GI Flashcards

0
Q

Diaphragmatic Hernia

Def’n, Mech, Pres (Age Group)?

A

Ab structures enter thorax.

MECH = Defective devel of pleuroperitoneal memb.

PRES: Infants

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1
Q

Sliding Hiatal Hernia

Mech (3 steps), Pres (CLUE)?

A

MECH:
LES slides SUP -> GE junction displaced ->
Diaphragm can no longer reinforce it.

PRES:
- “Hourglass stomach”

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2
Q

Rolling / Paraesophageal Hernia

Def’n?

A

FUNDUS protrudes into thorax. GE junction normal.

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3
Q

Indirect Inguinal Hernia

Def’n, Embryo, Mech, Anat, Pres (Epi)?

A

Projects through INGUINAL RING.

Follows path of descent of testes.
Covered by all 3 layers of spermatic fascia.

MECH = Failure of PROCESSUS VAGINALIS to close.

** LATERAL to inf epigastric art. **

PRES = MC in Males

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4
Q

Direct Inguinal Hernia

Def’n, Embryo (layer of spermatic fascia covered by), Anat, Pres (Epi)?

A

Projects through AB WALL.

Covered by EXTERNAL layer of spermatic fascia only!

** MEDIAL to inf epigastric art. **
Passes thr Hesselbach’s Triangle -> SUP Inguinal Ring only!

PRES = MC in older men

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5
Q

Femoral Hernia

Def’n, Anat, Pres (Epi)?

A

Part of S.I protrudes through femoral ring.

Protrudes below inguinal ligament.

PRES = MC in Women (wider bony pelvis)

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6
Q

SMA Sx

Def’n?

A

Transverse portion of Duodenum entrapped b/w Aorta + SMA -> Intestinal Obstruction.

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7
Q

Internal Hemorrhoids

Anat, Innervation, Pres (CLUE), Assoc?

A

ABOVE pectinate line.

Visceral innervation.

PRES = NOT painful.

ASSOC:
- Portal Htn

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8
Q

External Hemorrhoids

Anat, Innervation, Pres?

A

BELOW pectinate line.

Somatic innervation (inf rectal branch of pudendal nerve).

PRES = Painful.

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9
Q

Anal Fissure

Def’n, Location, Pres (2)?

A

Tear in anal mucosa.

BELOW pectinate line.

PRES:

  • Painful defecation
  • Blood on toilet paper
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10
Q

Esophageal Webs

Def’n, MC Location?

A

Thin protrusions of esophageal mucosa.

MC in UPPER Esophagus.

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11
Q

Esophageal Varices

Def’n + Location, Cause, Pres, Comp?

A

Dilated submucosal veins in LOWER 1/3 of Esophagus.

CAUSES:
- Portal Htn

PRES = PAINLESS / Asymptomatic bleeding

COMP = ** Rupture **

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12
Q

Esophageal Strictures

Assoc (2)?

A

ASSOC:

  • Lye ingestion
  • Acid reflux
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13
Q

Esophagitis

Causes (4: 3 Micro + 1)?

A

CAUSES:

  • HSV-1 (“punched-out” ulcers) in immunocompromised p/ts
  • CMV (“linear” ulcers)
  • Candida (“white pseudomemb”)
  • Chemical ingestion
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14
Q

Eosinophilic Esophagitis

Def’n (incl Epi), Cause, Pres (Triad + 1)?

A

Infiltration of eosinophils into esophaguses of ATOPIC P/TS.

CAUSE = Exposure to food allergens.

PRES:

  • Triad:
    1. Strictures
    2. Dysphagia
    3. Heartburn
    • Unresponsive to GERD therapy *
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15
Q

Dysphagia

  • To solids only -> ?
    - Causes?
  • To solids + liquids -> ? (Progressive = solids first then liquids)
    - Causes (3)?
A
- Obstruction 
           CAUSES:         
            - Esophageal Web (eg Plummer-Vinson Sx) 
- Progressive Dysphagia
            CAUSES:
            - Achalasia
            - Esophageal SCC 
            - Peristalsis problem
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16
Q

Achalasia #1

Def’n, Causes, Assoc (2)?

A

Achalasia = absence of relaxation.

MECH:
↑LES tone due to loss of Myenteric (Auerbach’s) plexus.
-> HIGH LES opening pressure + UNCOORDINATED peristalsis.

CAUSES:
- Nitric Oxide secretion loss

ASSOC:

  • Chagas Dz
  • Scleroderma / CREST Sx (esophageal dysmotility due to LOW pressure proximal to LES)
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17
Q

Achalasia #2

Pres, Appearance on Ba Swallow (CLUE)?

A

PRES:
- Progressive dysphagia to solids + liquids

BA SWALLOW:
- “Bird’s beak” (dilated esoph with area of distal stenosis)

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18
Q

GERD

Def’n, Pres (CLUE + 2), Comp?

A

↓in LES tone.

PRES:

  • “Heartburn + Regurg upon LYING DOWN”
  • Nocturnal dyspnea + cough
  • Adult-onset Asthma

COMP:
- Barrett’s

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19
Q

Mallory-Weiss Sx

Def’n, Pres (Epi CLUE + Pres CLUE), Comp?

A

Gastroesophageal lacerations due to frequent + severe vomiting.

PRES: Alcoholic + Bulimic patients
- “PAINFUL hematemesis”

COMP:
- Berhaave Sx

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20
Q

Boerhave Sx (** “Been-Heaving Sx” **)

Def’n?

A

Transmural esophageal RUPTURE -> Air in Mediastinum ->

Subcutaneous Emphysema.

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21
Q

Plummer-Vinson Sx

Pres (3), Comp (progression to)?

A

PRES: ** “Plumbers DIG” **

  • Dysphagia ( / Esoph Webs)
  • Iron Deficiency Anemia
  • Glossitis (Atrophic)

COMP:
- Esophageal SCC

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22
Q

Barrett’s Esophagus

Mech + Location, Cause, Comp?

A

Glandular Metaplasia- replacement of normal esoph epithelium with INTESTINAL (COLUMNAR) epithelium + Goblet cells.

DISTAL Esophagus.

CAUSE = Chronic GERD

COMP:
- 30-40x↑risk of Esophageal SCC

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23
Q

Esophageal Cancer

Pres (4), Prog?

A

PRES:

  • Progressive dysphagia
  • Weight loss
  • Pain
  • Hematemesis

PROG = Poor. (Worse with later pres)

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24
Q

Esophageal SCC

Location, RF (3), Causes / Assoc (7), Pres (2)?

A

UPPER 2/3 of Esophagus.

RF:

  • Very hot tea
  • Cigarettes
  • Alcohol

CAUSES / ASSOC:

  • Diverticula
  • Achalasia
  • Esoph strictures
  • Mallory-Weiss Sx
  • Berhaave Sx
  • Plummer-Vinson Sx
  • ** Barrett’s **

PRES:

  • Hoarse voice
  • Cough
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25
Q

Esophageal Adenocarcinoma

Location, RF (2)?

A

LOWER 1/3 of Esophagus.

RF:

  • Esophagitis
  • Barrett’s
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26
Q

Acute Gastric Ulcers

2 Types: Mech of Production, Assoc?

A

CURLING ULCER:
Greatly↓PLASMA VOLUME -> SLOUGHING of gastric mucosa.
ASSOC = SEVERE BURNS

CUSHING ULCER: ↑INTRACRANIAL P -> ↑Vagal gastric secretion.
ASSOC = CNS injury

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27
Q

Acute Gastritis

RF (3 ‘substance consumers’ + 2 general states + 2 specific traumas)?

A

RF:

  • Alcoholics
  • P/ts taking daily NSAIDs (↓PGE1 -> ↓gastric mucosa protection)
  • P/ts on Chemotherapy
  • Stress
  • Shock / Trauma
  • Burns
  • Brain injury
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28
Q

Chronic Atrophic / Autoimmune Gastritis

Mech, Comp (2)?

A

MECH = Autoimmune destruction of Parietal cells

COMP:

  • Pernicious Anemia
  • Gastric Carcinoma
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29
Q

Type A (fundus / body) Chronic Gastritis = Autoimmune Gastritis

Ab (2), Path, Pres, Labs (2), Prog?

A

Autoantibodies against Parietal cells and/or Intrinsic Factor.

PATH: T cell-mediated = Type 4 H-S.

PRES:
- Pernicious Anemia

LABS:

  • Gastrin↑
  • Cl↓

PROG:
- ↑risk for Gastric Carcinoma

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30
Q

Type B (antrum) Gastritis = H pylori Gastritis

Mech, Pres,
RX (incl 2 signs of eradication + 2 goals of therapy), Comp (3)?

A

MECH = Weakening of mucosal defenses due to:

  • H pylori Proteases + Ureases
  • Infl

PRES:
- Epigastric ab pain

RX = Triple Therapy: PPI + Amoxicillin + Clarithromycin
(Metronidazole if allergic to penicillin)
* Eradication when Urea Breath Test + Stool Antigen negative *
-> Elimination of gastritis / ulcer
-> Reversal of intestinal metaplasia

COMP:

  • Ulceration / Peptic Ulcer Dz
  • Gastric Adenocarcinoma
  • MALT Lymphoma
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31
Q

Peptic Ulcer Disease

Def’n, 2 Types, Mech, RX, Comp (3)?

A

Solitary mucosal ulcer.

  • Gastric ulcer
    • Duodenal ulc

MECH = ↓mucosal protection against gastric acid

RX = (same as for H Pylori Gastritis if caused by H Pylori)

COMP:

  • Rupture
  • Acute Pancreatitis (rupture of POST ulcer)
  • 1ry Hyperparathyroidism
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32
Q

Menetrier’s Dz

Pres (General Triad + CLUE)?

A

Precancerous

PRES:

  • “Rugae of stomach so hypertrophied that they look like brain gyri”
  • Triad:
    1. ↑mucous cells
    2. Parietal cell atrophy
    3. Protein loss
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33
Q

Gastrinoma

Def’n, Pres?

A

Gastrin-secreting tumor ->↑acid secretion -> Ulcers.

PRES = Gastric Ulcers

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34
Q

Gastric Adenocarcinoma

Def’n, Path (2, incl 3 mets), Assoc (3), Pres (3)?

A

Malignant proliferation of gastric surface epithelial cells.

PATH:

  • Early aggressive local spread
  • Mets:
    - Virchow’s node
    - Sister Mary Joseph’s nodule
    - Krukenberg tumor

ASSOC:

  • Type A blood
  • Achlorhydria
  • Chronic Gastritis

PRES: * Late *

  • Ab pain
  • Early satiety + Weight loss
  • Anemia
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35
Q

Intestinal Gastric Adenocarcinoma

Location, Appearance, Assoc (2), Pres (CLUE)?

A

MC on Lesser Curvature of Stomach.

Resembles gastric ulcer (large + irregular with raised margins).

ASSOC:

  • Smoke (tobacco smoking + smoked foods)
  • H pylori infection

PRES:
- Sister Mary Joseph’s nodule (subcutaneous periumbilical mets)

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36
Q

Diffuse Gastric Adenocarcinoma

Pres (2 CLUES)?

A

PRES:

  • Signet Ring cells that DIFFUSELY INFILTRATE gastric wall
  • “Linitis Plastica” (thick + leathery stomach wall)
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37
Q

Krukenberg’s Tumor

Def’n, Micro Findings (2: CLUE + General)?

A

Diffuse Stomach Cancer -> Bilateral Mets to Ovaries.

FINDINGS:

  • “Signet Ring” cells
  • Abundant mucus
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38
Q

S.I Infarction

2 Types, Mech (Transmural), Pres?

A
  • Transmural Infarction
  • Mucosal Infarction

MECH (Transmural Infarction):
Thrombosis / embolism of Mesenteric artery or vein.

PRES = Severe Htn

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39
Q

Malabsorption Sx

Pres (5), Dx?

A

PRES:

  • Diarrhea: bloody + steatorrhea
  • Ab distension + pain
  • ↓bowel sounds
  • Weight loss (Adult) / Failure to thrive (Child)
  • Weakness

DX = Steatorrhea!

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40
Q

Tropical Sprue

Location?

A

Can affect ENTIRE S.I.

** Difference from Celiac Sprue **

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41
Q

Whipple Disease (Tropheryma whipplei)

Locations (4),
Pres (Epi + 3 Categories: “Foamy whipped cream in a CAN”),
Micro Finding?

A
  • Nodes: Intestinal or Mesenteric
  • CNS
  • Heart valves
  • Synovia

PRES: Older men

  • Cardiac symptoms
  • Adenopathy + Arthralgias
  • Neuro symptoms:
    - Fever
    - Weight loss

FINDING:
- PAS-positive foamy macrophages

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42
Q

Celiac Sprue

Def’n, Locations (2), Ab, HLAs (2),
Pres (Epi + 1 Assoc), Micro Findings (CLUE + 2),
RX?

A

Autoimmune-mediated damage to S.I VILLI due to gluten exposure.

Distal Duodenum and/or Proximal Jejunum

Anti-Gliadin / Anti-Transglutaminase / Anti-Endomysial Antibodies

HLA-DQ2 + HLA-DQ8
THINK: “Shaina was diagnosed at 28.”

PRES: MC in ppl of Northern European descent
- Dermatitis Herpetiformis (due to IgA deposition at tips of dermal papillae)

FINDINGS:

  • “Blunting / flattening” of villi
  • Hyperplasia of crypts
  • Lymphocytes in lamina propria

RX = Gluten-free diet

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43
Q

Lactose Intolerance

Def’n, Mech (2 steps), Pres, Dx?

A

Absence of brush border Lactase.

MECH:
Undigested lactose = osmotically active ->
UNABS lactose + water in GI tract lumen.

PRES = Osmotic Diarrhea

DX: Lactose Tolerance Test

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44
Q

Abeta-Lipoproteinemia

Def’n, Inher, Mech (3 steps), Pres (Epi + 3)?

A

Deficiency of apolipoproteins B-48 + B-100.

AR.

MECH:
Deficicency of apolipoproteins B-48 + B-100 ->
Inability to generate chylomicrons (B-48) + LDL/VLDL (B-100) ->
Fat accumulation in enterocytes = Malabsorption.

PRES: Early childhood

  • Failure to thrive
  • Neuro manifestations: Ataxia + Night Blindness
  • Acanthosis
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45
Q

Zollinger-Ellison Sx

Def’n / 2 Locations, Pres (2)?

A

Gastrinoma of Duodenum or Pancreas.

PRES:

  • High Gastrin
  • Duodenal ulcerations
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46
Q

“Red currant jelly stools”

Seen In (2)?

A

SEEN IN:

  • Intussusception (Infants)
  • Acute Mesenteric Ischemia (Adults)
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47
Q

Intussusception

Def’n + Location, Mech, Causes, Pres (Epi + CLUE + 1)?

A

Intussusception / “telescoping” of Terminal Ileum into Cecum.
(Pulled forward by peristalsis)
** THINK: In word ‘intussusception’, i comes before c.
= Ileum into Cecum. **

MECH = Obstruction + Infarction.

CAUSES:
- Meckel’s Diverticulum

PRES: MC in children

  • “Currant jelly” / bloody stools (due to compromised bl supply)
  • Colicky ab pain
  • ** Ab emergency in early childhood ***
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48
Q

Volvulus

Def’n, MC Locations (2, incl Epi of each), Mech, Causes?

A

Twisting of portion of colon around its mesentery.
(In parts of colon where there is redundant mesentery)

  • Cecum (MC in young adults)
  • Sigmoid Colon (MC in elderly)

MECH = Obstruction + Infarction

CAUSES:
- Meckel’s Diverticulum

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49
Q

Meckel’s Diverticulum

Etiology, Histo (2 types of epithelia), Chars (** “5 2s” **),
Pres (2 Epi + 5), DX?

A

ET = Persistence of vitelline duct

2 types of epithelia:

  • Gastric mucosa (ectopic acid-secreting)
  • Pancreatic

CHARS:

  • 2 inches long
  • 2 feet from ileocecal valve
  • 2 types of epithelia
  • 2 yrs of life
  • 2% of pop

PRES: First 2 yrs of life. 2 % of pop.

  • Obstruction near Terminal Ileum
  • RLQ pain
  • Melena
  • Intussusception
  • Volvulus

DX: Pertechnetate Study

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50
Q

Diverticulosis

Etiology, Causes (2), Pres (CLUE), Comp (2)?

A
Many diverticula -> diverticulosis. 
Very common (~50%) of people > 60 yrs.

CAUSES:

  • FOCAL WEAKNESS in colon wall
  • ↑intraluminal pressure

PRES:
- “PAINLESS rectal bleeding”
(Often asymptomatic or vaguely uncomfortable)

COMP:

  • Diverticulitis
  • Fistulas
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51
Q

Diverticulitis

Def’n, Pres (4), Comp (1 + CLUE), RX?

A

Infl of diverticula due to OBSTRUCTING FECAL MATERIAL.

PRES: ** “L-sided Appendicitis” **

  • “Bright red” rectal bleeding
  • LLQ pain
  • Fever
  • Leukocytosis

COMP:

  • Perforation -> Peritonitis
    - > Abscess formation
    - > Stenosis
  • “Colovescial fistula” (fistula with bladder) -> “air or stool in urine”

RX: Antibiotics

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52
Q

Inflammatory Bowel Disease (IBD)

Def’n, 2 Subtypes,
Pres (3 Epi + 1), EXTRAintestinal Manifestations (5),
Comp (2), RX (1 in common)?

A

Chronic and relapsing infl of bowel.

  • Crohn’s Dz
  • Ulcerative Colitis.

PRES: Young women. MC in West.
MC among Caucasians + Eastern-European Jews.
- Recurrent bouts of ab pain + BLOODY DIARRHEA

  • Apthous Ulcers (cankers)
  • Erythema Nodosum
  • Pyoderma Gangrenosum
  • Uveitis
  • Ankylosing Spondylitis

COMP:

  • Malabsorption / Malnutrition
  • CRC

RX: Infliximab

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53
Q

Crohn Disease

Etiology, Location, Mediation,
Gross Findings (3 CLUES + 2), Micro Finding,
Pres (2 Intestinal + 3 Extra-Intestinal),
Appearance of bowel on Ba Swallow (CLUE),
Comp (2), RX (3)?

A

Disordered response to intestinal bacteria.

ANY portion of GI tract, however MC in Terminal Ileum + Colon =
“Skip lesions” (alternating areas of normal colon + transmural infl).
Rectal SPARING.

Th1-mediated.

FINDINGS:

  • “Cobblestone mucosa”
  • “Creeping fat”
  • Bowel wall thickening -> “String Sign” (due to strictures)
  • TRANSMURAL infl
  • Linear ulcers, fissures + fistulas
  • Noncaseating granulomas + lymphoid aggregates

PRES:

  • Diarrhea (bloody or non-bloody)
  • RLQ pain (ileum)
  • Vit B12 def -> Macrocytic Megaloblastic Anemia
  • Kidney stones
  • Migratory polyarthritis ** THINK: Skipping **

BA SWALLOW: “String Sign” (strictures = narrowing of lumen)

COMP:

  • Stones: Ca Oxalate kidney stones + Gallstones
  • Perianal dz

RX:

  • Corticosteroids
  • Immunomodulators: Azathioprine + Methotrexate
  • Infliximab
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54
Q

Ulcerative Colitis

Etiology, Mech, Location, Mediation,
Gross Findings (CLUE + 2), Micro Finding,
Pres (Intestinal + Extra-Intestinal),
Appearance of bowel on Ba Swallow (CLUE),
Comp, RX (4, incl 1 procedure)?

A

Autoimmune.

MECH = Loss of haustra

Colon = CONTINUOUS lesions.
Rectal INVOLVEMENT.

Th2-mediated. ** THINK: 2 words **

FINDINGS:

  • “Friable mucosal pseudopolyps”
  • MUCOSAL + SUBMUCOSAL infl only
  • Freely hanging mesentery
  • Crypt abscesses + ulcers

PRES:
- BLOODY diarrhea

  • Primary Sclerosing Cholangitis

BA SWALLOW: “Lead pipe” appearance of colon

COMP:
- Toxic Megacolon

RX:

  • Sulfasalazine
  • 6-MP
  • Infliximab
  • Colectomy
55
Q

Ischemic Collitis

MC Location, Causes (MCC), Pres (Epi + 2)?

A

MC at Splenic Flexure (watershed area of SMA).

MCC = Atherosclerosis of SMA

PRES: Elderly

  • Pain after eating -> Weight loss
  • (In case of Infarction) -> Pain + Bloody Diarrhea
56
Q

Necrotizing Enterocolitis

Def’n, Pres (Epi)?

A

Necrosis of colon MUCOSA. Possible perforation.

PRES: Neonates (MC in preemies due to↓immunity)

57
Q

Colonic Polyps

Def’n, MC Location,
Subtypes (4, last 3 = benign / hamartomatous),
Pres (3 general ‘polyp symptoms’),
Screening (2)?

A

90% non-neoplastic
Raised protrusions of colonic mucosa protruding into gut lumen ->”sawtooth” appearance.

MC in LEFT Colon (rectosigmoid).

Can be tubular or villous.

  • Adenomatouuus
  • Hyperplastic
  • Juvenile / Juvenile Polyposis Sx
  • Peutz-Jeghers Sx

PRES: Often assymptomatic

  • Lower GI bleed (due to polyps bleeding)
  • SECRETORY diarrhea
  • Partial obstruction

SCREENING:

  • Colonoscopy -> Polyp removal + examination
  • Fecal Occult Bl test
58
Q

Gardner Sx

Def’n, Pres (CLUE + 2), Comp?

A

FAP+ Fibromatosis (retroperitoneal) + Osteomas (MC in Skull).

PRES:

  • “↑# of teeth => impacted teeth”
  • Multiple colonic polyps
  • Osteomas in skull

COMP:
- Congenital hypertrophy of retina (due to osteomas in skull)

59
Q

Adenomatous Polyps

Cause, Malignant RF (3)?

A
*Precancerous = precursor to CRC*
CAUSE = glandular neoplastic prolif.

MALIGNANT RF:

  • ** - Villous histology of polyp (↑=↑risk of malignancy) ***
  • ↑size
  • ↑epithelial dysplasia
60
Q

Familial Adenomatous Polyposis (FAP)

Locations (2), Inher, Genetics, Pres, RX?

A

100% progress to CRC
Colon + Rectum.

AD.

AD mutation of APC gene (chr 5q). “Two-Hit Hypothesis”.

PRES = Thousands of polyps

RX = Prophylactic removal of colon + rectum

61
Q

Turcot Sx

Def’n?
** THINK: Turban **

A

FAP+ Malignant CNS tumor.

62
Q

Peutz-Jeghers Sx

Def’n, MC Location, Inher, Pres (CLUE)?

A
*Malignant risk*
MULTIPLE Hamartomas (benign) throughout GI tract.

MC Location = Small Intestine.

AD.

PRES:
- “Hyperpigmented / freckle-like spots on lips, mouth, hands + genitalia”

63
Q

Juvenile Polyps / Juvenile Polyposis Sx

Def’n (both), MC Location, MC Pres?

A

Juvenile Polyps = sporadic lesions in children

64
Q

HNPCC / Lynch Sx

MC Side, Inher, Genetics, Pres (general)?

A

80% progress to CRC
MC side = RIGHT.

AD.

AD mutation of DNA Mismatch-Repair genes.

MC Side = Right

PRES = Arises “de novo” at relatively early age.

65
Q

Colorectal Cancer

Def’n, MC Side,
Molecular Path (2 pathways + what each lead to),
RF (5), Pres (2 Epi), Appearance on Ba Swallow (CLUE),
Screening, DX (3), Comp (2)?

A

Carcinoma arising from colonic or rectal mucosa.

MC Side = LEFT.

  • Microsatellite Instability Pathway (DNA Mismatch-Repair gene mut)-> Sporadic Cancer + HNPCC Sx
  • Chr Instability Pathway (APC + b-Catenin mut. 85%) -> Sporadic Cancer
  • ** Order of gene events: “A, K, 53” ***

RF:

  • Tobacco use
  • Lynch Sx / Juvenile Polyposis Sx / Peutz-Jeghers Sx
  • IBD
  • Large villous adenoma
  • Strep bovis bacteremia

PRES: > 50 yrs. 25% have family history.

BA SWALLOW: “Apple core” lesion

SCREENING:
- Begins at 50 yrs with Fecal Occult Blood Testing + Endoscopy

DX:

  • “Apple core” lesion on XR
  • CEA tumor marker (monitoring of treatment response + recurrence)
  • Iron-Deficiency Anemia in older adult = CRC until proven otherwise!

COMP: (Strep bovis colonization of gut)

  • Subacute Endocarditis
  • Bacteremia
66
Q

Right / Ascending / Proximal Colon CRC

Chars (2), Pres (3)?

A

CHARS:

  • Exophytic mass
  • Grows as a “raised lesion”

PRES:

  • Fecal Occult bleeding -> Iron-Deficiency Anemia
  • Vague pain
  • Weight loss
67
Q

Left / Descending / Distal Colon CRC

Chars (2), Pres (2), Appearance on XR (CLUE)?

A

CHARS:

  • Infiltrating mass
  • Partial obstruction

PRES:

  • Hematochezia +↓stool caliber
  • LLQ colicky pain

XR: “Napkin ring” lesion

68
Q

Acute Appendicitis

Mech (General + Children + Adults),
Pres (2 MC signs + 2 other signs + CLUE + Triad),
DDX (2), Comp (2)?

A

MECH: Obstruction of appendix

  • Viral infection -> lymphoid hyperplasia (Children)
  • Fecalith (Adults)

PRES:

    • McBurney Sign + Rovsing Sign
  • Obturator + Psoas signs
  • “Initial diffuse periumbilical pain” -> “Pain localizes to McBurney pt”
  • Fever + Nausea + Anorexia

DDX:

  • Ectopic Pregnancy
  • Diverticulitis (Elderly)

COMP:

  • Rupture (-> Peritonitis)
  • Abscess
69
Q

Peritonitis

Pres (CLUE)?

A

PRES:

- “Rebound tenderness” upon ab palpation

70
Q

McBurney Sign

Def’n, Seen In?

A

Severe RLQ pain + REBOUND TENDERNESS.

SEEN IN:
- Acute Appendicitis

71
Q

Rovsing Sign

Def’n, Seen In?

A

Severe RLQ pain + PALPATION OF LLQ.

SEEN IN:
- Acute Appendicitis

72
Q

Liver Disease

Enzyme↑(2)?

A
  • AST

- LD1 + LD5

73
Q

Angiodysplasia

MC Location, Mech (3 steps), Pres (Epi + 1), DX?

A

R Colon: Terminal Ileum + Ascending Colon + Cecum
(due to highest wall tension)

MECH:
Malformation of mucosal + submucosal CAPILLARY BEDS ->
Tortuous dilation -> Bleeding.

PRES: MC in Elderly
- Hematochezia (in case of rupture)

DX:
- Angiography

74
Q

Fatty Liver Disease

Etiologies (2), Micro Finding (CLUE)?

A

ET: Alcoholic or Metabolic Sx

FINDINGS:
- Fatty infiltration of hepatocytes -> hepatocyte “ballooning”+ eventual necrosis

74
Q

Liver Damage

Enzyme↑(2)?

A
  • ALT

- LD4 + LD5

74
Q

Hirchsprung’s Dz

Def’n + Locations (2), Mech (3 steps), Assoc,
Pres (4), DX (3), Comp, RX?

A

Congenital failure of GANGLION CELLS to descend into 2 plexuses:
Auerbach’s / Myenteric + Meissner’s / Submucosal plexus.

MECH:
Defective relaxation / peristalsis of SIGMOID COLON + RECTUM ->
Dilated portion of colon proximal to aganglionic segment ->
‘Transition Zone’.

ASSOC:
- Down’s Sx

PRES: ** Based on OBSTRUCTION **. Very early in life.

  • Failure to pass meconium
  • Ab distension
  • Constipation
  • Bilicus emesis

DX:

    • Failure to pass meconium
  • DRE: Empty rectal ampulla / vault
  • Rectal Suction Biopsy: Lack of ganglion cells

COMP:
- Rupture

RX:
- Resection

75
Q

Alcoholic Liver Disease

Micro Finding, Comp?

A

FINDINGS:
- Mallory bodies

COMP:
- Bilirubin Stones

76
Q

Non-Alcoholic Fatty Liver Disease

Etiology, Assoc, Labs, Comp (2)?

A

ET: Metabolic Sx (Insulin Resistance)

ASSOC:
- Obesity

LABS:
- ALT > AST ** THINK: “L for Lipids” **

COMP:

  • Hepatitis / Cirrhosis
  • HCC
77
Q

Hepatic Steatosis

Def’n?

A

Accumulation of fat (fat droplets) in hepatocytes ->
Heavy + greasy liver.

** May be REVERSIBLE with alcohol cessation **

78
Q

Hepatitis B + C

Conseq?

A

CONSEQ:

- Nephrotic Sx

79
Q

Alcoholic Hepatitis

Def’n, Mediator,
Pres, Micro Findings (CLUE + 1), Labs?

A

Chemical injury to hepatocytes from sustained long-term consumption of alcohol.

MED of damage = Acetaldehyde (metabolite of alcohol).

PRES:
- Painful hepatomegaly

FINDINGS:

  • “Mallory Bodies”
  • Swollen + necrotic hepatocytes with NEUTROPHIL infiltration

LABS:
- AST > ALT **THINK: “Make a toAST with alcohol.” **

80
Q

Alcoholic Cirrhosis

Def’n, Macro Findings (CLUE + 1), Pres?

A

** FINAL + IRREVERSIBLE form of Alcoholic Liver Dz **

FINDINGS:

  • Shrunken liver with “hobnail appearance”
  • Sclerosis around central vein

PRES: Occurs in 10-20% of alcoholics
(Same pres as Chronic Liver Dz)

81
Q

Cirrhotic Liver

Def’n, Chars (2 Histo), Causes (6),
Pres (2 general), Labs (4), Seen In (2),
Comp (3)?

A

END-STAGE liver damage.

CHARS: Destruction of normal liver architecture / parenchyma

  • Diffuse bands of FIBROSIS (mediated by TGF-β from Stellate cells)
  • REGENERATIVE NODULES of hepatocytes

CAUSES:

    • Alcohol
  • a1-antitrypsin def
  • Fructose intolerance (aldolase B def)
  • Viral Hep
  • Hemochromatosis
  • Biliary Dz

PRES:

  • ↓detox
  • Portal Htn

LABS:

  • Ammonia↑
  • Estrogen↑
  • Albumin↓
  • Clotting Factors↓

SEEN IN:

  • Alcoholism
  • Hepatitis B + C

COMP:

  • Hepatocellular Carcinoma
  • Cholesterol Stones
  • 1ry Hyperaldosteronism
82
Q

Cirrhosis #1

Def’n, Chars (2 Histo)?

A

END-STAGE liver damage.

CHARS: Destruction of normal liver architecture / parenchyma

  • Diffuse bands of FIBROSIS (mediated by TGF-β from Stellate cells)
  • REGENERATIVE NODULES of hepatocytes
83
Q

Cirrhosis #2

Causes (6)?

A

CAUSES:

    • Alcohol
  • Fructose intolerance (aldolase B def)
  • a1-antitrypsin def
  • Viral Hep
  • Hemochromatosis
  • Biliary Dz
84
Q

Cirrhosis #3

Pres (4), Labs (4)?

A

PRES:

  • ↓Detox
  • ↓Protein Synthesis (->↓Albumin + Clotting Factors)
    • > Ankle Edema
    • > Anemia / Bleeding tendency
  • Portal Htn
  • Jaundice
    • > Scleral Icterus
    • > Fetor Hepaticus

LABS:

  • Ammonia↑(-> Mental status changes, Asterixis, Coma)
    • Metabolic therefore reversible!*
  • Estrogen↑(-> Gynecomastia, Testicular Atrophy, Palmar Erythema, Spider Angiomata)
  • Albumin↓
  • Clotting Factors↓
85
Q

Portal Htn

Causes, Pres (7)?

A

CAUSES:
- Schistosoma (trematode/fluke) infection

PRES: 
- Esophageal Varices 
  (Shunt: Backup of L gastric vein into the Esoph vein)
     -> Hematemesis
     -> Melena
- Peptic Ulcer
- Splenomegaly
- Ascites / Caput Medusae (Shunt)
- Internal Hemorrhoids (Shunt)

Portosystemic Shunts partially alleviate portal htn

86
Q

Budd-Chiari Sx

Def’n, Causes (2), Pres (3)?

A

Liver INFARCTION due to Hepatic Vein destruction.

CAUSES:

  • RHF
  • Liver Cancer

PRES:

  • Hepatomegaly
  • Ascites
  • Ab pain
87
Q

Nutmeg Liver (Congestive Hepatopathy)

Causes (2), Mech, Assoc (3), Macro Finding (CLUE), Comp (2)?

A

CAUSES:

  • RHF
  • Budd-Chiari Sx

Liver CONGESTION (backup of blood into liver).

ASSOC:

  • Hypercoaguable state
  • Polycythemia Vera
  • Pregnancy

FINDINGS:
- Liver appears mottled like a “nutmeg”

COMP:

  • Cardiac Cirrhosis (due to centrilobular congestion + necrosis)
  • HCC
88
Q

a1-antitrypsin Deficiency

Mech, Genetics, Pres (Liver vs Lung)?

A

Misfolded gene product (protein) AGGREGATES in ER of hepatocytes.

Codominance.

PRES:
- Liver: Cirrhosis with “PAS-positive globules”
- Lungs: Panacinar Emphysema
(due to uninhibited elastase in alveoli -> ↓elastic tis)

89
Q

Hepatitis

Micro Finding?

A

FINDING:

- Mallory Bodies

90
Q

Viral / Toxic Hepatitis

Micro Finding?

A

FINDINGS:

- Councilman Bodies

91
Q

Yellow Fever

Micro Finding?

A

FINDINGS:

- Councilman Bodies

92
Q

Reye’s Sx

Mech, Assoc (2 Micro), Pres (CLUE + 5)?

A

Mitochondrial damage.

ASSOC:

  • Influenza B
  • VZV

PRES = “Child with viral illness who is given Aspirin”

  • Vomiting
  • Hepatomegaly
  • Liver failure
  • Encephalopathy
  • Coma
  • ** Often fatal ***
  • ** Aspirin only recommended for children with KAWASAKI DZ ***
93
Q

Hepatic Encephalopathy

Mech (3 steps), Etiologies (2), Pres (Spectrum), RX (3)?

A

MECH:
Cirrhosis -> Portosystemic Shunts ->↓NH3 metab

ET:

  • ↑NH3 production (eg↑dietary protein, constipation, infection, GI bleed)
  • ↓NH3 metab / removal (eg Renal Failure, Diuretics)

RX:

  • Lactulose (↑NH4 production)
  • Rifaximin (kills intestinal bacteria)
  • Low-protein diet
94
Q

Crigler-Naijar Sx (Congenital UNconjugated Hyperbillirubinemia)

Def’n / Mech, Pres (CLUE), RX (3)?

A

ABSENT UDP-glucuronyl transferase.

PRES = “Severe jaundice in NEONATE”
** Patients die within a few years **

RX:

  • Plasmapheresis
  • Phototherapy
  • Phenobarbital (Type II only)
95
Q

Dubin-Johnson Sx (Congenital Conjugated Hyperbilirubinemia)

Def’n (2 steps), Pres (CLUE)?

A

Def of BRB Canalicular Transport Protein ->
Hepatocytes unable to secrete conjugated BRB into bile.

PRES = “BLACK Liver”

96
Q

Wilson Disease (Hepatolenticular degeneration)

Locations (3 MC + 2), Inher + Genetics,
Pres (Epi +1 Liver + 1 Heme + 4 Neuro),
Micro Finding (CLUE), Labs (2 CLUES: Blood + Urine),
Comp (2), RX?

A
  • Liver
  • Brain (esp Basal Ganglia)
  • Cornea (K-F ring)
  • Kidneys
  • Joints

AR. Chr 13.

PRES: Childhood

  • Fatty change / Hepatitis / Cirrhosis of liver
  • Hemolytic Anemia
  • Asterixis
  • Chorea
  • Tremor
  • Parkinsonian symptoms (Asterixis, Dementia, Dyskinesia, Dysarthria)

FINDING = “Kayser-Fleischer” rings.

LABS:

  • Blood: Ceruloplasmin↓
  • Urine: Cu↑

COMP:

  • HCC
  • Fanconi Sx

RX:
- Penicillamine (chelator)

97
Q

Hemochromatosis (Bronze Diabetes)

Def’n, Causes (2, incl 1 genetic),
Pres (Epi + Triad + 3 Other), Micro Finding, Labs (4 Fe Studies)
DX, Comp (3), RX (2)?

A

Excess body iron -> Hemosiderosis (iron deposition)
-> Hemochromatosis (dz caused by iron dep)

CAUSES:

  • HFE mutation
  • Multiple blood transfusions

PRES: Late Adulthood. “Bronze Diabetes”.

  • ** Iron loss thr MENSES slows progression in women ***
    1. Cirrhosis
    2. DM
    3. Skin pigmentation
  • Arrhythmias
  • CHF
  • Testicular Atrophy

FINDINGS:
- Brown hepatocytes

LABS:

  • Iron↑
  • Ferritin↑
  • % Saturation↑
  • TIBC ↓

DX = Liver Biopsy

COMP:

  • HCC
  • Cardiomyopathy
  • CHF

RX:

  • Repeated Phlebotomy
  • Deferoxamine
98
Q

1ry Hemochromatosis

Def’n, Inher, Genetics (2 possible mutations), HLA Assoc?

A

Defect in iron ABS.

AR.

Mutations on HFE gene:

  • C282Y mutation
  • H63D mutation

HLA-A3 assoc.

99
Q

Jaundice

Def’n, Mech (2 options), Causes (3)?

A

Yellow skin and/or sclerae due to elevated BILIRUBIN (BRB).
BRB > 2.5 mg/dL in blood.

MECH:

  • ↑BRB production
  • ↓BRB metab

CAUSES:

  • Hepatocyte injury
  • Obstruction to bile flow
  • Hemolysis
100
Q

Obstructive Jaundice

Pres (1 + 2 Excretion-Related + 2 Skin-Related), Labs (3)?

A

PRES:

  • Hepatosplenomegaly
  • Dark urine
  • Light stools
  • Jaundice
  • Pruritus

LABS:

  • Conjugated BRB↑
  • Cholesterol ↑
  • Alkaline Phosphatase↑
101
Q

Hemolytic Jaundice

Urine (2: BRB + Urobilinogen)?

A

URINE:

  • BRB ABSENT = Acholuria (absence of bile pigments in urine)
  • Urobilinogen ↑
102
Q

“Painless jaundice”

A

Cancer of the pancreatic HEAD (obstructs bile duct)

103
Q

Liver Cancer (Hepatic Adenoma + HCC)

Assoc (6), Path,
Pres (4), Labs (CLUE + 2),
DX (2 options), Comp?

A

ASSOC:

  • a1-antitrypsin deficiency
  • Cirrhosis
  • Hemochromatosis
  • Hepatitis B + C
  • Wilson dz
  • Aflatoxin (can be produced by Aspergillus species)

Spreads by HEMATOGENOUS dissemination.

PRES:

  • Ascites
  • Jaundice
  • TENDER Hepatomegaly
  • Anorexia

LABS:

  • a-fetoprotein
  • Polycythemia
  • Hypoglycemia

DX:

  • CT
  • U/S

COMP:
- Budd-Chiari Sx

104
Q

Hepatic Adenoma

Assoc (2), Course (2 options)?

A

** RARE **

ASSOC:

  • Anabolic Steroids
  • ↑ Estrogen (ie OCPs or Pregnancy)

COURSE:

  • Regress spontaneously OR
  • Rupture -> Intraperitoneal bleeding (↑risk during Pregnancy)
105
Q

Hepatic Angiosarcoma

Def’n, Causes (3: “VAT”)?

A

Malignancy of Liver. ** Highly lethal **

CAUSES: Exposure to “VAT”:

  • Vinyl Chloride (plastics, rubber)
  • Arsenic (pesticides)
  • Thorotrast (radioactive diagnostic agent)
106
Q

Metastasis to Liver

MC Sources (4), Pres (CLUE + 1)?

A

MC SOURCES:

  • Lung
  • Breast
  • Colon
  • Pancreas

PRES:

  • “Hepatomegaly with NODULAR free edge of liver”
  • Multiple nodules in liver
107
Q

Biliary Tract Disease

Locations w/in Biliary Tract (2), Pres, Labs, Comp?

A

LOCATIONS:

  • INTRAhepatic bile ducts: 1ry + 2ry Biliary Cirrhosis
  • INTRA + EXTRAhepatic bile ducts: 1ry Sclerosing Cholangitis

PRES = (Pres of Obstructive Jaundice)

LABS = (Pres of Obstructive Jaundice)

COMP:
- Cirrhosis

108
Q

Biliary Atresia

Mech (2 steps), Pres (Epi + 1)?

A

Failure to form OR Destruction of Biliary Tree ->
Biliary OBSTRUCTION.

PRES: 1st 3 months
- Jaundice -> Cirrhosis

109
Q

1ry Biliary Cirrhosis

Mech, Assoc, Micro Findings (2), Ab?

A

MECH: AUTOIMMUNE. Lymphocytic infiltrate + Granulomas.

ASSOC = Other Autoimmune conditions.

FINDINGS:

  • Lymphocytic infiltrate
  • Granulomas

AB:
- IgM

110
Q

2ry Biliary Cirrhosis

Etiology, Mech, Causes (4)?

A

ET: EXTRAhepatic biliary OBSTRUCTION

MECH:
↑Pressure in INTRAhepatic ducts -> Injury / Fibrosis
-> Bile Stasis

CAUSES (of extrahepatic biliary obstruction):

  • Biliary stricture
  • Gallstones
  • Chronic Pancreatitis
  • Pancreatic Adenocarcinoma (Head of pancreas)
111
Q

Cholangitis

Pres (Charcot’s Triad)?

A

PRES: Charcot’s Triad

  1. Fever
  2. Jaundice
  3. RUQ pain
112
Q

Primary Sclerosing Cholangitis

Mech, Assoc, Macro Findings (2 steps / CLUES), Ab, Comp (2)?

A

MECH = Infl + Fibrosis.

ASSOC:
- Ulcerative Collitis

FINDINGS: (On ERCP)

  • Concentric “onion skin” bile duct fibrosis ->
  • Alternating strictures / dilations of bile ducts = “beading”

AB:
- IgM↑(Hypergammaglobulinemia)

COMP:

  • 2ry Biliary Cirrhosis
  • Cholangiocarcinoma
113
Q

Ascending Cholangitis

Def’n (incl CB), RF, Pres (2), Comp?

A
BACTERIAL INFECTION (usually ascending) of bile ducts, 
usually with Enteric Gram-Negative bacteria.

RF:
- Bile Duct Stones

PRES:

  • Jaundice
  • Ab pain

COMP:
- Sepsis

114
Q

Cholangiocarcinoma

Assoc (Micro)?

A

ASSOC:

- Clonorchis sinensis (trematode) infection

115
Q

Courvoisier Sign

Mech, Pres (2)?

A

Distal obstruction of biliary tree.

PRES:

  • Obstructive Jaundice
  • Gallbladder distended, palpable, NON-tender
116
Q

Cholelithiasis / Gallstones #1

Causes (3), RF (6: “4 Fs” + 2),
DX (2: Phys Exam + U/S CLUE), RX?

A

CAUSES:

  • ↓Bile Salts (b/c bile salts increase solubility)
  • ↓Phospholipids (ie Lecithin)
  • Gallbladder stasis

RF: “4 Fs”. ** Estrogen **

  • Female
  • Forty
  • Fertile
  • Fat
  • Advanced age
  • Cirrhosis

DX:

  • Phys Exam: Murphy’s Sign
  • U/S: “Air in biliary tree” ONLY in case of fistula or gallstone ileus

RX:
- Cholecystectomy ONLY if symptomatic

117
Q

Cholelithiasis / Gallstones #2

Comp (6)?

A

COMP:

    • Cholecystitis
  • Ascending Cholangitis
  • Acute Pancreatitis
  • Biliary Colic
  • Bile Stasis
  • Fistula b/w Gallbladder + S.I / Gallstone Ileus
118
Q

Cholesterol Gallstones

Appearance, Assoc (8)?

A

Yellow / radioLUCENT with opacities (due to calcifications).

ASSOC:

  • Native American
  • Multiparity
  • Obesity
  • Rapid weight loss
  • Crohn’s
  • Cystic Fibrosis
  • Clofibrate
  • Estrogens
119
Q

Bilirubin / Pigment Gallstones

Appearance, Assoc (2: Micro + 1)?

A

RadiOPAQUE.
** BROWN = Infection. BLACK = Hemolysis. **

ASSOC:

  • Biliary infection (E coli, Ascaris lumbricoides, Clonorchis sinensis)
  • Chronic Hemolysis
120
Q

Pancreatic Disease

Enzymes↑(3)?

A
  • Amylase
  • Elastase-1
  • Lipase
121
Q

Pancreatic Insufficiency

Causes (3), Pres (2), DX?

A

CAUSES:

  • Cystic Fibrosis
  • Pancreatitis
  • Cancer (Obstructing)

PRES: MALABSORPTION with:

  • Fat-Soluble Vitamin def
  • Steatorrhea

DX: D-Xylose Abs Test

122
Q

Acute Pancreatitis

Mech (3 steps), Path (incl 2 types of Necrosis),
Causes (10: “GET SMASHED”),
Pres (3), Labs (3),
Comp (6)?

A

MECH:
Premature activation of Trypsin ->
Activation of other panc enzymes ->
AUTODIGESTION of pancreas by panc enzymes.

PATH: Infl + Hem of pancreas:

  • Liquefactive Hemorrhagic Necrosis of pancreas
  • Fat Necrosis of peripancreatic fat

CAUSES:

  • Gallstones
  • Ethanol
  • Trauma
  • Steroids
  • Mumps
  • Autoimmune dz
  • Scorpion sting
  • Hypercalcemia / Hypertriglyceridemia (> 1000)
  • ERCP
  • Drugs (Sulfa drugs)

PRES:

  • Epigastric ab pain radiating to BACK
  • Periumbilical / Flank hemorrhage (due to necrosis spreading)
  • Anorexia + Nausea + Vomiting

LABS:

  • Amylase↑
  • Lipase↑ * More specific than amylase for pancreatic DAMAGE *
  • Ca↓(Ca consumed during saponification in fat necrosis)

COMP:

  • Pancreatic Abscess
  • Pancreatic Pseudocyst
  • 1ry Hyperparathyroidism
  • ARDS
  • DIC
  • Infection / Shock / Organ failure
123
Q

Chronic Pancreatitis

Causes (3, incl 2 specific to Adults / Kids), Path (4),
Labs (generalization), Imaging (CLUE),
Comp (4)?

A

CAUSES:

  • Alcohol (Adults)
  • Cystic Fibrosis (Kids)
  • Recurrent Acute Pancreatitis

PATH: Damage to pancreatic parenchyma:

  • Chronic infl
  • Calcification
  • Fibrosis
  • Atrophy

LABS: * Amylase + Lipase LESS elevated than in Acute Pancreatitis *

IMAGING: Imaging with Contrast:
- “Chain of lakes” pattern

COMP:

  • Pancreatic Insuf
  • Pancreatic Adenocarcinoma
  • DM
  • 2ry Biliary Cirrhosis
124
Q

Pancreatic Adenocarcinoma

Def’n, MC Location, Markers (2), RF (5),
Pres (3),
RX (3 Therapies), Prog?

A

VERY AGGRESSIVE tumor arising from pancreatic ducts.

MC LOCATION = Pancreatic Head.

MARKERS:

  • CA 19-9
  • CEA (however less specific)

RF:

  • Male
  • African-American or Jewish
  • Age > 50 yrs
  • Tobacco
  • Chronic Pancreatitis

PRES:

  • (Pres of Pancreatitis)
  • Courvoisier’s Sign
  • Trousseau’s Sx

RX:

  • Whipple Procedure
  • Chemotherapy
  • Radiation therapy

PROG = 6 months or less.

125
Q

Splenectomy / Nonfunctional Spleen AUTOSplenectomy

Def’n + MCC, Path, Pres (Epi), Micro Finding (CLUE)?

A

Fibrosis + shrinkage of spleen.
MCC = Sickle Cell Anemia.

↑risk of infection with encapsulated organisms.

PRES = functional splenic dysfunction in early childhood

FINDING = Howell-Jolly bodies

126
Q

Curling Ulcer

Cause, Seen In?

** “Burned by the curling iron” **

A

CAUSE = Severe burns
(Hypovolemia -> Gastric Ischemia -> SLOUGHING of gastric mucosa)

SEEN IN: Acute Gastritis

127
Q

Cushing Ulcer

Cause, Seen In?

** “Always cushion the brain” **

A

CAUSE = Brain Injury /↑ICP
(↑Vagal stim ->↑Ach ->↑digestion / H production)

SEEN IN: Acute Gastritis

128
Q

Virchow Node

Cause, Pres?

A

CAUSE = Abdominal metastasis

PRES = enlarged + hard left supraclavicular node

129
Q

VIPoma

Def’n, Pres, Labs (2 ions)?

A

Non-α + non-β islet cell pancreatic tumor that secretes VIP.

PRES = Copious watery diarrhea

LABS:

  • K↓
  • Cl↓
130
Q

Carcinoid Tumor / Carcinoid Sx

Def’n, MC Locations (3: “AIR”),
Triggers (2), Pres (4 Chars of Carc Sx), Micro Findings, Urine,
RX?

A

Low-grade malignancy
Tumor of neuroendocrine cells of GI tract, esp metastatic S.I tumors.

MC Locations (although can arise anywhere along gut):

  • Appendix
  • Ileum
  • Rectum

TRIGGERS: (stim Serotonin release from tumor)

  • Emotional stress
  • Alcohol

PRES: Carcinoid Sx: carcinoid tumor w mets to LIVER.
(Tumor secretes high levels of Serotonin)
- Flushing
- Wheezing
- Diarrhea
- Carcinoid Heart Dz / R-sided heart murmurs

FINDINGS:
- Dense Core Bodies (tumor grows as a submucosal POLYP-like nodule)

URINE:
- 5-HIAA↑

RX:
- Octreotide

131
Q

Meconium Ileus (Newborn)

Causes?

A

CAUSES:

- Cystic Fibrosis

132
Q

“Megaesophagus + Megacolon”

A

Chagas Dz (Trypanosoma cruzi, Reduviid bug, South America)

133
Q

Fitz-Hugh-Curtis Sx

Def’n, Cause / Assoc, General Pres?

A

Infection of liver capsule.

CAUSE / ASSOC:
- PID

GEN PRES: “Violin string” adhesions of peritoneum to liver