Histology of the SI & LI Flashcards

1
Q

What are plicae circulares and where are they found?

A

transverse folds w/ submucosal core

more visible in jejunum of SI

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2
Q

Intestinal villi

A

mucosal folds that project into lumen & cover surface of SI

simple columnar epi w/ enterocytes & goblet cells

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3
Q

Role of SI enterocytes

A

produce enzymes for digestion & absorption

found in epithelium

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4
Q

What glands are located in the submucosa of the duodenum?

A

Brunner’s glands

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5
Q

What is the function of Brunner’s glands?

A

Secretion of an alkaline fluid to neutralize acidic chyme.

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6
Q

Describe the 4 layers of SI

A

mucosa (simple columnar epi w/ enterocytes, GCs, & tubular glands)

submucosa (neurovasc, lymphatics & some glands)

muscularis (inner circular & outer longitud layers)

serosa (CT covered by visc peritoneum)

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7
Q

Innervation of SI/LI

A

motility controlled by ANS

peristalsis/contraction by submucosal plexus (of Meissner) & myenteric plexus of Auerbach

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8
Q

What is the structure of intestinal glands?

What cells compose intestinal glands?

A

simple tubular glands

enteroendocrine cells (secrete hormones)
Paneth cells
M cells
Intestinal stem cells

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9
Q

How many submucosal glands do we find in the jejunum?

A

The jejunum has no submucosal glands.

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10
Q

What do we call the lymphatic structure that assists with the absorption of fat in the intestinal villi?

A

Lacteal

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11
Q

Role of enteroendocrine cells

A

found thru out intestinal glands

secrete peptide hormones to control gut motility, regulate secretion of enzymes, HCl, bile & other components for digestion

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12
Q

Location & function of paneth cells

A

pyramidal shaped cells @ base of intestinal glands (super pink in color b/c lots of secretory granules)

function in innate immunity by secreting anti-microbial substances (lysozymes & alpha defensins) & regulate normal bacterial flora

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13
Q

What is the role of M (microfold cells)?

A

function as highly specialized antigen-transporting cells in ileal mucosa (overlying Peyer patches)

bind macromolecules & bacteria (E coli) to internalize them & transfer to immune cells

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14
Q

Histologically speaking, where are intestinal glands found?

A

Throughout the mucosal layer of the entire small intestine

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15
Q

Describe the histology of the gastroduodenal junction

A

stomach will have thick muscle wall b/c pyloric sphincter muscle & pyloric glands @ base of each gastric pit

duodenum will have many Brunner’s glands in submucosa (deep to muscularis mucosae)

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16
Q

Hallmarks of duodenum

Role of duodenum

A

Brunner’s glands in submucosa (to neutralize acidic chyme)

collect bile & pancreatic secretions via hepatopancreatic ampulla

17
Q

Hallmarks of jejunum

A

long finger-like villi (tubular intestinal glands & villus w/ lacteals)

NO submucosal glands

lymph nodules in lamina propria

18
Q

Hallmarks of ileum

A

shorter finger-like villi

Peyer’s patches (muscoal lymphoid nodules specific to ileum)

some paneth cells @ base of glands

19
Q

Histology of ileocecal junction

A

abrupt transition from villi of SI to glandular epithelium of LI

thickened muscularis

20
Q

Why is the valve @ the ileocecal junction thick?

A

thickened extension of muscularis mucosae that limits reflux of colonic contents into ileum

21
Q

Hallmarks of LI

A

GOBLET CELLS
NO intestinal villi
muscoa w/ tubular intestinal glands

22
Q

Why does the LI have goblet cells?

A

GC produce lots of mucus needed to move hard, solid waste thru tube

23
Q

What do we call the simple columnar cells of the large intestine epithelium?

A

Colonocytes

24
Q

What layer, in the colon, forms the tinea coli?

A

The outer longitudinal layer of the muscularis externae

form haustra of LI

25
Q

Why would the GALT of the LI be extensive?

A

b/c gut is exposed to external environment

26
Q

What is the basic pathophysiology of Hirschsprung’s disease?

A

Neural crest cells fail to differentiate causing an absence of both plexuses in the colon or bowel segment. This results in absent peristalsis, and leads to megacolon through impactions.

27
Q

Hirschsprung’s disease presentation, diagnosis & treatment

A

present w/ constipation, poor feeding & progressive ab distension

diagnosed w/ delayed BM<48hrs after birth, rectal biopsy

treatment by removing affect colon segment & pulling through ganglionic colon segments that are properly innervated

28
Q

What is the most common type of Hirschsprung’s disease?

A

“Short segment disease” – where the issue is confined to the “rectosigmoid region” (rectum and sigmoid colon).

29
Q

What are the three divisions of the anal canal?

A

The colorectal zone, the anal transitional zone, and the squamous zone.

30
Q

Where does the enteric nervous system end?

A

At the anal transitional zone of the anal canal

31
Q

Describe histology of the rectum (upper part)

A

typical muscoa w/ tubular intestinal glands & transverse rectal folds

32
Q

Where are circumanal glands found?

A

large apocrine glands (release of apical portion of cell) surrounding anal orifice

33
Q

When can you see anal sinuses?

A

when bowel is empty

34
Q

Where are anal glands found?

A

Extending into the submucosa and muscularis externa of the anal canal

35
Q

What are the anal columns formed from?

A

Mucosal folds of the anal canal

36
Q

Describe different zones of anal canal

A

colorectal zone-simple columnar epi

anal transitional zone-simple columnar & stratified squamous

squamous zone-stratified squamous epi (blending w/ peri-anal skin)