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DYSPHAGIA

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Title: DYSPHAGIA


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DYSPHAGIA
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Question 1
  • A 51 yr.old female presented with a hx of
    dysphagia that has been progressively worsening
    for months. Initially dysphagia was for solids
    only but more recently it is for both solids and
    liquids.
  • Which of the following studies will most likely
    establish the diagnosis
  • EGD
  • Barium swallow
  • CT
  • manometry

3
Question-2
  • A 52 year-old male executive c/o intermittent
    dysphagia which began 2 years ago. When he is
    eating, he has episodes of the sudden sensation
    of food sticking in his throat after he swallows,
    lower chest discomfortand hypersalivation. On two
    occassions the discomfort has caused him to
    regurgitate undigested food. There is now wt
    loss.Physical exam is normal
  • The most likely diagnosis is
  • Achalasia
  • Diffuse esophageal spasm
  • Esophageal ring
  • Peptic stricture
  • Adenocarcinoma

4
INTRODUCTION
  • Dysphagiadifficulty with swallowingis a common
    condition, reported by 58 of the general
    population aged over 50 years, and by 16 of the
    elderly.
  • Dysphagia, particularly oropharyngeal dysphagia,
    is even more common in the chronic-care setting
    up to 60 of nursing-home occupants have feeding
    difficulties that include dysphagia.

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ESOPHAGEAL ANATOMY
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ESOPHAGEAL ANATOMY
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SWALLOWING
  • Mechanism is complex
  • Involves the actions of 26 muscles and 5 cranial
    nerves
  • CN V -- both sensory and motor fibers important
    in chewing
  • CN VII -- both sensory and motor fibers
    important for sensation of oropharynx taste to
    anterior 2/3 of tongue
  • CN IX -- both sensory and motor fibers important
    for taste to posterior tongue, sensory and motor
    functions of the pharynx
  • CN X -- both sensory and motor fibers important
    for taste to oropharynx, and sensation and motor
    function to larynx and laryngopharynx important
    for airway protection
  • CN XII -- motor fibers that primarily innervate
    the tongue
  • A normal adult swallows unconsciously 600 times
    in a 24-hour period

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Esophageal Anatomy
  • Upper one-third is composed of skeletal muscle
  • Distal two-thirds is smooth muscle
  • NO SEROSA
  • Outer longitudinal, inner circular muscle layer
  • Myenteric plexus of Auerbach, parasympathetic
    ganglion cells, interspersed among the muscle
    layers
  • Submucosa blood vessels/lymphatics, myenteric
    plexus of Meissner (parasympathetic ganglion
    cells)
  • Mucosa stratified squamous epithelium

11
REVIEW
  • The outermost collection, lying between the inner
    circular and outer longitudinal smooth-muscle
    layers of the gut, is called the myenteric (or
    Auerbach's) plexus.
  • Neurons of this plexus regulate the peristaltic
    waves, consisting of polarized muscular activity,
    that move digestive products from oral to anal
    openings.
  • In addition, myenteric neurons control local
    muscular contractions that are responsible for
    stationary mixing and churning.
  • The innermost group of neurons is called the
    submucosal (or Meissner's) plexus. This group
    regulates the configuration of the luminal
    surface, controls glandular secretions, alters
    electrolyte and water transport, and regulates
    local blood flow

12
Swallowing Stage 1
  • Oral
  • Food ingested, prepared (mastication) and
    modified (lubrication)
  • Voluntary control
  • Frequently results from weakness lips, tongue,
    cheeks
  • Unable to organize food into well formed bolus
    and move posteriorly
  • Xerostomia difficulty breaking down solids

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Swallowing Stage 2
  • Pharyngeal
  • Prevented from entering nasopharynx, larynx
    rises, retroflexion of epiglottis and vocal fold
    closure, synchronized contraction of middle and
    inferior constrictors, and synchronized
    relaxation of the cricopharyngeal muscle
    Involuntary
  • Timing neurologic epiglottis doesnt protect
    larynx - leads to cough/aspiration
  • Weakness neurologic injury/cancer residual
    food after swallow can lead to aspiration

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Stage 3
  • Esophageal
  • Begins with crico-pharyngeal relaxation
  • Involuntary
  • Most common
  • Sensation of food sticking at base of
    throat/chest
  • Peristalsis, tumor, stricture

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HISTORY
  • Taking a careful history is vital for the
    evaluation of dysphagia.
  • The history will yield the likely underlying
    -pathophysiologic process
    -anatomic site of the problem in most
    patients-80
    -crucial for determining whether
    subsequently detected radiographic or
    endoscopic 'anomalies' are relevant or
    incidental..

17
HISTORY
  • Three fundamental aims should be met when taking
    a dysphagia history.
  • -The first is to establish whether or not
    dysphagia is actually present that is, to
    distinguish true dysphagia from globus
    sensation (in b/w meals), xerostomia-loose
    the lubrication properties and stimulus odynophag
    ia-transient than dysphagia, and persists only
    during the 1530 s that a bolus takes to
    traverse the esophagus.
  • -The second is to determine whether the site of
    the problem is esophageal or pharyngeal
  • -The third is to distinguish a structural
    abnormality from a motor disorder These avenues
    of enquiry are outlined below in an order that
    corresponds to that of a highly effective
    diagnostic algorithm.
  • The history will also dictate whether the next
    diagnostic procedure should be endoscopy, a
    barium swallow or esophageal manometry. In some
    difficult cases, all three diagnostic techniques
    may need to be performed to establish an accurate
    diagnosis.

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Where is the site of bolus hold-up?
  • Retrosternal bolus hold-up indicates that the
    disorder lies within the esophagus.
  • However, the patient's perception of an apparent
    bolus hold-up in the neck has low diagnostic
    specificity, and cervical localization per se
    does not help the clinician to distinguish
    pharyngeal from esophageal causes of dysphagia.
  • Owing to viscerosomatic referral, in 30 of cases
    the perceived site of hold-up is above the
    suprasternal notch when the actual hold-up is
    within the esophageal

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Does the patient report symptoms that are
predictive of oropharyngeal dysfunction
  • there are four symptoms that have high
    specificity for oropharyngeal dysfunction
    -delayed or absent oropharyngeal swallow
    initiation -deglutitive postnasal
    regurgitation or egress of fluid
    through the nose during swallowing
    -deglutitive cough indicative of aspiration and
    -the need to swallow repetitively to achieve
    satisfactory clearance of swallowed
    material from the hypopharynx.
  • If one or more of these four symptoms are present
    then the cause of dysphagia is probably
    oropharyngeal, either structural or neuromyogenic

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OROPHARYNGEAL VS ESOPHAGEAL
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Etiology of oropharyngeal dysphagia. 
  • Structural
  •   Tumor
  •   Stenosis
  • Postsurgical
  • Radiation
  • Idiopathic
  •   Zenker's diverticulum
  •   Cricopharyngeal bar
  •   Web
  •   Extrinsic compression
  •  
  • Neuromyogenic
  •   Stroke
  •   Head trauma
  •   Parkinson's disease and parkinsonism
  •   Amyotrophic lateral sclerosis
  •   Multiple sclerosis
  •   Myasthenia gravis
  •   Myopathies (inflammatory, metabolic)

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ESOPHAGEAL
  • Structural disorders
  • Inflammatory and/or fibrotic strictures
  • Peptic
  • Caustic
  • Pill-induced
  • Radiation-induced
  • Mucosal rings and webs
  • Schatzki's ring
  • Multiringed esophagus (eosinophilic
    esophagitis)
  • Carcinoma
  • Primary (squamous, adenocarcinoma)
  • Secondary (e.g. breast, melanoma)

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  • Disorders related to systemic diseases
  • Pemphigus and pemphigoid conditions
  • Lichen planus
  • Scleroderma (multifactorial)
  • Intramural lesions
  • Leiomyoma
  • Granular cell tumor
  • Extramural lesions
  • Aberrant right subclavian artery (dysphagia
    lusoria)
  • Mediastinal masses
  • Bronchial carcinoma
  • Anatomical abnormalities
  • Hiatal hernia
  • Esophageal diverticulum

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  • Motility disorders
  • Achalasia and achalasia-like disorders
  • Idiopathic (classic) achalasia
  • Atypical disorders of lower esophageal
    sphincter relaxation
  • Chagas disease
  • Pseudoachalasia

25
ESOPHAGEAL
  • Differntiation mechanical vs motility
    disorder?

26
Is the dysphagia for solids or liquids
  • Patients who have a motor disorder will describe
    dysphagia for liquids and solids,
  • Whereas patients who have structural disorders
    will describe dysphagia for solids only.
  • Once a solid bolus becomes impacted, the patient
    will report dysphagia for liquids and solids,

27
Motility- features
  • Three cardinal features of dysmotility
    dysphagia (for solids and liquids), chest
    pain and
    regurgitation.
  • Regurgitation during meals, as well as
    spontaneous regurgitation between meals or at
    night, is highly suggestive of dysmotility.
  • Unlike regurgitation that is related to GERD,
    the regurgitated fluid in patients with
    esophageal dysmotility is generally not noxious
    to taste.
  • In addition, spasm or achalasia typically cause
    chest pain. Although this chest pain is
    frequently described as 'heavy' or 'crushing', it
    can be indistinguishable from the typical
    'heartburn' of reflux.
  • The pain frequently occurs during meals, but it
    can be quite unpredictable and sporadic or
    nocturnal.
  • Sipping antacids or even water can relieve the
    pain related to dysmotility, which further
    confuses its distinction from reflux-related pain.

28
How long has dysphagia been present? Is it
intermittent? Is it progressive?
  • Slowly progressive, long-standing dysphagia,
    particularly against a background of reflux, is
    suggestive of a peptic stricture.
    Caveat -severity of heartburn correlates
    poorly with esophageal mucosal damage. For
    example, patients who have severe mucosal
    changes, including strictures and Barrett's
    mucosa, could have had minimal or no heartburn in
    the immediate past.
  • A short history of dysphagiaparticularly with
    rapid progression (weeks or months) and
    associated weight lossis highly suggestive of
    esophageal cancer.
  • Long-standing, intermittent, nonprogressive
    dysphagia purely for solids is indicative of a
    fixed structural lesion such as a distal
    esophageal ring or proximal esophageal mucosal
    web.

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Examination of the patient with dysphagia
  • The physical examination is generally
    unremarkable.
  • Skin should be examined for features of
    connective tissue disorders, particularly
    scleroderma and CREST (calcinosis, Raynaud's
    phenomenon, esophageal dysmotility, sclerodactyly
    and telangiectasia) syndrome.
  • Muscle weakness or wasting might be evident if
    myositis is present, and myositis can overlap
    with other connective tissue disorders that
    affect the esophagus.
  • Signs of malnutrition, weight loss and pulmonary
    complications from aspiration should be looked
    for.
  • If pharyngeal dysphagia is suspected, evaluation
    for neuromuscular disorders is important

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Investigation of esophageal dysphagia
  • Barium swallow study,
  • Endoscopy and
  • Esophageal manometry.

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NO DYSPHAGIA
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INTERMITTENT DYSPHAGIA FOR SOLIDS
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DYSPHAGIA WITH LONG HX OF GERD
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Bulge in the left side of the neck while eating
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DYSPHAGIA FOR SOLIDS AND LIQUIDS WITH WT LOSS
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DYSPHAGIA FOR SOLIDS AND LIQUIDS
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young male patients who present with intermittent
dysphagia or bolus impaction
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INTERMITTENT DYSPHAGIA FOR SOLIDS AND LIQUIDS
  • Numerous nonpropulsive contractions
  • corkscrew/ rosary bead esophagus

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INTERMITTENT DYSPHAGIA FOR SOLIDS
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IRON DEFIIENCY ANEMIA
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Due to an aberrant right subclavian artery
coursing posterior to esophagus
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