in body, 59F (15C) in the heart. This combination allows the heart to be stopped for 2+ hours.

35
Q

Why would you ever consider off bypass coronary surgery with arterial anastomoses instead of the cardiopulmonary bypass machine?

A

The machine can generate a general infalmmatory response leading to respiratory, hemorrhagic and myocardial complications post-op. This is only considered in patients that are high-risk and patients with 1-2 easily accessible obstructed coronary arteries.

36
Q

Mortality rate for CABG

A

~3%

37
Q

What causes mitral valve regurgitation typically?

A

Myxomatous degeneration of the valve from ischemia to the mitral valve apparatus.

38
Q

Barlow syndrome

A

Mitral valve prolapse

39
Q

Common causes of mitral valve stenosis

A

Rheumatic and scarlet fever, this is why mitral valve stenosis is relatively rare in the US. Antibodies to group A strep also recognize the leaflets of the mitral valves. This causes fusion at the commissures and obstruction with late calcification. Increased left atrial pressure eventually leads to pulmonary HTN and right heart failure.

40
Q

How do we treat symptomatic mitral valve disease?

A

Commissurotomy can be done for stenosis if cought before calcifications of leafelets occurs. Annuloplasty (excising redundant leaflet and narrowing/reinforcing mitral annulus) is appropriate for prolapse. For either condition you can replace with a prosthetic valve.

41
Q

Causes of aortic stenosis

A

Congenital (from bicuspid valve), arteriosclerosis and deterioration.

42
Q

A patient presents with SOB, unstable angina and syncope. Echo shows aortic stenosis. What is this guy’s life expectancy if you don’t operate?

A

Dead within 2 years

43
Q

Work up in a patient with aortic stenosis

A

Cardiac cath to determine coronary circulation status, aortic valve lumen size, pressure gradient and ventricular function. You also need to do carotid doppler u/s to r/o carotid stenosis as the cause of syncope.

44
Q

Possible 1st symptom of aortic stenosis

A

Death in 5th or 6th decade.

45
Q

What determines the succes of aortic valve replacement in a patient with symptomatic high grade aortic stenosis?

A

Results of the catheterization…elderly patients typically do well regardless of age as long as they have preserved ventricular function.

46
Q

Options for aortic valve replacement

A

Mechanical (plastic/metal): durable, efficient and require anticoagulation for life. Tissue (human, porcine or bovine): do not require anticoagulation but require replacement around 7 years.

47
Q

Prognosis for patients suffering from dilated cardiomyopathy after a viral infection?

A

1/3 get better, 1/3 stay the same, 1/3 get worse

48
Q

Tx for dilated cardiomyopathy

A

Beta-blockers for symptomatic management. If condition continues to worsen, the patient will need a heart transplant.

49
Q

Prognosis for a patient receiving a hear transplant

A

Immediate survival = 90%. With immunosuppression (tacrolimus, cyclosporine and steroids) survival is 85-90% at 1 year and 75% at 2 years. Most deaths are due to infection from immunosuppression or rapid coronary atherosclerosis due to chronic rejection.

50
Q

Next step in a patient with recurrent regurgitation of undigested food

A

Barium swallow or upper endoscopy

51
Q

How do you get a Zenker diverticulum?

A

It is a pulsion diverticulum, meaning that pressure from swallowing causes mucosa to pouch out between the inferior pharyngeal constrictor superiorly and the cricopharyngeal inferiorly.

52
Q

Where in the esophagus can you get a pulsion diverticulum aside from Zenker?

A

Distal esophagus near the GE junction, called an epiphrenic diverticulum. At attachments outside of esophagus, called a traction diverticulum.

53
Q

Tx for esophageal diverticuli

A

Transection of the cricopharyngeal muscle to relax the esophageal entrance. Excision and esophageal myotomy are necessary with epiphrenic diverticuli.

54
Q

Why is a bird’s beak esophagus so characteristic of dysphagia?

A

Whatever the etiology (T. cruzi, stress, trauma or weight loss), there is loss of the Auerbach plexus (parasympathetic ganglion in esophageal smooth muscle) which prevents esophageal peristalsis and LES relaxation. Food then gets stuck and the esophagus becomes an adynamic sac.

55
Q

What is the treatment for achalasia?

A

Ca-channel blockers can induce LES relaxation; however, correction is typically surgical w/ Heller myotomy (100% relief) or endoscopically w/ balloon dilation (60% relief)

56
Q

Esophageal tumors typically found in the upper and middle 1/3 of the esophagus

A

Squamous cell carcinoma

57
Q

Esophageal cancers typically found in the lower 1/3 of the esophagus

A

Can often be squamous cell, but incidence of adenocarcinoma is increasing b/c of GERD -> squamous cell dysplasia to columnar cells -> Barrett’s esophagus (shown below) -> Adenocarcinoma.

58
Q

How is squamous cell esophageal carcinonma staged?

A

T, N, M, G.

Stage 0: Tis, N0, M0, GX or G1; any location: This is the earliest stage of esophageal cancer. It is also called high-grade dysplasia. The cancer cells are found only in the epithelium (the layer of cells lining the esophagus). The cancer has not grown into the connective tissue beneath these cells (Tis). The cancer has not spread to nearby lymph nodes (N0) or other organs (M0). The tumor is well differentiated (G1) or grade information is not available (GX), and it can be anywhere along the esophagus.

Stage IA: T1, N0, M0, GX or G1; any location: The cancer has grown from the epithelium into the layers below, such as the lamina propria, muscularis mucosa, or submucosa, but it has not grown any deeper (T1). It has not spread to nearby lymph nodes (N0) or to distant sites (M0). The tumor is well differentiated (G1) or grade information is not available (GX). It can be anywhere along the esophagus.

Stage IB: Either of the following:

T1, N0, M0, G2 or G3; any location: The cancer has grown from the epithelium into the layers below, such as the lamina propria, muscularis mucosa, or submucosa, but it has not grown any deeper (T1). It has not spread to nearby lymph nodes (N0) or to distant sites (M0). It is moderately (G2) or poorly differentiated (G3). The tumor can be anywhere in the esophagus.

T2 or T3, N0, M0, GX or G1; location lower: The cancer has grown into the muscle layer called the muscularis propria (T2). It may also have grown through the muscle layer into the adventitia, the connective tissue covering the outside of the esophagus (T3). The cancer has not spread to nearby lymph nodes (N0) or to distant sites (M0). It is well differentiated (G1) or grade information is not available (GX). Its highest point is in the lower part of the esophagus.

Stage IIA: Either of the following:

T2 or T3, N0, M0, GX or G1; location upper or middle: The cancer has grown into the muscle layer called the muscularis propria (T2). It may also have grown through the muscle layer into the adventitia, the connective tissue covering the outside of the esophagus (T3). The cancer has not spread to nearby lymph nodes (N0) or to distant sites (M0).The cancer is in the upper or middle part of the esophagus and is well differentiated (G1) or grade information is not available (GX).

T2 or T3, N0, M0, G2 or G3; location lower: The cancer has grown into the muscle layer called the muscularis propria (T2). It may also have grown through the muscle layer into the adventitia, the connective tissue covering the outside of the esophagus (T3). The cancer has not spread to lymph nodes (N0) or to distant sites (M0).The cancer is in the lower part of the esophagus and is moderately (G2) or poorly differentiated (G3).

Stage IIB: Either of the following:

T2 or T3, N0, M0, G2 or G3; location upper or middle: The cancer has grown into the muscle layer called the muscularis propria (T2). It may also have grown through the muscle layer into the adventitia, the connective tissue covering the outside of the esophagus (T3). The cancer has not spread to nearby lymph nodes (N0) or to distant sites (M0). It is in the upper or middle part of the esophagus and is moderately (G2) or poorly differentiated (G3).

T1 or T2, N1, M0, any G; any location: The cancer has grown into the layers below the epithelium, such as the lamina propria, muscularis mucosa, or submucosa (T1). It may also have grown into the muscularis propria (T2). It has not grown through to the outer layer of tissue covering the esophagus. It has spread to 1 or 2 lymph nodes near the esophagus (N1) but has not spread to lymph nodes further away from the esophagus or to distant sites (M0). It can be any grade (G) and can be anywhere along the esophagus.

Stage IIIA: Any of the following:

T1 or T2, N2, M0, any G; any location: The cancer has grown into the layers below the epithelium, such as the lamina propria, muscularis mucosa, or submucosa (T1). It may also have grown into the muscularis propria (T2). It has not grown through to the outer layer of tissue covering the esophagus. It has spread to 3 to 6 lymph nodes near the esophagus (N2) but it has not spread to lymph nodes farther away from the esophagus or to distant sites (M0). It can be any grade (G) and can be anywhere along the esophagus.

T3, N1, M0, any G; any location: The cancer has grown through the wall of the esophagus to its outer layer, the adventitia (T3). It has spread to 1 or 2 lymph nodes near the esophagus (N1), but it has not spread to lymph nodes farther away from the esophagus or to distant sites (M0). It can be any grade (G) and can be anywhere along the esophagus.

T4a, N0, M0, any G; any location: The cancer has grown all the way through the esophagus and into nearby organs or tissues (T4a) but still can be removed. It has not spread to nearby lymph nodes (N0) or to distant sites (M0). It can be any grade (G) and can be anywhere along the esophagus.

Stage IIIB: T3, N2, M0, any G; any location: The cancer has grown through the wall of the esophagus to its outer layer, the adventitia (T3). It has spread to 3 to 6 lymph nodes near the esophagus (N2), but has not spread to lymph nodes farther away from the esophagus or to distant sites (M0). It can be any grade (G) and can be anywhere along the esophagus.

Stage IIIC: Any of the following:

T4a, N1 or N2, M0, any G; any location: The cancer has grown all the way through the esophagus and into nearby organs or tissues (T4a) but still can be removed. It has spread to 1 to 6 lymph nodes near the esophagus (N1 or N2), but it has not spread to lymph nodes farther away from the esophagus or to distant sites (M0). It can be any grade (G) and can be anywhere along the esophagus.

T4b, any N, M0, any G; any location: The cancer cannot be removed with surgery because it has grown into the trachea (windpipe), the aorta (the large blood vessel coming from the heart), the spine, or other crucial structures (T4b). It may or may not have spread to nearby lymph nodes (any N), but it has not spread to lymph nodes farther away from the esophagus or to distant sites (M0). It can be any grade (G) and can be anywhere along the esophagus.

Any T, N3, M0, any G; any location: The cancer has spread to 7 or more nearby lymph nodes (N3), but it has not spread to lymph nodes farther away from the esophagus or to distant sites (M0). It can be any grade and can be anywhere along the esophagus.

Stage IV: Any T, any N, M1, any G; any location: The cancer has spread to distant lymph nodes or other sites (M1). It can be any grade (G) and can be anywhere along the esophagus.

59
Q

How is adenocarcinoma of the esophagus staged?

A

Stage 0: Tis, N0, M0, GX or G1: This is the earliest stage of esophageal cancer. It is also called high-grade dysplasia. The cancer cells are found only in the epithelium (the layer of cells lining of the esophagus). The cancer has not grown into the connective tissue beneath these cells (Tis). The cancer has not spread to nearby lymph nodes (N0) or other organs (M0). It is well differentiated (G1) or grade information is not available (GX).

Stage IA: T1, N0, M0, GX, G1, or G2: The cancer has grown from the epithelium into the layers below, such as the lamina propria, muscularis mucosa, or submucosa, but it has not grown any deeper (T1). It has not spread to nearby lymph nodes (N0) or to distant sites (M0). It is well (G1) or moderately differentiated (G2), or grade information is not available (GX).

Stage IB: Either of the following:

T1, N0, M0, G3: The cancer has grown from the epithelium into the layers below, such as the lamina propria, muscularis mucosa, or submucosa, but it has not grown any deeper (T1). It has not spread to nearby lymph nodes (N0) or to distant sites (M0). It is poorly differentiated (G3).

T2, N0, M0, GX, G1, or G2: The cancer has grown into the muscle layer called the muscularis propria (T2). It has not spread to nearby lymph nodes (N0) or to distant sites (M0). It is well (G1) or moderately differentiated (G2), or grade information is not available (GX).

Stage IIA: T2, N0, M0, G3: The cancer has grown into the muscle layer called the muscularis propria (T2). It has not spread to nearby lymph nodes (N0) or to distant sites (M0). It is poorly differentiated (G3).

Stage IIB: Either of the following:

T3, N0, M0, any G: The cancer has grown through the wall of the esophagus to its outer layer, the adventitia (T3). It has not spread to nearby lymph nodes (N0) or to distant sites (M0). It can be any grade.

T1 or T2, N1, M0, any G: The cancer has grown into the layers below the epithelium, such as the lamina propria, muscularis mucosa, or submucosa (T1). It may also have grown into the muscularis propria (T2). It has not grown through to the outer layer of tissue covering the esophagus. It has spread to 1 or 2 lymph nodes near the esophagus (N1), but it has not spread to lymph nodes farther away from the esophagus or to distant sites (M0). It can be any grade.

Stage IIIA: Any of the following:

T1 or T2, N2, M0, any G: The cancer has grown into the layers below the epithelium, such as the lamina propria, muscularis mucosa, or submucosa (T1). It may also have grown into the muscularis propria (T2). It has not grown through to the outer layer of tissue covering the esophagus. It has spread to 3 to 6 lymph nodes near the esophagus (N2) but it has not spread to lymph nodes farther away from the esophagus or to distant sites (M0). It can be any grade (G).

T3, N1, M0, any G: The cancer has grown through the wall of the esophagus to its outer layer, the adventitia (T3). It has spread to 1 or 2 lymph nodes near the esophagus (N1), but it has not spread to lymph nodes farther away from the esophagus or to distant sites (M0). It can be any grade (G).

T4a, N0, M0, any G: The cancer has grown all the way through the esophagus and into nearby organs or tissues (T4a) but still can be removed. It has not spread to nearby lymph nodes (N0) or to distant sites (M0). It can be any grade (G).

Stage IIIB: T3, N2, M0, any G: The cancer has grown through the wall of the esophagus to its outer layer, the adventitia (T3). It has spread to 3 to 6 lymph nodes near the esophagus (N2), but it has not spread to lymph nodes farther away from the esophagus or to distant sites (M0). It can be any grade (G).

Stage IIIC: Any of the following:

T4a, N1 or N2, M0, any G: The cancer has grown all the way through the esophagus and into nearby organs or tissues (T4a) but still can be removed. It has spread to 1 to 6 lymph nodes near the esophagus (N1 or N2), but it has not spread to lymph nodes farther away from the esophagus or to distant sites (M0). It can be any grade (G).

T4b, any N, M0, any G: The cancer cannot be removed with surgery because it has grown into the trachea (windpipe), the aorta (the large blood vessel coming from the heart), the spine, or other crucial structures (T4b). It may or may not have spread to nearby lymph nodes (any N), but it has not spread to lymph nodes farther away from the esophagus or to distant sites (M0). It can be any grade (G).

Any T, N3, M0, any G: The cancer has spread to 7 or more nearby lymph nodes (N3), but it has not spread to lymph nodes farther away from the esophagus or to distant sites (M0). It can be any grade (G).

Stage IV: Any T, any N, M1, any G: The cancer has spread to distant lymph nodes or other sites (M1). It can be any grade (G).

60
Q

What esophageal cancers are resectable.

A

Stages I and II. Most stage IIIs are resectable as long as the cancer has not grown into the trachea, the aorta, spine, or other nearby crucial structures. Many stage IIIs that are potentially resectable are not because patients are not healthy enough.

61
Q

What are the 5 year survival rates for esophageal cancer?

A

Localized to esophagus = 40%. Regional spread = 21%. Distant spread = 4%.

62
Q

By what physical means is esophageal cancer staged?

A

Endoscopic u/s to assess tumor depth and local LN involvement. Chest and abdomen CT to assess for celiac node spread and abdominal involvement. Note the layers of the esophagus on the endoscopic u/s below: 1st hyperechoic layer: interface between lumen and mucosa, 2nd hypoechoic layer: deep mucosa and muscularis mucosa, 3rd hyperechoic layer: submucosa, 4th hypoechoic layer: muscularis propria, 5th hyperechoic layer: adventitia/fat interface

63
Q

Treatment for esophageal cancer

A

If upper 1/3 of esophagus = chemoradiation followed by resection of obstruction persists. If middle 1/3 of esophagus = neoadjuvant chemoradiation followed by surgical resection if tumor shrinks appropriately (because these tumors often invade local structures). If lower 1/3 of esophagus = esophagectomy and proximal gastrectomy with intrathoracic esophagogastric anastamosis.

64
Q

What are the 2 types of esophagectomy that can be performed for esophageal cancer? Why choose one over the other?

A

Formal esophagectomy (Ivor Lewis): upper abdominal incision + right thoracotomy -> gastroesophageal anastamosis in chest, can also convert to neck, advantage of keeping most gastric mucosa. Transhiatal esophagectomy: incision in neck + incision in upper abdoment -> upper esophagectomy + sleeve gastrectomy -> anastomosis of stomach and esophagus in neck, this procedure is good because risk of anastomosis leak is 10% and if it leaks in the chest there is a higher risk for infection and pulmonary complications.

65
Q

How do you confirm your diagnosis in a patient presenting with signs and symptoms of dysphagia that are concerning for esophageal cancer?

A

Barium swallow, esophagoscopy and biopsy

66
Q

Why might a patient with squamous cell esophageal carcinoma have a cough as an associated symptom?

A

Erosion of esophageal mucosa can create a TEF and cause aspiration

67
Q

Since 80% of patients will die in their first year after diagnosis of esophageal cancer, what measures can you do that are not curative, but palliative?

A

Feeding gastrostomy (G-tube), esophageal stents, radiation or palliative resection. Just know that mortality rate and complications increase with each of these procedures.

68
Q

What tumors commonly originate in the anterior mediastinum and how do they present?

A

Thymus tumor 33% (+/- myasthenia gravis), lymphoma 19% (most common is Hodgkin lymphoma in young people), germ cell 17% (teratomas most common = calcium deposits, hair, primitive teeth), carcinoma 11%, cysts 8%, mesenchymal 4%, and endocrine 6%.

69
Q

When is surgery appropriate for a tumor in the anterior mediastinum?

A

Thymomas and other non-lymphoma tumors. Lymphomas are treated with chemoradiation.

70
Q

What are the common tumors of the middle mediastinum? How do you manage them?

A

Cysts account for 61% of them. Bronchiogenic cysts (from foregut remnants, lined w/columnar epithelium) and pericardial cysts (water bottle appearance). Because cysts can become inflammed, symptomatic and form fistulas, surgical excision is appropriate. Lymphomas 21%, mesenchymal 8% and carcinoma 6% of tumors.

71
Q

What are the common tumors of the posterior mediastinum? How do you treat them?

A

Neurogenic tumors (53%) adjacent to vertebral bodies (neurilemoma is most common and most are benign (41%)). Cysts (32%), mesenchymal tumors (9%) and endocrine tumors (2%) also occur. Tumors can be dumbell-shaped, inside the spinal canal or outside the spinal canal. After confirming tumor w/imaging, removal by thoracic and neurosurgical approach are warranted.