GI/Alimentary Canal Histology Flashcards

1
Q

esophagus

A

-muscular tube
-connecting the pharynx and stomach
-function: moves food from pharynx to stomach by peristalsis

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2
Q

layers of the esophagus

A

from lumen down:
-adventitia- serosa is absent in the cervical and mediastinal esophagus —> loose and weak connective tissue
-muscularis propria- two layers of an inner circular muscular layer and an outer longitudinal muscle layer
-submucosa- loose connective tissue and the thick submucosa layer is the strongest layer of the esophagus
-mucosa- innermost layer of the esophagus —> thick, nonkeratinized (soft), stratified squamous epithelium that is a continuation of the oropharyngeeal mucosa

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3
Q

what do the salivary enzymes do?

A

-convert food into a mass called foot bolus
-once the food bolus reaches the pharynx —> swallowing starts and relaxation of the upper esophageal sphincter ensues to allow passage of food bolus into the esophagus —> bolus then travels down the esophageal body aided by peristaltic contractions of the esophageal mucles —> when it finally reaches the distal end of the esophageal body, it triggers relaxation of the lower esophageal sphincter and permits entry of the food bolus into the stomach

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4
Q

lower esophageal sphincter

A

-not an anatomical sphincter —> no well defined thickening or muscle that controls it
-considered a physiological or functional sphincter
-when it is not functioning properly, it can cause gastric acid reflux from the stomach into the LES and this can cause heart burn

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5
Q

esophagus mucosa

A

-3 layers: epithelium, lamina propria, muscularis mucosa
-lower esophageal sphincter is not an anatomical sphincter

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6
Q

esophagus submucosa

A

-contains fibroblasts, elastin fibers (allow esophagus to expand when food passes through), sparse ganglia (meissner plexus), lymphatic channels, blood vessels, and submucosal glands
-submucosal glands are comprised of mucinous cells surrounding a central lumen that produces acid mucin —> found only in the esophagus and duodenum (helps lubricate the surface of the esophagus)

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7
Q

muscularis propria

A

-composed of striated skeletal muscle and smooth muscle
-skeletal muscle in the proximal esophagus (voluntary control)
-smooth muscle in the distal esophagus
-inner layers orient circumferentially whereas the outer layers orient longitudinally to allow for segmental contraction and peristalsis
-myenteric plexuses (nerves and ganglia) found between inner and outer layers —> produce rhythmic contraction to result in parastaltic movement of the esophagus

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8
Q

adventitia

A

-outermost layer
-loose irregulat connective tissue
-function: connect esophagus to external structures (retroperitoneal organs)
-serosa is the last 1-2 cm of the esophagus and within the abdominal cavity below the diaphragm —> composed of simple squamous epithelium or mesothelium and it is continuous with the abdominal mesenteris

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9
Q

pits and glands of the stomach

A

-cardiac, fundic, and pyloric regions of the stomach contain different arrangements of gastric pits/glands
-smooth lining of the gut is columnar epithelial cells (mucuous cells) and the lining is punctured by gastric pits with tubular glands emptying into pits
-gastric fluid or digestive enzymes/HCl are produced within these glands depending on the region
-gastric pits are mucuous cells that are uniform throughout
-gastric glands are secretory/endocrine cells

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10
Q

cardiac region

A

-narrow circular region at gastrointestinal junction
-contains short pits with mucosal-secreting cardiac glands
-pits are coiled tubular glands producing thick mucous cells that are simple columnar
-mucous made of alkaline to protect adjacent esophageal mucosa from stomach acid secretions
-thin layer of mucosa and reduced number of gastric pits/glands

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11
Q

fundic region

A

-projects into dome-like structure above esophagus forming largest and central region of the stomach
-contains gastric pits/glands that produce gastric digestive enzymes/HCl to digest foods
-thicker layer of gastric pits and glands have smaller lumens

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12
Q

pyloric region

A

-funnel-shape opening up into the pyloric sphincter
-contains long pits and mucous-secreting glands
-deeper pits and shorter glands that produce gastrin hormone

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13
Q

parietal cells

A

-facilitate digestions through secretions
-secrete gastric acid or HCl, which will activate gastric enzymes and kill bacteria
-intrinsic factor is required for B12 absorption —> important for a variety of cellular processes
-“fried egg” appearance with a central nucleus and eosinophilic cytoplasm

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14
Q

chief cells

A

-work in conjunction with parietal cells to induce digestive activity
-produce a protein called pepsinogen –> at a normal pH, it is completely inactive but upon HCl secretion, it increases acidity and is activated into pepsin, proteolytic enzyme within the stomach liquid —> processes digested proteins since the pepsin can break down the proteins into polypeptides
-secrete lipase which breaks down fats
-secrete leptin which controls signals for food intake and energy expenditure
-eccentric nuclei with more blue/purple cytoplasm

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15
Q

enteroendocrine cells (G cells)

A

-provide important role in controlling digestion
-works with nervous system to initiate digestive actions
-secretes gastrin, which induces HCl production in parietal cells
-located near the base of glands in the stomach
-inconspicuous appearance with H&E, commonly IDed with immunohistochemistry

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16
Q

three parts to the small intestine

A
  1. duodenum
  2. jenjunum
  3. illeum
    function of the small intestine: absorb nutrients
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17
Q

duodenum

A

-adjusts pH, tonicity
-distinguishing features are flatter villi, brunner’s glands in the submucosa

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18
Q

jejunum

A

-digests and absorbs
-distinguishing feature is the paneth cells, which are secretory glands between villi and within crypts of lieberkuhn

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19
Q

illeum

A

-absorbs bile salts
-distinguishing feature of shorter villi and peyer’s patch in the submucosa

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20
Q

features of the large intestine/colon

A

-cecum —> ascending colon —> transverse colon —> descending colon —> sigmoid colon
-involved in fluid absorption

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21
Q

large intestine

A

-increased goblet cells to produce mucus for easy passage
-crypts instead of villi
-made up of the mucosa, submucosa and muscularis propria

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22
Q

structural unit of the intestines

A

-villi are lined by simple columnar epithelium
-evaginations of mucosa in finger-like projections
-function to increase surface area for absorption and allow for secretion of substances by specialized cell types

23
Q

layers of the GI tract

A

-mucosa is the innermost layer with direct contact with food
-submucosa is made up of connective tissue with blood vessels, nerves, and lymphatics
-muscularis has smooth muscle with the inner being circular and the outer longitudinal
-serosa is the outermost layer with smooth muscle

24
Q

intestines- peristalsis

A

-muscularis propria has longitudinal layer made up of smooth muscle and circular layer
-circular layer contracts to propel the chyme forward
-longitudinal layer contracts to shorten the small intestine
-circular layer contracts
-contraction and relaxation of the muscularis propria allows the bolus to move through the small intestine

25
Q

brunner’s glands

A

-distinguishing feature of the duodenum
-found in the submucosa of the duodenum
-compound tubular glands that secrete alkaline mucus (rich in HCO3) to neutralize acidic chyme from the stomach

26
Q

peyer’s patches

A

-distinguishing feature of the illeum
-large aggregations of lymphoid follicles in the lamina propria and submucosa of the illeum
-specialized epithelial cells called M cells that cover peyer’s patches and their apical microfolds uptake particles, microorganisms, and transport antigens to lymphatic tissues

27
Q

paneth cells

A

-specialized intestinal columnar cells
-located at the basal portion of the intestinal glands (crypts)
-exocrine cells with large, eosinophilic secretory granules
-provide protective function through granule release of defensins, lactoferrin, and lysozymes

28
Q

auerbach’s and meissner’s nerve plexus —> innervation of the GI tract

A

-enteric nervous system- autonomic neurons organized into small ganglia in the submucosa and muscularis externa of the GI tract
-meissner’s submucosal plexus controls activity of glands and smooth muscle in the mucosa
-auerbach’s myenteric plexus controls peristalsis, the activity of the muscularis externa

29
Q

esophageal-gastric junction

A

-located in the meeting point between esophagus and the stomach (cardiac region)
-stratified squamous non-keratinized epithelium (esophageal) to mucinous simple columnar epithelium (gastric)
-lose submucosal esophageal glands and gain gastric oxyntic glands
-prevents food and stomach acid from retrograding

30
Q

recto-anal junction

A

-bend in the GI tract where the rectum meets the anus
-combo of internal and external sphincters with the puborectalis muscle
-simple columnar (colon) to stratified squamous (skin)
-prevents passage of fecal material

31
Q

pyloric region

A

-distal portion of the stomach that opens into the small intestine at the sphincter
-long pits and pyloric glands
-valve that allows passage of food to the small intestine

32
Q

appendix

A

-appendage to the cecum
-similar structure to the large intestine except with smaller lumen and lower density of glands
-many lymphoid follicles in mucosa/submucosa
-no known function

33
Q

duodenum

A

-pylorus of stomach to the duodenojejunal junction
-initial segments of the small intestine and retroperitoneal
-brunner’s glands in the submucosa with alkaline mucous and urogastrone
-absorbs iron

34
Q

illeum

A

-distally to the jejunum and connected to the cecum —> distal segment of the small intestine
-peyer’s patchs in the lamina propria
-absorbs B12 and bile salts plus produces mucin

35
Q

what composes villi of the small intestine?

A

capillaries and lacteals

36
Q

barrett’s esophagus

A

-condition involving damage to the inner lining of the esophagus
-does not cause symptoms
-associated with GERD, where the stomach contents, especially the acid, reflux into the esophagus leading to heartburn, indigestion, and nocturnal regurgitation
-diagnosis is through an upper endoscopy and biopsy —> BE has salmon pink color compared to normal white color

37
Q

BE pathophysiology

A

-acid escapes from stomach to the lower part of the esophagus
-acid damages normal inner lining of the esophagus
-squamous cells are replaced by columnar goblet cells (intestinal cells) —> intestinal metaplasia
-goblet cells are more resistant to stomach acid

38
Q

BE histology

A

-esophageal stratified squamous epithelium is replaced by intestinal columnar epithelium with goblet cells

39
Q

BE vs chronic bronchitis

A

-BE: intestinal metaplasia with stratified squamous epithelium —> columnar intestinal metaplasia
-CB: squamous metaplasia with pseudostratified columnar epithelium —> squamous metaplasia

40
Q

lacteals

A

-exclusively present in the small intestine
-located centrally in the villi within the lamina propria
-play a role in absorbing dietary fats and fat soluble vitamins
-once in the lacteals, fats —> lymphatic system —> bloodstream
-they also a play a role in the gut immune response by facilitating the transport of antigen and antigen presenting cells

41
Q

primary intestinal lymphangiectasia (PIL)

A

-waldmann disease
-rare congenital disorder with no known cause
-mainly characterized by edema —> enlarged lacteals leading to disrupted absorption and leaking of lymph fluid back into the intestine

42
Q

symptoms of intestinal lymphangiectasia

A

-nutrient deficiencies
-protein loss (albumin) so decreased oncotic pressure
-edema (primarily in limbs)
-abdominal discomfort with swelling of the pericardium and fluid in the chest

43
Q

secondary intestinal lymphangiectasia

A

-due to underlying conditions that block of damage lymphatic vesels in the intestines
-cancers or tumors, inflammatory diseases like crohn’s, and trauma or lymphatic infections like whipple’s disease or TB

44
Q

treatments of lymphangiectasia

A

-strict long term low fat diet
-diuretics
-albumin infusion leading to increase of oncotic pressure
-removal of diseased portion of intestine if localized
-secondary intestinal lymphangiectasia will be treated by addressing the primary cause of lymphatic obstruction

45
Q

colon

A

-absorbs water and electrolytes
-produces mucus lubricating intestinal surface
-divided into four layers: mucosa, submucosa, muscularis propria, and serosa

46
Q

hirschsprung

A

-motor disorder of the colon with missing nerve cells causing problems passing stool
-congenital defect
-mostly occurs with newborn infants who have not had a bowel movement in the first 48 hours after birth
-diagnosed via rectal biopsy

47
Q

hirschsprung pathophysiology

A

-aganglionosis- absence of enteric ganglion cells in the submucosal and/or myenteric nerve plexus of colon
-motor disorder caused by failure of neural crest cells to migrate during intestinal development of fetal life
-aganglionic segment of the colon fails to relax causing a functional obstruction
-intestinal contents build up behind the obstruction/blockage

48
Q

hirschsprung histology

A

-aganglionic segment with absence of submucosal and myenteric ganglion cells
-submucosal and myenteric nerve enlargement

49
Q

colonic adenocarcinoma

A

-cancer of the epithelial cells from colonic mucosa
-third most commonly diagnosed and cause of cancer-related death in the US
-most common cancer of the GI tract
-risks include age, family history, genetic predisposition, illnesses like IBD, alcohol, smoking, obesity

50
Q

symptoms of colonic adenocarcinoma

A

-rectal bleeding
-abdominal pain
-anemia
-diagnosed with colonoscopy, barium enema, and CT colonoscopy

51
Q

pathophysiology of colonic adenocarcinoma

A

-accumulation of multiple genetic mutations over time
-three major pathways: ICN (APC (tumor suppression) mutations), microsatellite instability (DNA mismatch repair (MMR) mutations like MLH1, MSH2), and CpG island hypermethylation (CIMP) (BRAF (oncogene) mutations and leads to serrated polyps)
-mutations are largely acquired sporadically but ~3-5% have well defined inherited mutations with lynch syndrome (germline mutations in the MMR genes) and familial adenomatous poylposis (FAP) with germline mutations of the APC genes

52
Q

colon cancer histology

A

-healthy colon mucosa: formation of glands with a regular pattern
-in adenocarcinoma, fewer glands and irregular pattern and structure
-colonic adenocarcinoma is typically graded by level of glandular formation —> well differentiated (>95% of tumor gland-forming), moderately differentiated (>50%), and poorly differentiated (<50%)

53
Q

colonic adenocarcinoma treatments

A

-surgery
-chemotherapy
-immunotherapy, which is really good for microsatellite instability