Esophagus-path/icm Flashcards

1
Q

What is Atresia?

A

Incomplete development

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2
Q

What is the most common congenital anomalies of esophagus?

A

Esophageal Atresia/Tracheoesophageal Fistula

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3
Q

What are are the clinical sx of Atresia/Tracheoesophageal Fistula?

A

aspiration
suffocation
pneumonia
fluid and electrolyte imbalances

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4
Q

When are Atresia/Tracheoesophageal Fistula diagnosed?

A

regurgitation during feeding

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5
Q

what can Atresia/Tracheoesophageal Fistula be associated with?

A

with heart and GU malformations

also..congential stenosis of esophagus and S.I.

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6
Q

What are the 3 types of Esophageal dysmotility?

A
  • Nutcracker esophagus
  • Diffuse esophageal spasm
  • Hypertensive lower esophageal sphincter
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7
Q

What is Nutcracker esophagus?

A

high amplitude contractions of distal esophagus (loss of coordination btw inner circular layer and outer longitudinal layer)

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8
Q

What is Diffuse esophageal spams?

A

repetitive simultaneous contractions of distal esophageal esophagus

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9
Q

What is hypertensive lower esophageal sphincter?

A

no contraction problems

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10
Q

How do you diagnose esophageal dysmotility?

A

esophageal manometry

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11
Q

What is esophageal manometry?

A

Esophageal manometry is a test used to measure the function of the lower esophageal sphincter (the valve that prevents reflux of gastric acid into the esophagus) and the muscles of the esophagus (see diagram). This test will tell your doctor if your esophagus is able to move food to your stomach normally

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12
Q

what is Zenker’s Diverticulum?

A

it is a consequence of esophageal dysmotility -> develop diverticulae

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13
Q

Where is the most common area for Zenker’s Diverticulum?

A
  • near pharynx
  • immediately above upper esophageal sphincter
  • Pulsion diverticulum
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14
Q

When do Zener’s Diverticulum usually occur?

A

after age 50

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15
Q

What are the clinical sx of Zener’s Diverticulum?

A

can be asymptomatic or store tons or food->mass,regurg,bad breath

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16
Q

where do diverticulum usually occur?

A

-diverticulum more common to occur right above the LES

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17
Q

Where does Traction diverticulum occur?

A

-mid-portion of esophagus

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18
Q

What diverticulum is associated with tuberculous lymph nodes

A

Traction diverticulum

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19
Q

What are the 2 types of pulsing diverticulum?

A

Zenker diverticulum

Epiphrenic diverticulum

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20
Q

Where does epiphrenic diverticulum occur?

A

immediately below lower esophageal sphincter

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21
Q

What is esophageal stenosis?

A

epithelial damage

  • fibrous thickening of submucosa
  • atrophy of muscular propria
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22
Q

what are causes of esophageal stenosis?

A

GERD,irradiation, or caustic injury –> inflammation and scarring

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23
Q

How does a patients weight fair in patients with esophageal stenosis?

A
  • patients keep weight nml and appetite nml

- (if the strictures are malignant will see weight loss)

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24
Q

What are esophageal mucosal webs?

A

semi circumferential eccentric

thin ledge-like protrusion of mucosa

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25
Q

where are esophageal mucosal webs usually seen?

A

most common in the upper esophagus

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26
Q

What diseases are associated with GERD, graft-versus-host disease, blistering skin disease?

A

esophagus mucosal webs

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27
Q

What are the clinical symptoms of esophageal mucosal webs?

A

non-progressive dysphagia if food is not chewed well

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28
Q

esophageal mucosal webs is a component of _________

A

plummer-vinson syndrome

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29
Q

what are the components of plummer vinson syndrome?

A
  • chronic iron deficiency anemia
  • upper esophageal web
  • atrophic glossitis
  • angular cheilitis (inflame of corners of the mouth)
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30
Q

what does plummer-vinson syndrome increase your risk for?

A

esophageal squamous cell carcinoma

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31
Q

what is the difference between rings and webs?

A
  • rings are similar to webs but are circumferential and thicker
  • they include the mucosa,submucosa, and in some cases hypertrophied muscularis
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32
Q

where would a “A” ring for esophageal ring (schatzki’s Ring)
located?

A

above GE junction

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33
Q

where would a “B” ring for esophageal ring (schatzki’s Ring) located?

A

if at the squamocolumnar junction

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34
Q

What is achalasia/ what are its triad features?

A

-cause of esophageal obstruction

Triad Features: 1. inability to relax LES 2. Increased LES tone 3. Absence of normal peristalsis

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35
Q

What are the clinical sx of achalasia?

A

solid and liquid dysphagia

-diff belching and chest pain

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36
Q

What is primary achalasia?

A
  • neurons/gangion cell degeneration (or nerves are not working properly)
  • idopathic (some familial)
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37
Q

how can you get secondary achalasia?

A

chugs disease (t. cruzi) destroys of myenteric plexus

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38
Q

What are DD of achalasia?

A
  • diabetic neuropathy
  • cancer
  • amyloidosis
  • sarcoidosis
  • down syndrome
  • remote herpes infection
  • sjogrens
  • Allgrove syndrome
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39
Q

what is allgrove syndrome?

A
  • achalasia
  • alacrima
  • adrenal insufficiency
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40
Q

how do you treat lap myomectomy?

A
  • lap myomectomy
  • ballon dilation
  • botox injection into LES
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41
Q

what is mallory-weiss tears?

A

-longitudinal laceration at GE junction

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42
Q

what is mallory-weiss tears caused by?

A
  • severe vomiting

- associated with severe alcoholism or bulimia

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43
Q

how does severe vomiting cause mallory-weiss tears?

A

-gastic contents cause wall to stretch and tear (bc no relaxation or contraction)

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44
Q

what is the prognosis of mallory-weiss tears?

A

usually heal rapidly and completely

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45
Q

what are the clinical symptoms of mallory-weiss?

A

hematemesis

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46
Q

what does malory-weiss increase the risk of?

A

Boerhaave syndrome

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47
Q

what is Boerhaave syndrome?

A

-transmural tearing and rupture of the distal esophagus

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48
Q

what can boerhaave syndrome lead to?

A

mediastinitis

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49
Q

what are the clinical syndromes of Boerhave syndrome?

A

severe chest pain

  • tachycardia
  • shock
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50
Q

what is the DD of Boerhave syndrome?

A

MI

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51
Q

how do you treat Boerhave syndrome?

A

surgery

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52
Q

which side is the tear on in mallory-weiss syndrome?

A

on the gastric side of the gastroesophageal junction

which may extend to the distal esophagus

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53
Q

what layers does mallory-weiss syndrome affect?

A

the mucosa and the submucosa

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54
Q

what layers des boerhaave’s syndrome effect?

A

complete rupture at the lower thoracic esophagus

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55
Q

In which syndrome do you see hammans sign?

A

boerhaaves syndrome

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56
Q

what is hammans sign?

A

crushing sound upon auscultation of the heart but due to pneumomediatstinum

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57
Q

which of the two syndromes boerhaave’s syndrome vs mallory-weiss syndrome gives you subcutaneous emphysema?

A

boerhaaves syndrome

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58
Q

what can cause esophageal varicies?

A
portal hypertension
#1-alcohol
#2-(world) schistosomiasis
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59
Q

what is the pathology of esophageal varies?

A
  • inflammatory erosion
  • venous pressure
  • increased hydrostatic pressure (associated with vomiting)
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60
Q

what population do you usually see esophageal varicose?

A

patients with cirrhosis?

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61
Q

what is the prognosis of esophageal varicose?

A

emergency
up to half die from first bleed
50% will bleed again w/in year

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62
Q

what do patients with esophageal varcies?

A

hypovolemic shock

hepatic coma

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63
Q

what is the clinical presentation of esophageal varies ?

A
  • clinically silent

- rupture with iller hematemesis

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64
Q

how do you treat esophageal varices?

A
  • sclerotherapy (inject thrombotic agents)
  • ballon tamponade
  • band ligation
  • PROPHYLACTICS: beta blockers and endoscopic vatical ligation
65
Q

what is chemical esophagitis caused by?

A
  • alcohol
  • heavy smoking
  • corrosive acids and alkalis-kids
  • pills
66
Q

what are the clinical sx of chemical esophagitis?

A
  • odynophagia (pain when swallowing)
  • bleeding
  • stricture
  • perforation
67
Q

what are the desquamative disorders associated with esophagitis?

A
  • pemphigus

- epidermolysis bullosa

68
Q

Where do you see infectious esophagitis?

A

-seen in immunosuppressed indiv
-Herpes
-cytomegalovirus
-candida
-Aspergillus
_mucormycosis

69
Q

how does herpes esophagitis px?

A

punched out ulcers

70
Q

what is the micro of herpes simplex esophagitis ?

A

-multinucleated squamous cells with herpes virus nuclear inclusions

71
Q

how does canidada Esophagitis px?

A

adherent gray-white pseduomemebranes composed of mated pseudohyphae

72
Q

How does eosinophilic esophagitis px micro?

A

large numbers more then 15 of intraepithelial eosinophils

73
Q

how does eosinophilic esophagitis px clinically?

A

adults-dysphagia

kids-GERD symptoms

74
Q

how does eosinophilic esophagitis occur?

A

may be allergic reaction against ingested food

75
Q

how do you treat eosinophilic esophagitis ?

A

avoid food allergens and steroids

76
Q

what is a major cause of esophagitis?

A

-reflux esophagitis aka GERD

77
Q

what gives you GERD/reflux esophagitis?

A

conditions that decrease LES tone or increases abdominal pressure

78
Q

what are the conditions that decrease LES tone or increases abdominal pressure leading to GERD

A
alcohol
tobacco
obesity
pregnancy
HIATAL HERNIA
CNS deppressants
delayed gastric emptying
increased gastric volume
79
Q

what are the clinical symptoms of GERD?

A
  • dyphagia
  • heart burn
  • sour gastric contents in mouth
  • rare: severe chest pain that mimics MI
80
Q

how do you treat GERD?

A

proton pump inhibitors (PPI)

H2blockers

81
Q

what is the micro of GERD?

A
  • basal cell hyperplasia
  • elongation of lamina propria papillae
  • eosinophils (scattered) and neutrophils in epithelial layer
82
Q

what is a hiatal hernia

A

protrusion of stomach into thorax

83
Q

what is a complication of hiatal hernia?

A

can cause LES incompetence

84
Q

what is barrett’s esophagus a complication of?

A

chronic GERD

85
Q

how does barrett’s esophagus look macro?

A

-red velvety mucosa extending up from GE junction

86
Q

describe the micro pathology of barrett’s esophagus

A

-squamous esophageal mucosa->intestinal metaplasia (columnar epithelium with goblet cells)

87
Q

what does barrett’s esophagus increase your risk of?

A

-increased risk of esophageal adenocarcinoma

88
Q

what is the most common benign tumor of the esophagus?

89
Q

what are the benign tumors of the esophagus

A
  • leiomyoma
  • fibroma
  • lipoma
  • hemangioma
  • neurofibroma
  • lymphangioma
90
Q

what are the most common malignant tumors of the esophagus?

A

-adeno carcinoma and squamous cell carcinoma are the most common

91
Q

what are the risk factors for adenocarcinoma of the esophagus?

A
  • # 1obesity related GERD and barrett’s esophagus

- tobacco use and radation

92
Q

what is protective against adenocarcinoma of the esophagus?

A
  • diets rich in fruits and veggies

- some types of H. pylori (gastric atrophy)

93
Q

is adenocarcinoma more common in men or women?

94
Q

what race is adenocarcinoma most common in?

95
Q

what is the strongest indicator of progression to adenocarcinoma?

A

degree of dysplasia

96
Q

what are the chromosomal abnormalities associated with adenocarcinoma

A

TP53 mutations

  • downreg of CDKN2A
  • downreg of p16/INK4 (early stage)
  • EGF,ERBWMET,cynclinD1 and E mutations (Late)
97
Q

what are the clinical sx of adenocarcinoma?

A

dysphagia

  • weight loss
  • hematemesis
  • chest pain
  • vomiting
98
Q

what is the prognosis of adenocarcinoma of the esophagus?

A

many have spread to the submucosal lymphatics at Dx

99
Q

what improves the prognosis of adenocarcinoma of the stomach?

A

if it is only in the mucosa and submucosa 80%

100
Q

what is the gross pathology of adenocarcinoma of the esophagus?

A
  • usually distal 1/3
  • can invade cardia of stomach
  • initially flat or raised patch
  • nodular mass or diffusely infiltrative or ulcerated
101
Q

what is the micro of adenocarcinoma of the esophagus?

A
  • usually mucin producing glandular tumors with intestinal features
  • rare: signet ring
  • rare: poor differentiation
102
Q

what age group do you see squamous cell carcinoma of the esophagus?

103
Q

which gender do you see a higher prevalence of squamous cell carcinoma of the esophagus?

104
Q

what are the risk factors for squamous cell carcinoma of the esophagus?

A
  • alcohol
  • tobacco
  • synergistic
  • caustic injury
  • achalasia
  • plummer-vinson syndrome
  • diet
  • papillomavirus
  • prior radiation (5-10 years before)
  • HPV
105
Q

plummer-vinson syndrome is a risk factor for?

A

squamous cell carcinoma of the esophagus

106
Q

what is the molecular basis for squamous cell carcinoma of the esophagus?

A
  • amplification for SOX2 gene (stem cell renewal)
  • over-expression of Cyclin D2
  • Loss of function mutations in TP53, e-cadherin and NOTCH1
107
Q

what are the sx of squamous cell carcinoma of the esophagus?

A
  • dysphagia
  • weight loss
  • hemorrhage
  • sepsis secondary to ulceration
  • tracheobronchial fistula with aspiration
108
Q

what race is squamous cell carcinoma of the esophagus most prevalent

A

african american

109
Q

iron deficiency anemia is associated with

A

squamous cell carcinoma of the esophagus

110
Q

what determines a poor prognosis for squamous cell carcinoma of the esophagus?

111
Q

what is a common way of death due to squamous cell carcinoma of the esophagus?

A

aspiration due to fistula

112
Q

where are squamous cell carcinoma of the esophagus usually seen?

A

mostly in mid 1/3 of esophagus

113
Q

how does the macro of squamous cell carcinoma of the esophagus look?

A

-grey-white lesions/plaques (early)->exophytic mass or cancerous ulceration or diffusely infiltrative neoplasm

114
Q

what can be a complication of squamous cell carcinoma of the esophagus if it invades the respiratory tree?

115
Q

what can be a complication of squamous cell carcinoma of the esophagus if it invades the aorta?

116
Q

what type of muscle is seen in the upper 1/3 of the esophagus?

117
Q

what type of muscle is seen in the lower 2/3 of the esophagus?

A

smooth muscle

118
Q

Is the esophagus relaxed or tonic during a swallow?

119
Q

is the esophagus relaxed or tonic at rest?

120
Q

what is the junction between the esophagus and the stomach?

A

squamo-columnar junction

121
Q

what foods increased LESp?

122
Q

what foods decrease LESp?

A

fats
chocolate
ethanol
peppermint

123
Q

what drugs decrease LESp?

A
Theophylline
ca-ch blockers
morphines
diazepam
serotonin
124
Q

what drugs increase LESp

A

histamine
antacids
pro-kinetics (memtoclopramid;doperidone)

125
Q

what is the intial test in diagnostic approach to dysphagia?

A

barium esophagram

126
Q

what type of disorders does barium esophagram evaluate?

A
  • structual lesions (stricture, web, haital hernia)

- at times GE reflux

127
Q

what esophageal diagnostic test directly visualized esophageal mucosa ad enables tissue diagnosis?

A

-endoscopy with biopsy

useful for hemostasis/dialation of strictures/stenosis

128
Q

what diagnostic test is useful for imaging lesions that are int he esophageal wall or immediately adjacent and good for staging esophageal malignancy?

A

endoscopic ultra sound

129
Q

what diagnostic test demonstrates reflex proper/amount and duration of reflux?

A

24 hour pH probe

130
Q

what esophageal manometry demonstrates tendency for GE reflux?

A

esophageal manometry

131
Q

what does esophageal manometry do?

A

measures pressures contractile activity and sphincter function

132
Q

esophageal manometry is useful for what type of disorders?

133
Q

what are the 2 different pathologies for GERD?

A

Aggressive(acid) vs defensive

134
Q

describe the defensive pathologies for GERD?

A

-anti-reflux barrier***most impt (LES-reduced resting pressure, TLESRs; increased abdominal pressures)
-esophageal acid clearance
(saliva, esophageal peristalsis, gastric emptying, intact esophageal mucosa, hiatal hernia)

135
Q

what is barrett’s metaplasia?

A

squamous epithelium changes to columnar epithelium

136
Q

what is the etiology of odynophagia

A

infectious
Candida
HSV
CMV

137
Q

if one has dysphagia with solid food only what type of disorder is this?

A

structural disorder

138
Q

if one has dysphagia with solid food only and it is progressive and rapid what is it?

A

structural disorder

carcinoma

139
Q

if one has dysphagia with solid food only and it is progressive and gradual with hx of GERD what is it?

A

structural disorder

peptic stricture

140
Q

if one has dysphagia with solid food only and it is intermittent what is it?

141
Q

if one has dysphagia with solids and liquids what type of disorder is it?

A

motility disorders

142
Q

if one has dysphagia with solids and liquids and is progressive with heartburn what is it?

A

scleroderma

143
Q

if one has dysphagia with solids and liquids and is progressive without heartburn what is it?

144
Q

if one has dysphagia with solids and liquids and is intermittent with chest pain what is it?

145
Q

what are the sx of zener’s diverticulum?

A

halitosis, dysphagia

regurgitation of undigested material

146
Q

what is the treatment of zenker’s diverticulum?

A
  • cervical myotome

- diverticulectomy

147
Q

what decade does achalasia px?

A

-presentation in 3rd to 5th decade

148
Q

how do you treat achalasia?

A

botox
pneumatic dilation
heller myotomy

149
Q

what causes pseudo-achalasia?

A
  • chagas’ disease (from T. cruzii)

- cancer for GE junction (more rapid onset, more weight loss)

150
Q

what is scleroderma?

A
  • connective tissue disorder

- replacement of smooth muscle with fibrosis (loss of LES function, poor esophageal peristalsis, result GE reflux)

151
Q

describe the manometry of scleroderma?

A
  • poor esophageal motility

- Low LESp

152
Q

what are the symptoms of diffuse esophageal spasm?

A

-chest pain or odynophagia or both

153
Q

what does the X-ray of diffuse esophageal spasm look like?

A

corkscrew esophagus

154
Q

what does the manometry of diffuse esophageal spasm look like?

A
  • simultaneous contractions
  • repetitive contractions
  • LES usually normal
155
Q

how do you treat diffuse esophageal spasm?

A
  • muscle relaxants
  • ca-ch blockers
  • nitrates
  • surgery
156
Q

what is the difference between the benign and malignant strictures?

A

benign-smooth

malignant-irregular

157
Q

what is caused by iron deficient anemia?

A

cervical webs

158
Q

what does the biopsy of esophageal mucosa show in eosinophilic esophagitis?

A

eosinophils>20HPF