General oto esophageal dysphagia Flashcards

1
Q

In a patient with dysphagia, how can you differentiate oropharyngeal from esophageal dysphagia based on symptoms?

A

● Esophageal dysphagia: Food gets stuck after the swallow
is completed because of structural or neuromuscular
pathology; the problem is in the esophageal body or
lower esophageal sphincter.
● Oropharyngeal dysphagia: Difficult to complete swallow;
disorders involve the oropharynx, hypopharynx, and
upper esophageal sphincter.

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2
Q

How does the differential diagnosis change if a
patient with esophageal dysphagia complains of symptoms with solids only versus both solids and
liquids?

A

Mechanical obstruction usually causes difficulty with solids (but it may progress to involve liquids later on). Motility disorders commonly result in concurrent solid and liquid dysphagia.

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3
Q

What are the most common diagnoses in a patient

with solid-food esophageal dysphagia?

A

● Esophageal ring (intermittent)
● Peptic stricture (progressive)
● Malignancy (progressive)

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4
Q

What is the most common cause of acute

esophageal dysphagia?

A

Food impaction (meat); results in saliva expectoration

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5
Q

What disease process is characterized by decreased or absent lower esophageal sphincter relaxation and decreased or absent esophageal
peristalsis?

A

Achalasia (Greek: “does not relax”)

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6
Q

Eagle syndrome is associated with what anatomical abnormality?

A

Elongated styloid process (about > 3 cm) and/or ossification

or calcification of part or all the stylohyoid ligament. This syndrome was described in 1937 by Dr. Wyatt Eagle.

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7
Q

Dysphagia lusoria is associated with what anatomical anomaly?

A

Aberrant right subclavian artery

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8
Q

What histopathologic findings support the diagnosis of achalasia?

A

Decrease in total ganglion cells within the myenteric plexus,
the presence of T cell, eosinophil, and mast cell infiltration,
and increased neural fibrosis

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9
Q

What is the general age group most commonly

affected by achalasia?

A

20 to 60 years

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10
Q
What are the primary complaints associated with loss of lower esophageal sphincter relaxation and
esophageal aperistalsis (achalasia)?
A

Solid and liquid dysphagia, weight loss, chronic cough,

chest pain, hiccups, regurgitation, heartburn, and globus

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11
Q

What three associations are often included in
triple A syndrome (Allgrove syndrome), which is
most commonly found in children?

A

● Achalasia
● Adrenal insufficiency
● Alacrima

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12
Q

What infectious disease can lead to clinical

manifestations of achalasia?

A

Chagas disease

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13
Q

What management strategy can be used to reverse or stop the progression of achalasia?

A

None. The goal of management is to decrease lower

esophageal sphincter tone and manage reflux.

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14
Q

What is first-line therapy for patients with severe

achalasia?

A

Surgical dilation or myotomy unless the patient is a poor

operative candidate

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15
Q

What medical options are available for patients

with achalasia?

A

Nitrates and calcium channel blockers with the goal of

decreasing lower esophageal sphincter tone

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16
Q

What surgical interventions are available for

achalasia?

A

Good operative candidates may undergo pneumatic dilation or myotomy. Poor operative candidates may undergo dilation with a bougie or botulinum toxin injection.

17
Q

What pathogen is associated with Chagas disease?

A

Parasite Trypanosoma cruzi

18
Q

What is the vector for Trypanosoma cruzi?

A

Reduviid bugs

19
Q

Describe the esophageal manifestations of Chagas disease?

A

● Megaesophagus with dilation and muscular hypertrophy
● Reduction in the number of neurons in the myenteric
plexus

20
Q

What is the most common condition associated

with chronic Chagas disease?

A

● Cardiomyopathy
● Arrhythmias
● Conduction blocks

21
Q

What are the clinical manifestations of scleroderma?

A

Skin tightening, hyperpigmentation, and hypopigmentation
of skin, sclerodactyly, Raynaud phenomenon, GERD,
arthralgias, myalgias, Sicca syndrome, and dysphagia

22
Q

How common is esophageal involvement in

patients with scleroderma?

A

90%; 50% experience significant symptoms

23
Q

The progressive fibrosis and atrophy within the
smooth muscle of the esophagus associated with
scleroderma manifest with what classic finding on
esophageal manometry and barium esophagram?

A

● Manometry: Progressive loss of esophageal body peristalsis in distal two-thirds and decreased lower esophageal sphincter pressure
● Barium esophagram: Dilated esophagus, patulous gas-
troesophageal (GE) junction, and uninhibited reflux
events into the distal esophagus

24
Q

What are common complications noted in patients

with scleroderma and GERD?

A

Barrett esophagus, esophagitis, and strictures

25
Q

What laboratory test is most sensitive and specific

for dermatomyositis?

A

Creatine kinase

26
Q

How is dermatomyositis commonly treated?

A

Systemic steroid therapy and potentially immunosuppres-
sive and cytotoxic therapy, including methotrexate, aza-
thioprine, and cyclophosphamide

27
Q

Describe the potential head and neck manifestations of dermatomyositis.

A

Heliotrope discoloration of upper eyelids, malar rash,

dysphonia, dysphagia, scaly scalp, and hair loss

28
Q

What part of the aerodigestive tract is affected by

polymyositis?

A

Hypopharynx and upper third of the esophagus

29
Q

What is the cause of diffuse esophageal spasm?

A

Neural and muscular defects triggered by reflux events,
stress, extreme temperature variability in food or drink,
carbonation, or particular smells

30
Q

What symptoms are associated with diffuse

esophageal spasm?

A

Intermittent esophageal dysphagia, noncardiac chest pain,

reflux/heartburn

31
Q

What are the classic esophageal manometric
findings in patients with diffuse esophageal
spasms?

A

Two or more uncoordinated contractions during 10 consecutive swallows, aperistalsis in more than 30% of wet swallows, and a fifth of contractions being simultaneous