UWORLD GI Flashcards

1
Q

Tx pregnancy and gallstones

A

Asymptomatic: no treatment.
pregnancy-related gallstones resolve spontaneously within 2 months of delivery.

Symptomatic treated with IV fluids and pain control. if persistent: cholecystectomy during the second trimester.

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2
Q

Anal Abscess Sxs

A

severe, constant pain
fever or malaise.

PE: Erythematous, indurated skin or a fluctuant mass over the perianal or ischiorectal space.possibly Purulent drainage

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3
Q

Anal Abscess Tx

A

Most important: prompt incision and drainage (I&D) of the abscess

Oral antibiotics for pt with DMs, immunosuppression, extensive cellulitis, or valvular heart disease. Abx after I&D

Admit not necessary for localized infection

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4
Q

Anal abscess vs fistula

A

Anal abscess is an infection within one or more of the anal spaces

Anal fistula is a tunneling between the anus or rectum and another epithelial lined space (eg, the skin overlying the drainage site).

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5
Q

Anal fistula SXS and Tx

A

Typically present with an anal abscess that persists or with a pustule-like lesion in the perianal or ischiorectal area that continually drains.

Surgical repair is usually necessary to eliminate the fistula while preserving fecal continence.

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6
Q

GERD vs H. Pylori infection

A

Helicobacter pylori presentas as dyspepsia ( epigastric burning and symptoms of bloating, nausea, or early satiety)

GERD- substernal burning and regurgitation, sour taste

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7
Q

Drug induced pancreatitis

“Daily” drugs

A

Antihypertensive: thiazides, furosemide, enalapril, losartan

Antiepileptic: valproate acids, carbamazepine

Immunosuppressants: azathioprine, mercaptopurine, corticosteroids

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8
Q

Drug Induced Pancreatitis

“Occasional/ event” drugs

A

Antibiotics: Isoniazid, Tetracyclins, metronidazole, TMP-SMX

Antivirals: lamivudine, didanosine

Analgesics: NSAID, Acetaminophen, Pilates, mesalamine, sulfasalazine

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9
Q

Mechanism of Drug induced pancreatitis

A

-Hypersensitivity sulfonamide
-Ischemia due to decreases intravascular volume
-Increased viscosity of pancreatic secretions

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10
Q

White by baccal lesions that can be scrapped of leaving hyperremic spots

A

Oral thrush.

Plaques can be removed (even if difficult)

Residual area of inflammation normal after plaque removal

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11
Q

Small Flat Cherry-red Lesions in the colon

A

Angiodysplasia (vascular ecstasies or AV malformations)

Vascular anomalies composed of multiple aberrant blood located in GI tract. Frequent cause of occult bleeding.

Pathogenesis: chronic occlusion of submucosal veins- congestions- AV collaterals

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12
Q

Bleeding GI angiodysplasia associated with?

A

Small percent bleed. ^ bleeding associated with:
-ESRD
-Aortic stenosis
- Von Willebrand

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13
Q

Chronic Diarrhea MCC

A

IBS, IBD
Chronic Infection
Malabsorption Syndrome

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14
Q

Evaluation of Chronic Diarrhea

A

Complete Hx of Sxs

Routine Lab Tests
Electrolytes
Stool Analysis
Microscopic Stool examination (leukocytes, parasites, occult blood,pH, fat)
Stool Osmotic gap

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15
Q

Stool findings in celiacs

A

Increased stool osmotic gap
Micro cystic anemia, iron deficiency
Villous atrophy

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16
Q

Lactose intolerance stool findings

A

Diarrhea after lactose

Increased stool osmotic gap
Decreased stool pH
+ lactose hydrogen breath test

17
Q

Collagenous Colitis

A

Chronic watery diarrhea associated with fecal urgency and nocturnal diarrhea

Secretory diarrhea (decreased stool osmotic gap)

Thick subepithelial collagen band

18
Q

Further Management of celiacs (in addition initial tx: diet)

A

Monitor: iron, folate, calcium, and other vitamins (A, D, E, B12) monitored.

DXA scan to evaluate for bone loss (due to vitamin D deficiency)

pneumococcal vaccine due to associated hyposplenism.

19
Q

Eosinophilia Esophagitis
pathogenesis

A

Th2- mediated inflammatory response triggered by food antigen exposure

Conor bid atopic disease (asthma, eczema, food allergies)

20
Q

Eosinophilia esophagitis Sxs and Dx

A

Dysphasia
Heartburn & epigastric pain
Regurgitation
Food impaction

Dx: endoscopy and biopsy (eosinophils >15)

21
Q

Eosinophilic esophagitis Tx

A

Elimination diet (primary)
PPI
Topical glucocorticoids

22
Q

Risk factors infantile hypertrophic pyloric stenosis

A

Firstborn Male
Macrolide antibiotic exposure (< 2 weeks age)

23
Q

Infantile hypertrophic pyloric stenosis Tx

A

IV Fluids
Surgical Pyloromyotomy

24
Q

Infantile hypertrophic pyloric stenosis Sxs

A

Age 3-6 weeks

Projectile nonbilious emesis (immediate)
Hungry VOmiter
Visible peristalsis
Dehydration

Hypochloremic Hypokalemic metabolic alkalosis
Indirect hyperbilirubinemia

25
Q

Initial studies of suspected esophageal mural injury

A

Malloy Weiss: UpperGI endoscopy

Boerhaave: CXR (pneumothorax, pneumomediastinum, pleural effusion). CT water soluble contrast

26
Q

Mallory Weiss vs Boerhaave

A

bothe present with hematemisis.

Boerhaave: fever, chest pain, mediastinitis, pleural effusion, hemodynamic instability

27
Q

Complications of untreated celiac disease

A

At risk for Entropy they associated T cell Lymphoma.

Poor prognosis due to late presentation: 10 months

28
Q

Sxs of Enteropathy associciated T-cell Lymphoma

A

(Aggressive hematologist malignancy that affects the jejunum)

And Pain
B Symptoms
Bowel obstruction/ perforation
GI bleed

29
Q

pathogenesis of intussuscption

A

MCC: involves hyperplasia of intestinal lymphoid follicles (Peyer patches) in the ileocecal region following viral infection in children age 6 months to 3 years;

intussusception due to a pathologic lead point (eg, Meckel diverticulum)

30
Q

clinical findings in intussusception

A
  1. Sudden, intermittent abdominal pain & vomiting
  2. Sausage-shaped mass in right abdomen
  3. Currant jelly stools
  4. Lethargy or altered mental status
31
Q

next step in management of intussusception

A
  1. Classic presentation: Air or water-soluble both diagnostic and therapeutic.
  2. Atypical presentation (eg, lethargy alone): Ultrasonography is the diagnostic reveals a target sign. An enema can be performed once the diagnosis is confirmed.
32
Q

colon cancer screening with family

A

Colonoscopy at age 40 (or 10 years prior to age of diagnosis in FDR, whichever comes first)Repeat every 5 years (every 10 years if FDR diagnosed at age >60)

33
Q
A