Gastroenterology Flashcards

1
Q

Protein Intolerance (Milk Protein-Induced Enterocolitis)

A

o Majority of cases result of Milk Protein (can be from mom’s consumption of milk)
o Presents age2-8w
o Eczema
o Enteropathy
Diarrhea, Severe reflux/vomiting, colicky abdominal pain Chronic blood loss in stools can lead to anemia
Protein loss in stools causes FTT & Edema
o Enterocolitis Acute
Diarrhea, painless blood & mucus in stool
Protein loss in stools causes FTT & Edema o Tx
Breastfeeding mother remove protein (Milk & Soy)
Can continue to breast feed
Resolves by 1-2 y/o
Elemental (hydrolyzed) formula

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Hirschsprung Disease

A

o Typically rectosigmoid colon
o Also associated w/ Down Syndrome
o Normal meconium consistency
o S/Sx
Rectal examination reveals tight anal canal may lead to explosive expulsion “Squirt Sign”
Bilious or Feculent vomiting (newborns), abdominal distension, constipation (older children)
Failure to pass meconium Or delayed (>48 h)
o BariumSwallow
Dilated proximal bowel w/ narrow distal segment
o Dx
Screen
Anorectal manometry Diagnostic
Lack of ganglionic cells (NCC migration) on punch biopsy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Duodenal Atresia

A

o 1⁄4 Down Syndrome
o S/Sx
Bilious Vomiting w/in first 2 days of life Double Bubble Sign on XR
Air w/in distended stomach and proximal duodenum
o HxofPolyhydramnios
o Dx
Prenatal Ultrasound
o Associated with Down Syndrome
o Tx
Nasogastric decompression first IV Fluids & ABx
Surgery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Diarrhea/Vomiting and Dehydration

A

o Most commonly caused by Viral Gastroenteritis

o Hyponatremic, hypovolemic, hypoosmotic, low urine sodium, low serum osmolarity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Celiac

A

o Presents between 6m and 2y
o Gluten is in wheat, barley, rye, &oats
o S/Sx
Fatigue, weight loss
Diarrhea, vomiting, bloating
Abdominal pain & large foul smelling stools Dermatitis Herpetiformis
Erythematous Vesicles on extensors o Pruritic
o Associated w/ Vitiligo and T1DM
o Malabsorption
Osteoporosis/osteomalacia
Can lead to iron deficiency anemia
o Dx
Biopsy
Short villi, deep crypts, & vacuolated epithelium w/ lymphocytes
IgA endomysial Ab & Serum Tissue Transglutaminase Ab IgG in IgA deficient pt.
o Tx
Corticosteroids for severe diarrhea

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Short Bowel

A

o Malnutrition with carb & fat malabsorption w/ steatorrhea FTT
o Distalresection
↓ B12 & Bile Acid reabsorption
o Causes
Congenital
Gastroschisis, volvulus, or atresia that require resection Crohn’s, tumors, & radiation enteritis
o Complications
TPN cholestasis w/ resulting Gallstones Bacterial overgrowth
TPN induced Liver failure
o Tx
Early enteral feedings for remaining bowel & liver function Liver transplant

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

GER

A
o Normal physiologic state in which stomach contents move retrograde 
o “HappySpitters”
  w/out GERD Sx
  Benign emesis/spitting up
  Not related to over feeding
  Resolves by 6-12m
o Tx
  Reassurance
  Positioning therapy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Colic

A

o Crying in another wise healthy infant for >3h daily (usuallyevening), >3x per week, for a
duration of >3w
o Tx
Soothing techniques

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

GERD

A

o Infantspresentw/
Emesis/spitting up, Suboptimal calorie intake (feeding refusal), & if severe FTT Irritability
Sandifer Syndrome
Torticollis w/ arching of the back from painful esophagitis o Older Children presents w/ Typical GERD Sx
o Causes
Inappropriate Transient LES Relaxation (TLESR)
o Complications
Upper/lower Airway Disease
Induces bronchopulmonary constriction o Riskofaspiration
Chronic Laryngitis
William Martin MD MBA 2016 TTUHSC SOM OC USN
2.23.2015
o Hoarseness,wheezing,vocalcordnodules Barrett’s esophagus
FTT
Esophageal strictures o Dx
pH probe is gold standard
Bronchoscope w/ alveolar lavage when aspiration is strongly suspected o Tx
Conservative
Positioning & meal timing first (before pharmacotherapy)
Thickened feeds
H2 Blockers & PPI
Motility agents
Metoclopromide
o High side effects (1/3)
Drowsy, restlessness
↑ LES tone or Gastric Emptying Surgery
Nisses Funoplication
o Usually followed with gastrostomy tube to maintain
feedings/nutrition while stomach adjusts to ↓ volume

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Choledochal Cyst

A

o Congenital abnormality of biliary ducts
Dilation of intra or extra-hepatic biliary ducts or both o S/Sx
Infants
Jaundice, acholic stool (like biliary atresia)
Children
Abdominal pain, jaundice, recurrent pancreatitis, dark urine ↑Bilirubin
o Dx
US or MRI
Cystic Extrahepatic mass

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Hypertrophic Pyloric Stenosis

A

o Projectile Vomiting Nonbilious
Early in life, three to five weeks
Hypokalemic, hypochloremic, metabolic alkalosis (loss of H+)
High PCO2
Hypokalemia results from ↑ aldosterone in response to volume
depletion from vomiting
HCl, H2O, and NaCl lost in vomit
Will still seem hungry
o Risk Factors: w/ Trisomy 18, first born male, erythromycin, formula feeding
o Physical
Olive Mass (epigastric/RUQ)
Peristaltic Wave in abdomen after feedings
o Dx
US
Thickened and elongated pylorus Barium Swallow
May show string sign
o Small amount of barium getting past
o Tx
Correct electrolytes/dehydration (DON’T OPPERATE IF ELECTROLYTE
ABNORMALITIES)
Must correct, IV hydration + Potassium
Partial pylorectomy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Malrotation of the Gut & Midgut Volvulus

A

o Bilious vomiting

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Intussusceptions

A

o Peak5to9m
Before age 2 typically
o Ileocolic intussusceptions most common
Viral Gastroenteritis can also cause a lead point through inflammation of the Peyer’s patches
Hematomas from HSP & Mekel’s can also serve as lead points o S/Sx
Sudden crampy/colicky abd pain
Periods of Colic and then normal behavior (playing laughing) or
lethargic
Vomiting
Currant Jelly Stools (Bloody Mucus) from edema and sloughing of mucosa
Sausage shaped mass in RUQ o Dx
US
Target Sign
o Tx
Air/Contrast enema is gold standard
Avoid hydrostatic if prolonged, perforated, or peritonitis o Air is preferred
Coil Spring Sign
May reduce the intussusceptions (therapeutic)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

AbdominalRigidity

A

Peritoneal Process

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Restlessness

A

Colicky Pain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Constant Abdominal Pain

A

Suggests strangulation or torsion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Intestinal Obstruction PE

A

High pitched bowel sounds, abdominal distension, tenderness, & visible peristalsis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Peritonitis

A

↓/absent bowel sounds
Rigidity w/ guarding
Rebound Tenderness

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Appendicitis

A
Pain referred to T-10 (umbilicus)   PE
  Tenderness @ McBurng’s
  Guarding
  Rebound Tenderness
  ↑ WBC and neutrophils
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Acute Pancreatitis

A
Uncommon in children   Causes
  Trauma #1, idiopathic #2, infection
  S/Sx
  Pain @ periumbilicus & epigastric
o Radiatestoback
  Severe w/ blood along the fascial planes
o Gray Turner Sign
  Bluish discoloration of the flanks
o Cullen Sign
  Bluish discoloration of periumbilical
  Labs
  ↑ Amylase
  ↑ Lipase
  Abdominal US for Dx   CT for complications
  Pseudocyst formation   Tx
  ABx if Necrotizing
  Small Pseudocyst can resolve on own, but large ones may require
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Cyclic Vomiting Syndrome (CVS)

A
o Acute and frequent vomiting that resolves spontaneous w/ no Sx in between episodes 
o FHxofmigraines
o Thought to be linked to abdominal migraines
o Dx
  Criteria
  ≥3 episodes in 6-month
  Easily recognizable to family
  Lasts 1-10d
  Vomiting ≥4 times/hr @ peak
  No Sx in between episodes
  No underlying condition
o Tx
  Antiemetic (ondansetron [Zofran])   If FHx of migraines: Sumatriptan
22
Q

Cholecystitis

A
o Inflammation of the gallbladder
  Most commonly w/ stones
  Less commonly w/out (Acute Acalculous Cholecystitis) 
o Uncommon in children unless:
  CF, TPN, or Sickle Cell 
o RUQPainw/Guarding
o +Murphy’sSign
  Palpation of the RUQ upon inspiration, intense pain, inspiration ceases
o Imaging
  US
  Stone or thickened GB Wall
  Cholescintigraphy may be useful 
o Mild ↑ LFT & TB
o Tx
  ABx
  Cholecystectomy if peritonitis
23
Q

Constipation

A

o Risk factors: Dairy, toilet training, school entry o S/Sx
Abdominal pain, passage of pellet like stools, 48h)
Increase fiber, limit cow’s milk, laxative (polyethylene glycol, mineral oil)

24
Q

IBD

A
o Peaks 15 to 20 y/o & @ 50 y/o 
o Includes
  Crohn’s Disease
  Ulcerative Colitis 
o Tx
  Immunosuppressive Agents
  Induce long term remission
  Corticosteroids
  For acute exacerbation & induce remission
25
Ulcerative Colitis
``` o Limitedtocolon o Continuous & Limited to the Mucosa Mucosa is friable and bleeds o Typically bloody diarrhea w/mucosa At least 3-4w o Ranges in Severity Rectal Bleeding, diarrhea, abdominal pain, Hypoalbuminemia o P-ANCA o Complication Toxic Megacolon ↑ Risk for Colorectal Cancer o Tx Sulfasalazine Can be cured w/ total proctocolectomy, but reserved for intractable colitis Immunosuppressive Agents & Corticosteroids ```
26
Crohn's Disease
o Any segment (mainly terminal Ileum) Can have mouth ulcers o Skip lesions & segmental inflammation o Transmuralinflammation Fistulas, Crypt Abscesses, Strictures o Malabsorption Vit B12, Zinc, Folate, Fe2+ o Perianal disease (verycommon) often precedes intestinal disease Skin Tags, abscesses, fistulas o ExtraintestinalManifestations Much more common than in UC FUO, arthritis, mouth ulcers, skin manifestations (erythema nodosum), weight loss, malaise, and growth retardation o Anti-SaccharomycescerevisiaeAb o Granulomas(30%) o Imaging String Size Thickened bowel folds w/ narrowing of the tract o Tx Metronidazole When fistulas presents Esp. w/ inflammation Immunosuppresive Agents & Corticosteroids Azathioprine, cyclosporine, tacrolimus, TNF-α
27
GI Bleed
``` o Hematemesis Coffee ground appearance o Hematochezia Bright red, lower GI or significant rapid upper GI o Melena Dark tarry, upper GI (proximal to Ligament of Treitz) o Occult bleeding from GI Guaiac + False + o Ingested iron False - o Large amounts of ingested Vit. C ```
28
Upper GI Bleed
``` o Swallowed maternal blood o Endoscopy if active bleeding w/hemodynamic changes o Tx Initial: Fluid Bolus w/ IV access Octreotide for varices PPIs Arteriographic embolization for serious bleeding Vascular malformations ```
29
Necrotizing Enterocolitis (NEC)
Consider in any newborn w/ rectal bleeding, feeding intolerance, & abdominal distension More common in prematures & Low birth weight Immaturity of the stomach plus exposure to bacteria from enteral feeds leads to bowel inflammation and damage Caused by local ischemia, dilation, and infarction of loops of bowel S/Sx Abdominal distension, Hematochezia (or occult blood), pneumatosis intestinalis (air in the bowel wall, double line/train track appearance) Blood in NG tube Complications Intramural air spreading to portal vein (venous portal gas) Later on intestinal perforation o Pneumoperitoneum Breast feeding reduces the risk of NEC Tx Mild o Decompression, electrolyte repletion, IV ABx, serial abdominal exams checking for perforation Severe (perforation) o Severe if perforation (free air on lateral decubitus or under diaphragm), fixed dilated bowel on serial X-rays, abdominal wall cellulitis o Surgical resection and reanastomosis (exploratory laparotomy) Following surgery, parenteral feeds for 14d Allows for bowel rest
30
Juvenile Polyps
``` Lower GI bleeding: #1 cause beyond infancy (>5y?) Bleeding is painless, intermittent, & often streaky Tx Colonoscopy w/ polypectomy ```
31
Allergic Colitis
Sensitization to milk protein
32
Infectious Enterocolitis
Salmonella, Shigella, Yersinia, & E. Coli
33
Meckel's Diverticulum
Outpouching terminal ileum | Infants 2% (typically
34
HUS
Intestinal ulceration & infarction of the bowel cause bleeding
35
Hepatocellular Enzymes
``` o AST Sensitive, but not specific o ALT Specific for liver disease o LDH Nonspecific for liver disease, but may serve as a marker for liver necrosis ```
36
Biliary Enzymes
o Alkaline Phosphate ↑ in Biliary Disease Can also be ↑ in Rapid Growth, Renal/GI disease, & trauma o Gamma Glutanyl Transpeptidase &5NT ↑ Biliary disease 5NT more specific than GGTP for biliary tract disease
37
Infant Jaundice
o ↑TB Clinically evident TB > 3 o Kernicterus Risk w/ indirect hyperbilirubinemias ≥20 Risk factors Sulfisoxazole and other drugs that bind albumin and ↑ dissociation of bilirubin Metabolic acidosis, ↑ bilirubin dissociation Hypoalbuminemia Sepsis o Interrupts BBB Phenobarbital induces glucuronyl transferase
38
Normal Physiologic Jaundice
First 2-4d of life (peak) No higher than 12 mg/dL Disappears by 1w Rate of rise
39
Breastfeeding Jaundice
``` Inadequate calories & dehydration Breast feeding failure: inadequate feedings, poor latching ↑ enterohepatic circulation o Indirect Hyperbilirubinemia Signs of dehydration o Decreased wet diapers o May not regain birth weight o Brick red urate crystals in diapers Typically second to fourth day (first week) Tx Rehydrate w/ fluids or formula Lactation consult o Should be breastfeeding ever 2-3h for 10-20mins each breast Threshold for phototherapy o 4dold >20 Threshold for transfusion therapy o 4dold >25 ```
40
Breastmilk Jaundice
Enzyme in milk is inhibitor of glucuronyl transferase ↑ indirect bilirubin Gaining weight, no signs of FTT Typically during second week (>7d) Tx If Pathological (~17-20) DC breast feeding for 1 to 2d, formula then o Resume breast feeding after precipitous drop in TB w/out fear of rise to toxic levels Reassurance if levels are not too high
41
Cholestatic Jaundice
Retention of bile in liver | Direct Bilirubin > 2
42
Cholestasis
> 50% caused by neonatal hepatitis or Biliary Atresia | If suspect cholestasis, HIDA Scan
43
Inspissated Bile Syndrome
Associated w/ Hemolysis or very large hematoma | Starts w/ ↑ Indirect, but switches to ↑ direct as the liver ramps up
44
UDP-Glucuronyl Transferase Deficiencies
``` Gilbert's Syndrome 50% Enzyme Mild Jaundice w/ stress or poor nutrition Crigler Najjar Indirect Hyperbilirubinemia TypeI o 100%Enzymeabsent o AR o Kernicterus caused by ↑ TB Type II o 90%EnzymeDeficient o AD o Bilirubin lvls are variable w/ ↓ chance of Kernicterus ```
45
Biliary Atresia
o Progressive fibrosclerotic changes of extrahepatic bile ducts o Presents w/in first 2m of life o S/Sx Jaundice, dark urine, acholic (pale) stools Moderate ↑ TB Direct Hyperbilirubinemia Rapid progression w/ Bile duct obliteration & cirrhosis by 4m Hepatomegaly, Ascites, Coagulopathy, Edema o Some have associated Polysplenia Syndrome Bilobed lings, abdominal Heterotaxy, & situs invertus o Dx First perform US Lack of Gallbladder and Triangle Sign Will also catch other Gall Bladder DO Hepatobiliary Scintigraphy Failure of tracer excretion from liver Intraoperative cholangiogram w/ Laparotomy to examine biliary tree (gold standard) o Tx Kasai Portoenterostomy Establishes bile flow by attaching intestinal loop to porta hepatis Success is highest if
46
Heb B Tx
Tx | All newborns of mothers w/ active Hep B (HbsAG, HBeAG + esp.) receive HBIG (Hep B immune globulin) & Vaccine
47
Autoimmune Hepatitis
o Destructive&Progressive o ↑ serum transaminases, hypergammaglobulinemia, auto-Ab o Types Type I ``` Type II o Females before o S/Sx 50% w/ Antinuclear Ab (ANA) or Anti-Smooth muscle Ab More common than Type II Anti-Liver Kidney Microsomes? puberty Acute Hepatitis Mimics viral hepatitis 50% Chronic liver disease Mild to Moderate Jaundice o Tx Corticosteroids Immunosuppressive Agents Azathioprine 6-MP ```
48
Lead Poisoning Tx
Remove from environment.
49
Esophageal Atresia
o Vomiting, choking, coughs w/ first feeds o Frothing at mouth o May have respiratory distress, abdominal distension depending on fistula presence/location o Associated w/ VACTER Constellation Vertebral anomalies, anal atresia, cardiovascular anomalies, transesophageal fistula, renal/radial anomalies Usually accompanied by tracheoesophageal fistula leading to abundance of gas in GI tract o Immediate coiling of nasogastric tube confirms
50
Mallory-Weiss Tear
o Lower esophageal tear from forceful retching w/ or w/out vomiting Hematemesis Painless bleeding
51
Beckwith-Wiedmann Syndrome
``` o Overgrowth Syndrome w/ predisposition to neoplasms Neoplasms Wilm’s Tumor & Hepatoblastoma o Screening w/ Abdominal US and AFP Large-sized patients Hemihyperplasia Macrosomia Macroglossia Liver/Kidney enlargement Hyperinsulinism Hypoglycemia at birth Midline abdominal defects Omphalocele, umbilical hernia ```