GI Pathology: Small Intestine, Appendix, and Peritoneum Flashcards

1
Q

Describe the attached photo?

A

Small Intestine: Normal History

it is normal to have some lymphocytes & plasma cellsm in the lamina propria– it is not normal to have a lot

it is not normal to have PMNs in the epithelium

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2
Q

Describe the provided image?

A

Meckel Diverticulum

outpouching of the small intestine that contains all the layers of the small intestine wall

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3
Q

What is the “rule of twos” for meckel diverticulum?

A
  • about 2 inches in length
  • usually within 2 feet of ileocecal valve
  • Affect about 2% of the population
  • Two types of heterotopic tissues are commonly present
    • gastric
    • pancreatic
  • 2X more common in males than females
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4
Q

Identify the 4 major causes of intestinal ostruction

A
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5
Q

Identify the stucture in the following image?

A

Incarcerated Hernia

this is when the outpouching swells and it is impossible to get back in

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6
Q

Identify the stucture in the provided image

A

most common cause of obstruction in the united states

caused by intradominal inflammtion

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7
Q

What is an intussusception?

A
  • one segment of the intestine, constricted by a wave of peristalsis, suddenly becomes telescoped into the immediately distal segment of bowel
    • adults: tumors
    • kids: viral (adnovirus, rotavirus vaccine)
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8
Q

Identify the structure presented in the image?

A

Intussesception

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9
Q

Identify the structure presented in the image

A

Ischemic Bowel Disease: segmental infarction

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10
Q

identify the different types of ischemic bowel disease?

A

causes are going to be anything that causes obstruction of blood vessels

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11
Q

Identify the structure presented in the image?

A

Ischemic Bowel idsease: Global

any time there is a systemic problem of low fluid state

catastrophic event

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12
Q

The provided images are microscopic examples of what featue?

A

Ischemic bowel

heart attack of the bowel

organizing thormbus is the dark circular section

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13
Q

Describe neonatal necrotizing enterocolitis.

Most common demographic?

Pathogenesis?

Apearance?

A
  • demographics
    • premature
    • any part of small or large intestine
      • TI, cecum, right colon more common
  • pathogenesis
    • multi-factorial
      • genetic predisposition
      • immature GIT
      • initiation of oral feeding
      • bacterial colonization
      • intestinal ischemia
      • mucosal injury
    • x-ray: pneumonatosis intestinalis
    • gross: distended, grey-purple, gas bubbles
    • micro: ischemic necrosis, bacteria, gas bubbles
    • high perinatal mortality
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14
Q

What are the types of malabrosption syndromes?

Sympoms?

Common diseases?

A
  • Types (impaired absorption)
    • luminal brush border processing
    • absorption into intestinal mucosa
    • trasnport into circulation
  • symptoms
    • chronic diarrhea (relieved with fasting)
    • steatorrhea
    • flatulence
    • vitamin/mineral deficiencies
    • abdominla pain/ distension
    • muscle wasting
    • weight loss
  • dieseases
    • common in US
      • celiac disease (celiac sprue)
      • pancreatic insufficiency
      • chron disease
    • others
      • tropical sprue
      • whipple disease
      • cystic fibrosis
      • abetalipoproteinemia
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15
Q

Describe the antibody and cell mediated injury associated with celiac disease.

Histologic sequelae?

A
  • Antibody/cell mediated injury
    • Gluten is converted to Gliadin
      • gliadin induces IL-15 expression by epithelial cells
        • IL-15 activatees proliferation fo CD8+ T-cells in intestinal epithelium
        • epithelial damage
      • gliadin peptides leak into lamina propria and are deaminated by tissue trasnglutaminase and interact with HLA-DQ2 or DQ8 on APCs
        • APCs stimulate CD4+ T-cells to produce cytokines (contribute to tissue damage)
        • B-cell response with antibody production
  • Histologic sequelae
    • increased intraepithelial lymphocytes
    • villous blunting
    • crypt elongation
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16
Q

What is Celiac disease?

Demographic?

symptoms?

A
  • Immune-mediated enteropathy triggered by ingestion of gluten-containing foods in genetically predisposed individuals
  • Demographics
    • presents in infancy up to 30-60 years
    • typically caucasians of european descent
  • Symptoms
    • chronic diarrhea
    • bloating
    • fatigue
    • weight loss
    • failure to thrive (pediatric)
    • symptoms of malabsorption
    • asymptomatic
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17
Q

What is shown in the provided images?

A
18
Q

What are the criteria for diagnosis of celiac disease?

A
  • Clinical documentation malabsorption
  • small bowel biopsy – proven lesion
  • circulating disease related antibodies in serum
    • IgA against
      • antigliadin - sensitive
      • antiendomysial - sensitive & specific (difficult)
      • anti-tissue transglutaminase - sensitive & specific (easier)
      • anti-deamidated gliadin
    • if IgA deficient (more common in celiac patients)
      • anti-deaminated gliadin peptides IgG,
      • anti-TtG IgG (less sensitive and specific than Anti-DAG IgG)
  • uniequivocal improvemetn of sumptoms and mucosal histology on gluten withdrawl from diet
  • +/- HLADQ2 or HLADA8
19
Q

Celiac diseas is associated with what other heath indications?

A
  • IgA deficiency
  • other autoimune conditions (Type I DM)
  • Down syndrome
  • Dermatitis herpetiformis
  • Enteropathy associated T-cell lymphoma
  • Possibly higher incidence of small intestinal adenocarcinoma (controversial)
20
Q

What is the pruritic blisterin skin disorder seen in 10% of patients with celiac disease?

Why does this happen?

A

Dermatitis herpetiformis

  • seen in 10% patients with celiac disease
  • IgA antibodies cross react with epidermal tissue transglutaminase
  • subepidermal blister with neutrophilic microabcesses at tips of the dermal papillae
  • granular IgA on DIF
21
Q

What is shown in the provided images?

Person has Celiac disease

A

Agressive & rare

seen almost exclusively in patients with Celiac disease

22
Q

What is Tropical Sprue?

Where is is most common?

How is it treated?

A
  • histology similar to celiac diseases, except is worst in distal small bowel – etiologic agent is unknown
    • NO association with DH
    • NO significant risk of intestinal lymphoma or carcinoma
  • tropical climates
  • treat with broad-spectrum antibiotics
23
Q

What is whipple disease?

Etiological cause?

Symptoms?

A
  • Rare, systemic chronic disease
    • MF, 10:1
  • Caused by Tropheryma whippelii
  • Clinical symptoms
    • malabsorption, with diarrhea
    • lymphadenopathy
    • arthritis
    • +/- neuropsychiatric manifestations
  • Images
    • laminia propria is chalked full of stuff
    • with abundant clear cytoplastm– machrophages have engulfe organisms
24
Q

What is shown in the provided images?

A

seen almost exclusively with immunocompromised patients

25
Q

What are the different types of tumors of the small bowel?

A
  • Epithelial
    • adenomas- rare in small bowel
    • adenocarcinomas- rare in small bowel
  • Mesenchymal
    • GIST- uncommon in small bowel
    • leiomyomas and leiomyosarcomas
  • Lymphomas
    • MALT
      • most common SI lymphoma in Wesern countries
    • Enteropathy associated with T-cell lymphoma
      • celiad disease
    • Burkitt
      • ileum/ileocecal region
      • “starry-sky” pattern on histology
  • Neuroendocrine tumors (NET)- Most GI NETS arise in the small bowel
26
Q

Where do GI neuroendocrin tumors origniate from?

Range of classification?

Tumor products/composition?

A
  • Arise from GI mucosal endocrine cells
    • From well differentiated neuroendocrine tumors (G1, G2, G3) to reuroendocrine carcinomas (small cell carcinoma and large cell neuroendocrine carcinoma)
      • 1/3 SI tumors
  • Tumor products
    • gastrin
    • somatostatin
    • serotinin
      • urine metabolite: 5-hydroxyindolacetic acid
    • nothing/non-functional
  • Immunohistochemistry
    • positive: chromogranin, synaptophysin, CDX-2, various hormones
  • low grade malignant neoplasms
    • slow growth, but highly invasive
    • metastases
      • regional nodes, liver, bone, skin, viscera
27
Q

GI neuroendocrine tumor prognosis?

treatment?

A
  • prognosis
    • location is the most important prognostic factor
      • foregut (stomach, duodenum, esophagus)
        • rarely metastasize
      • midegut (jejunum ileum)
        • aggressive
      • hindgut (appendix, colorectal)
        • often an inciental finding & uncommonly metastasize
    • overall 5 years 50-65%
      • confined to SI wall- 85%
      • invasion of serosa- 5%
  • Treatment
    • wide surgical removal of primary tumor, regional nodes, isolated liver mets
28
Q

What are the clinical features of carcinoid syndrome?

What is it?

A
  • Caused by vasoactive substances secreted by tumor into systemic circulation
    • typically implies metastatic disease to liver
    • occurs in <10% patients with neuroendocrine tumors
  • Clinical features
    • skin: flushing, cyanosis, dermal sclerosis
    • GI: secretory diarrhea, abdominla cramps, nausea/vomiting
    • Cardiorespiratory: bronchoconstriction, right side valve fibrosclerosi, heart palpations, intermittent hypertension
  • Treatment
    • somatostatin analogue
29
Q

What is shown in the provided image?

A

classic neuorendocrine tumor

salt and pepper chromatin

30
Q

What is shown in the provided image?

A
31
Q

What is shown in the provided images?

A

Healthy appendix

32
Q

What is the difference between the two photos presented?

A

normal is very shiny serosal surface

appendicitis, serosa is rough & red & puffy

33
Q

What is shown in the provided images?

A

Acute appendicitis

need PMN in the gland

34
Q

What are the types of appendiceal tumors?

A
  • Well differentiated neuroendocrine (carcinoid) tumors
    • most common tumor of the appendix
    • often incidental and uncommonly metastasize
    • ofen occur and the tip of the appenxi
  • Mucinous Tumors of the appendix
    • may cause a “mucocele”
    • confined to appendix
      • Low grade amn
      • high grade amn
    • invasion of appendiceal wall is definitely demonstrated
      • mucinous adenocarcinoma
    • risk for pseudomyxoma peritonei
35
Q

What is shown in the provided image?

A
36
Q

What is shown in the provided images?

A
37
Q

What are the most common features of tumors of the peritoneum?

A
  • most are malignant
    • primary tumors are uncommon
      • mesothelioma
        • associated with asbestos exposure
    • secondary tumors are common
      • direct spread or metastatic seeding
  • Tumors metastatic to peritoneum
    • most common tumors producign diffuse serosal implants
      • ovarian carcinoma
      • pancreatic adenocarcinoma
    • mucinous carcinomas may produce pseudomyxoma peritonei
      • 95% arise from appendiceal mucinous tumors
      • 5% are of ovarian or pancreatic origin
38
Q

What is shown in the provied images?

A
39
Q

Describe the features of the primary peritonela mesothelioma

A
40
Q

What is shown in the provided images?

A

Pseudomyxoma peritonei