Clinical Medicine of Gastrointestinal System: Oral Manifestations of the GI Disease and Diseases of the GI Tract, pt.1

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51 Terms

1
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Why are there oropharyngeal presentations of the GI Tract disease?

b/c the oral cavity is the window of the gut

2
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aphthous stomatitis

ulcers = canker sores

-solitary or multiple

-RAS = recurrent aphthous stomatitis

-associated with crohn's disease **

<p>ulcers = canker sores</p><p>-solitary or multiple</p><p>-RAS = recurrent aphthous stomatitis</p><p>-associated with crohn's disease **</p>
3
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What are the predisposing factors for aphthous stomatis?

-stress

-viral illness

-hormonal changes

-food/drug hypsersenstivity

-familial

-trauma

-immunodeficiency

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What is the likely etiology for aphthous stomatitis?

immune response

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What are the GI diseases associated with aphthous stomatitis?

-crohn's disease --> aph ulcerations throughout the GI tract

-iron deficiency anemia --> multiple GI and non-GI etiologies

-celiac disease (less common)

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cheilitis

inflammation of the lips

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angular cheilitis

dryness at the corners of the mouth leading to skin breakdown, redness, crusting, & fissures

*may become infected

<p>dryness at the corners of the mouth leading to skin breakdown, redness, crusting, &amp; fissures</p><p>*may become infected</p>
8
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What are common causes of angular cheilitis?

-irritation--> chemical, dry mouth, poor fitting dentures, edentualism

-iron deficiency, riboflavin deficiency, poor nutrition

-infection

-allergies

-decreased immune function

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How does edentualism (of having lost one or more teeth, whether partially or fully) cause angular cheilitis?

leads to more saliva exposure at the corners of the mouth --> repetitive exposure to saliva leads to skin breakdown = form of contact dermatitis

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Peutz-Jeghers Syndrome

mucocutaneous hyperpigmentation that presents as pigmented macules on lips and buccal mucosa

-autosomal dominant

-presents in 1st-3rd decade

-can fade after puberty

-can also have lesions on fingers, soles, & around the eyes

-associated with polyps of the GI tract **

-risk for multiple cancers

<p>mucocutaneous hyperpigmentation that presents as pigmented macules on lips and buccal mucosa</p><p>-autosomal dominant</p><p>-presents in 1st-3rd decade</p><p>-can fade after puberty</p><p>-can also have lesions on fingers, soles, &amp; around the eyes</p><p>-associated with polyps of the GI tract **</p><p>-risk for multiple cancers</p>
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What GI disorder is Peutz Syndrome associated with?

hamartomatous Peutz-Jeghers Polyps (PJPs) --> associated with multiple polyps of GI tract

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Peutz Syndrome increases the risk for which cancers?

-38-66% risk GI cancer --> stomach, small intestine, colon, pancreas

-increased risk for lung, breast, ovarian/testicular

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What are the complications of the GI polyps that are associated with Peutz Syndrome?

-intestinal onstruction

-abdominal pain

-GI bleeding

-malignant transformation

-rectal prolapse

14
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Mucocutaneous Telangiectasia/Hereditary Hemorrhagic Telangiectasia

vascular malformation of the skin and internal organs (GI tract, lungs, brain) ==> AKA Osler-Weber-Rendu Syndrome

-presents in 2nd or 3rd decade

-autosomal dominant

<p>vascular malformation of the skin and internal organs (GI tract, lungs, brain) ==&gt; AKA Osler-Weber-Rendu Syndrome</p><p>-presents in 2nd or 3rd decade</p><p>-autosomal dominant</p>
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Telangiectasia

small, dilated blood vessel near surface of skin/mucous membranes.

*common on lips, tongue, face, chest, fingers, GI tract

<p>small, dilated blood vessel near surface of skin/mucous membranes.</p><p>*common on lips, tongue, face, chest, fingers, GI tract</p>
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Hereditary hemorrhagic telangiectasia?

-telangiectasia --> small, dilated blood vessel near surface of skin/mucous membranes (lips, tongue, face, chest, fingers, GI tract)

-Arteriovenous shunts/malformations (AVMs) --> Liver (60%), brain (10%), respiratory system

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What are the complications of hereditary hemorrhagic telangiectasia?

-epistaxis --> nosebleeds (97%)

-GI bleeding (33%)

-iron deficiency

-stroke

-pulmonary hemorrhage/embolism

18
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oral candidiasis

oral mucocutaneous candida infection = oral thrush --> fungal infection, can be chronic or acute; local or systemic

*presents as creamy white/yellow curd like plaques on the tongue/oral mucosa

-often asymptomatic

-symptoms --> "cotton mouth", loss of taste, odynophagia

-can accompany esophageal candidasis

<p>oral mucocutaneous candida infection = oral thrush --&gt; fungal infection, can be chronic or acute; local or systemic</p><p>*presents as creamy white/yellow curd like plaques on the tongue/oral mucosa</p><p>-often asymptomatic</p><p>-symptoms --&gt; "cotton mouth", loss of taste, odynophagia</p><p>-can accompany esophageal candidasis</p>
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How is oral candidiasis diagnosed?

-clinical

-yeast seen on smear

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What underlying conditions associated with oral candidiasis?

-diabetes

-HIV/AIDS

-cancer

-medications --> chemotherapy, steroids, antibiotics

-smoking

-other immunocompromised states

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How is oral candidasis related to underlying GI disease?

seen when GI diseases are treated with steroids in advanced GI cancer or chemotherapy for GI cancers

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hyperdontia

supernumerary teeth ==> extra permanent teeth (1-4% of population)

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What diseases are associated with hyperdontia?

-cleidocranial dysplasia

-ehlers-danlos syndrome

-cleft lip and palate

-gardner syndrome

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Garner Syndrome

-autosomal dominant

-supernumerary teeth

-osteomas

-odontomas

-many colon polyps w/ 100% chance of malignant change--> variant of familial adenomatous polyposis

-colon cancer at 20-40 years old without treatment

<p>-autosomal dominant</p><p>-supernumerary teeth</p><p>-osteomas</p><p>-odontomas</p><p>-many colon polyps w/ 100% chance of malignant change--&gt; variant of familial adenomatous polyposis</p><p>-colon cancer at 20-40 years old without treatment</p>
25
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What are signs of anemia in the mouth?

-angular cheilitis

-atrophic glossitis

-RAS like ulcerations

-oral lichen planus

-xerostomia

-numbness

-burning sensation

-dysgeusia--> altered taste perception

<p>-angular cheilitis</p><p>-atrophic glossitis</p><p>-RAS like ulcerations</p><p>-oral lichen planus</p><p>-xerostomia</p><p>-numbness</p><p>-burning sensation</p><p>-dysgeusia--&gt; altered taste perception</p>
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dysgeusia

altered taste perception

27
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How does the signs of anemia in the mouth relate to the GI?

many GI disorders are associated with anemia due to malabsorption or blood loss

28
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crohn's disease

inflammatory bowel disease characterized by bouts of abdominal pain, diarrhea, weight loss, nutritional deficiencies due to lesions anywhere in the GI tract-- including the oral cavity

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What are the oral manifestations of crohn's disease?

-cobble-stone appearance (specific to crohn's)

-linear ulceration

-mucosal tags

-mucositis & gingivitis

-labial & facial swelling

-angular cheilits

-aphthous ulcers

<p>-cobble-stone appearance (specific to crohn's)</p><p>-linear ulceration</p><p>-mucosal tags</p><p>-mucositis &amp; gingivitis</p><p>-labial &amp; facial swelling</p><p>-angular cheilits</p><p>-aphthous ulcers</p>
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What are the signs & symptoms of crohn's disease?

-chronic abdominal pain

-diarrhea--> 70% bloody, 30% non-bloody

-weight loss

-extra-intestinal manifestations

-onset around 15-25, but can be later

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Describe the pathology of crohn's disease.

-transmural inflammation of bowel wall

-can affect anywhere in the GI tract--> most commonly includes the ileum

-lesions tend to spare the rectum & skip segments of GI tract

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What would you expect to see in an endoscopy of a patient with crohn's disease?

cobblestone appearance w/ linear ulceration (discontinuous)

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What are the common complications of crohn's disease?

-intestinal obstruction

-fistulas

<p>-intestinal obstruction</p><p>-fistulas</p>
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What are some common treatments of crohn's disease?

-steroids & other meds to modify disease

-surgery for bowel obstruction

35
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ulcerative colitis

inflammatory bowel disease characterized by bouts of bloody diarrhea

-often bloody mucosal ulceration of the colon.

-anemia common

-oral manifestations

>pyostomatis vegetans--> low occurence but more common here than in crohn's disease

>RAS-like ulceration

>angular cheilitis

>atrophic glossitis

>other anemia findings

<p>inflammatory bowel disease characterized by bouts of bloody diarrhea</p><p>-often bloody mucosal ulceration of the colon.</p><p>-anemia common</p><p>-oral manifestations</p><p>&gt;pyostomatis vegetans--&gt; low occurence but more common here than in crohn's disease</p><p>&gt;RAS-like ulceration</p><p>&gt;angular cheilitis</p><p>&gt;atrophic glossitis</p><p>&gt;other anemia findings</p>
36
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What are the oral manifestations of ulcerative colitis?

-pyostomatitis vegetans --> erythema, edema, & pustules of gingiva (low occurrence but more likely here than in crohn's)

-RAS-like ulceration

-angular cheilitis

-atrophic glossitis

-other anemia findings

<p>-pyostomatitis vegetans --&gt; erythema, edema, &amp; pustules of gingiva (low occurrence but more likely here than in crohn's)</p><p>-RAS-like ulceration</p><p>-angular cheilitis</p><p>-atrophic glossitis</p><p>-other anemia findings</p>
37
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What are the signs and symptoms of ulcerative colitis?

-fever

-abdominal pain

-bloody diarrhea --> can be nocturnal

-extra-intestinal manifestations --> skin & joints

-signs of anemia

-onset 15-25 years old (can be later)

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what is the pathology/endoscopy of ulcerative colitis?

continuous mucosal inflammation & ulceration of the colon

<p>continuous mucosal inflammation &amp; ulceration of the colon</p>
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What are common treatments of ulcerative colitis?

-total colectomy can be curative

-medications to modify disease, including steroids

40
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celiac disease

gluten sensitive enteropathy==> immune-mediated disease w/ diverse presentation

-oral manifestations may be a early sign in childhood or the only sign

>enamel defects--> hypoplasia w/ discoloration & banding

>aphthous ulcers

-severe disease can lead to malnutrition through malabsorption

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What are the oral manifestation of celiac disease?

-enamel defects --> hypoplasia w/ discoloration & banding

-aphthous ulcers

<p>-enamel defects --&gt; hypoplasia w/ discoloration &amp; banding</p><p>-aphthous ulcers</p>
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What are the consequences of severe celiac disease?

-malnutrition thru malabsorption

-multiple deficiencies --> Ca2+, vitamin D, vitamin K, vitamin B12

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What are the symptoms of Celiac Disease?

-abdominal pain

-bloating

-weight loss

-chronic diarrhea

-steatorrhea

-extra-intestinal manifestations

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What is the pathology of celiac disease?

blunting of intestinal villi & inflammation

*common in duodenum

<p>blunting of intestinal villi &amp; inflammation</p><p>*common in duodenum</p>
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How is celiac disease diagnosed?

labs

-antibodies for tissue transglutaminase antigens

-antibodies to other specific antigens

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Treatment of Celiac Disease

-gluten-free diet

-nutritional supplementation for any deficiencies

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Gastroesophageal Reflux Disease (GERD)

reflux severe enough to cause symptoms and/or tissue injury ==> causes reflux esophagitis

<p>reflux severe enough to cause symptoms and/or tissue injury ==&gt; causes reflux esophagitis</p>
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What are the predisposing factors of GERD?

-hiatial hernia

-obesity

-delayed gastric emptying

-diet

-medications

-lifestyle

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What are all complications of GERD?

-developing a sour taste in the mouth

-bad breath --> due to slight regurg of acidic foods

-pain or swelling in the throat

-dysphagia

-hoarseness

-stomach noises

-nausea & loss of appetite

-dry mouth

-gum irritation including bleeding & tenderness

-tooth erosion

-heartburn behind breastbone after meal

-bloating, burping, or passing gas after meals

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What are some key complications of GERD?

-severe dental disease

-esophageal ulceration

-esophageal stricture

-metaplasia to Barret's Esophagus

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Treatment of GERD

-lifestyle changes

-OTC meds --> acid neutralizers, PPIs, H2 blockers