IMS III Flashcards

(322 cards)

1
Q

What disorder is characterized by the phildadelphia chromosome?

A

CML

ber-abl oncogene, translocation of 9&22

blast crisis

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2
Q

What is the best sign of primary myelofibrosis?

A

splenomegaly - the spleen tries to produce cells & enlarges

can cause polycythemia vera

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3
Q

What are the myeloproliferative disorders?

A
  1. Chronic Myelogenous Leukemia (CML)
  2. Primary myelofibrosis
  3. Polycythemia vera
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4
Q

What are myelodysplastic syndromes?

A

bone marrow produces abnormal cells w/o enough healthy cells

  1. Refractory neutropenia
  2. Refractory thrombocytopenia
  3. Refractory anemia
  4. Myelodysplastic syndromes w/ multiple lineage affected
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5
Q

What are the myelodysplastic/myeloproliferative disorders?

A
  1. Chronic myelomonocytic leukemia (CMML)
  2. Atypical chronic myelogenous leukemia (aCML)
  3. Juvenile myelomonocytic leukemia (JMML)
  4. Unclassified
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6
Q

What disorder is characterized by auer rods?

A

Acute Myeloid Leukemias (AML)

20% or more blasts in bone marrow
5 genetic abnormalities

auto/allogenic stem cell transplant

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7
Q

What does the FAB classification tell you?

A

at what point the cell line is affected

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8
Q

Induction vs. consolidation

A

i - high dose of chemo

c - maintenance of chemo

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9
Q

Which WBC disorder is mostly found in kids?

A

ALL - Acute Lymphocytic Leukemia

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10
Q

What is affected in ALL?

A

80% B cell

20% T cell

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11
Q

What is the most common lymphoma?

A

Diffuse Large B-cell Lymphoma

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12
Q

What disorder is characterized by M protein?

A

Plasma Cell Myeloma (Multiple Myeloma)

abnormality of B cells leads to overproduction of M protein
-punched out sternum, urine = Bence-Jones protein

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13
Q

What disorder is characterized by a punched out sternum?

A

Plasma Cell Myeloma (multiple myeloma)

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14
Q

What disorder is characterized by Bence-Jones protein in the urine?

A

Plasma Cell Myeloma (multiple myeloma)

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15
Q

What are the characteristics of multiple myeloma (plasma cell myeloma)

A
  1. M protein
  2. Punched out sternum
  3. Bence-Jones protein in urine
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16
Q

What is T-cell lymphoma/leukemia characterized by?

A
  1. Mycosis fungoides
  2. Sezary syndrome

pruritis & eczematous patches/plaques often on buttocks & thighs

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17
Q

What are the characteristics of Hodgkin’s disease?

A

EBV/HIV

  1. Painful lymph node swelling provoked by EtOH
  2. Reed-Sternberg cells on Bx (owl’s eye)
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18
Q

What is pancytopenia?

A

aplastic anemia with all cell lines affected

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19
Q

Which leukemia is indolent?

A

CLL - Chronic Lymphocytic Leukemia

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20
Q

What happens when mesangial cells contract?

A

in glomerulus

they dec. surface area & dec. GFR

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21
Q

Which part of the loop stimulates renin secretion?

A

Thick ascending limb

senses changes in [NaCl]

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22
Q

Where is the site of action for loop diuretics?

A

Thick ascending limb of loop of Henle

they block the Na, K, & Cl pumps

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23
Q

What hormones act upon the distal convoluted tububle?

A

aldosterone & Ang II - resorb H2O

ANP & urodilatin inhibits H2O resorption

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24
Q

Describe the diff. btwn the principal vs. intercalated cells in collecting duct

A

P - respond to ADH

I - acid/base balance by regulating secretion of acid

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25
Describe the diff btwn diabetes insipidus & nephrogenic diabetes insipidus
d - low ADH from pituitary damage n - collecting tubules unresponsive to ADH -genetic defect large V of dilute urine, severe fluid imbalances
26
How do thiazide diuretics work?
They block Na+ resorption, water follows
27
How do Potassium wasting diuretics work?
they cause K+ excretion, water follows
28
Which disease can progress to ESRD by age 15?
Autosomal recessive cystic kidney disease -chr 6p enlarged kidneys at birth, severe HTN, liver problems
29
What causes the cysts in autosomal dominant cystic kidney disease?
low intracellular [Ca2+] & high [cAMP] most common type of CKD chr. 16, chr 4, PKDIII w/ low GFR, cysts develop in other areas
30
What renal disease is strongly associated w/ tuberous sclerosis?
Angiomyolipoma yellow tumors
31
Which renal disease is usually found during autopsy?
Renal adenoma
32
What are the benign renal tumors?`
1. Renal adenoma 2. Renal oncocytoma 3. Angiomyolipma
33
What benign renal disease is difficult to differentiate btwn renal cell carcinoma?
Renal oncocytoma mahogany-brown tumors
34
What is the most common 1st symptom of malignant renal tumors?
hematuria
35
What is the most common type of renal cell carcinoma?
CA of renal tubular of ductal epithelial cells **clear cell RCC -arises from proximal tubular cells yellow-orange in color
36
What is the most common renal cell carcinoma in kids?
Wilm's tumor
37
What is the tell-tale sign of glomerular diseases?
proteinura
38
What is the biggest cause for ESRD?
Glomerular diseases ---90%!!!
39
What causes glomerular diseases?
immune/inflammatory processes | -hereditary/environmental factors
40
What is the diff. btwn primary & secondary glomerular diseases?
1 - only in 1 kidney 2 - from other diseases, meds ex. Goodpasture syndrome - affects alveoli of lung, SLE, diabetic nephropathy
41
Describe the classifications of glomerular disease
1. Diffuse - all glomeruli 2. Focal - some, not all 3. Global - affecting all parts of glomerulus 4. Segmental - only certain parts of glomerulus 5. Membranous - thickening of capillaries from deposition of IgG 6. Sclerotic - scarring
42
Where are the common sites of deposition for glomerular diseases?
1. Mesangial 2. Subendothelial 3. Subepithelial
43
What is the best sign for nephrotic syndrome?
protein loss >3-3.5g in 24 hours NephrItic is <3g/24h
44
What is the most common primary cause of nephrotic syndrome?
Membranous glomerulopathy the barrier mechanism is gone
45
What is the main cause of nephrotic syndrome in kids?
Minimal change disease - 90% -alteration of podocytes
46
Name the types of glomerulonephritis
1. Acute 2. Post-infectious acute 3. IgA Nephropathy 4. Crescentic 5. Goodpasture syndrome 6. Chronic protein loss <3g/24h
47
What is the most common cause of post-infectious acute glomerulonephritis?
Group A Beta-hemolytic strep (GAHBS) begins 1-2 wks after onset of infection smoky/coffee colored urine
48
Which glomerulonephritis is characterized by lysosomal degradation of the basement membrane?
acute
49
What are the triggers for IgA nephropathy?
URI/GI viral infections IgA deposits in mesgangium most common in developed countries
50
Which glomerulonephritis is characterized by crescent shaped lesions?
Crescentic glomerulonephritis causes: infection/disease/drugs/primary acute onset, decline w/in 6 mo
51
What is goodpasture syndrome?
an autoimmune disorder characterized by a Type II hypersensitivity rxn IgG forms against the basement membrane of the glomeruli & alveoli -SOB & hemoptysis (bc attacks lungs too)
52
Which glomerulonephritis often progresses to ESRD?
chronic glomerulonephritis | -sclerosis & fibrosis of kidney
53
What disruptions does acute renal failure cause?
1. Disruption of fluid, electrolyte & acid/base balance 2. Retention of nitrogenous waste products 3. Inc. serum creatinine 4. Dec. GFR
54
What can acute renal failure lead to?
acute tubular necrosis
55
Describe prerenal acute renal failure
any condition that dec. blood flow to the kidney low GFR, urine Na+, oliguria, high sp. gravity & osmolality
56
Describe postrenal acute renal failure
obstruction w/in the urinary collecting system | inc. P in Bowmann's capsule
57
Describe intrinsic acute renal failure
primary dysfunction of nephrons & kidney itself vascular - dec. renal blood flow, hypoxia, vasoconstriction tubular - inflammation & reperfusion injury, causes casts, obstructs urine flow, tubular back leap
58
If untreated, which acute renal failure disorder can lead to ESRD?
Intrinsic
59
What is the most common cause of acute renal failure in hospitalized patients?
acute tubular necrosis mostly due to sepsis & other organ failure
60
What are the phases of acute tubular necrosis of the kidneys?
1. Prodromal 2. Oliguric 3. Post-oliguric
61
Describe the prodromal phase of acute tubular necrosis
normal or declining urine output, inc. BUN & creatinine during of this phase depends upon cause of injury, amount of toxin ingested, duration & severity of HTN
62
Describe the oliguric phase of acute tubular necrosis
may last up to 8 weeks w/ normal urine output/oliguria, progressive uremia, low GFR, hpervolemia, hyperkalemia
63
Describe the post-oliguric phase of acute tubular necrosis
represents renal recovery, inc. urine output | may last 2-10 days & fully recovered after 1 year
64
What is the GFR requirements for chronic renal failure?
<60mL/min for 3 months loss of nephrons
65
What are the biggest risk factors for chronic renal disease?
**diabetes & HTN kidneys can compensate until 75-80% of nephrons stop working
66
Describe the stages of chronic renal failure
I & II - minimize risk factors III - S/S appear, Tx begins IV - plan for dialysis/transplant GFR <15 mL/min V - transplant or die!!!
67
What type of cells line the esophagus?
stratified squamous epithelium
68
What are the salivary glands?
1. Parotid 2. Submandibular 3. Sublingual
69
What is an atresia?
Abnormal partitioning during development
70
What is omphalocele?
herniation of viscera into base of umbilical cord
71
What is sialadenitis?
a salivary gland disorder caused by an infection
72
What is silalithiasis?
a salivary gland disorder caused by stones/calcifications that obstruct salivary ducts
73
What is Sjoren's syndrome
a salivary gland disorder: autoimmune, destroys exocrine glands **dry eyes, dry mouth
74
What enzymes in saliva prevent bacterial growth?
1. Lysozyme - attacks bacterial cell walls 2. Lactoferrin - chelates Fe 3. IgA binding protein
75
Are a-amylase & lipase deactivated by stomach acid?
a-amylase is, 75% of starches are digested by saliva lipase - hydrolyzes triglycerides
76
What is the esophagus controlled by?
Upper - extrinsic cranial nerves Middle & lower - enteric nervous system
77
What is the pH & cell type of the stomach?
pH - 1-2 simple columnar epithelium
78
What are the function of G cells?
located in the antral epithelium in the stomach induce parietal cells & stimulates release of histamine which also induces parietal cells induces constriction of LES, inc. motility of gall bladder & intestine
79
Where do the proton pump inhibitors act?
on the parietal cells, it uses a proton pump to secrete HCl
80
What do NSAIDS act on in the stomach?
they inhibit prostaglandins prostaglandins inhibit histamine so since histamine is no longer inhibited, it can stimulate HCl secretion
81
What stimulates parietal cells?
1. Gastrin cells 2. Histamine 3. ACh
82
What do parietal cells produce?
1. HCl to digest food | 2. Intrinsic factor for B12 absorption
83
What are common causes of B12 deficiency?
1. Pernicious anemia - autoimmune, destruction of parietal cells 2. Gastric bypass
84
What do chief cells secrete in the stomach?
pepsinogen which is converted to pepsin by HCl to digest proteins
85
What is the function of mucus cells in the stomach?
to protect the lining of the stomach it is alkaline to neutralize the acid
86
What are the Crypts of Lieberkuhn?
glands that secrete ~2L of fluid/day into the lumen of the small intestine if you lose this, you lose goblet cells & endocrine glands
87
What are the layers of the intestinal wall?
1. Serosa 2. Longitudinal muscle - peristalsis 3. Circular muscle - churning 4. Submucosa 5. Mucosa
88
Describe the neural control of the GI tract
1. CNS - autonomic | 2. ENS
89
Describe the CNS control of the GI tract
parasympathetic - stimulates GI tract via vagus nerve sympathetic - inhibits GI activity by NE
90
Describe the ENS control of the GI tract
Myenteric plexus - btwn. muscular layers, stimulation inc. GI activity by Ach Submucosal plexus - w/in submucosa, sensory function, absorption, secretion
91
What hormones influence the GI tract?
1. Gastrin 2. CCK 3. Ghrelin & motilin 4. Secretin 5. Somatostatin 6. Incretins
92
How does CCK act upon the GI tract?
produced by jejunum inc. GB contractility, bile, pancreatic secretion regulates gastric emptying, bowel motility, induces satiety
93
How does ghrelin & motilin act upon the GI tract?
inc. GI motility Ghrelin inc. appetite, rises before meals, falls after dec. levels = satiety causes wt. gain
94
How does secretin act upon the GI tract?
produced by duodenal mucosa in response to gastric juices stimulates pancreas
95
What hormones does somatostatin inhibit in the GI tract?
inhibits: 1. Secretin 2. Motilin 3. Pancreatic function 4. GH short 1/2 life
96
How does incretins act upon the GI tract?
produced in responsed to food inc. insulin dec. appetite short 1/2 life
97
Which hormones induce satiety?
1. High CCK 2. High Amylin 3. High Incretins 4. Low Ghrelin
98
Which nerves are involved in swallowing?
IX - glossopharyngeal X - vagus XII - hypoglossal
99
What induces vomiting?
Nucleus Tract Solitarius - in medulla | input from pharynx, abdomen, labyrinths, Vagus X
100
What is the gastrocolic reflex?
Stimulated by the vagus nerve, causes mass mvmts in colon for pooping
101
What is stomatitis?
inflammation of the oral mucosa
102
What is achalasia & what is it characterized by?
LES does not relax to allow food entry into the stomach **esophagram = bird beak
103
How is scleroderma related to the esophagus?
connective tissue disease that can cause fibrosis of the esophagus
104
What are Schatzki rings?
smooth, circumferential structures in the lower esophagus may be caused by stomach acid
105
What is Zenker's diverticulum?***
pouching of esophagus may be due to loss of elasticity at UES & reduced opening s/s- regurgitation of undigested food, dysphagia, cough, nocturnal choking, halitosis
106
What disease is characterized by pouching of the esophagus?
Zenker's diverticulum***
107
What disorder causes a bird beak on an esophagram?
Achalasia***
108
Who is at risk for infectious esophagitis?
immunocompromised Pts common pathogens: candida, CMV, Herpes
109
What is a DDx for cough?
GERD | Tx: H2 antagonists, PPIs
110
What is Barrett's esophagus?
columnar metaplasia of distal esophagus due to chronic inflammation** Z-line at GE junction risk factor for adenocarcinoma***
111
What esophageal disorder is at risk for adenocarcinoma?
Barrett's esophagus
112
What can chronic inflammation of the esophagus cause?
Barrett's esophagus | -columnar metaplasia of distal esophagus
113
What is a Mallory-Weiss Tear?
a benign condition, VSS*** tear in the esophagus hematemesis usually due to vomiting, retching
114
What disorders can cause abdominal pain but aren't abdominal disorders?
1. MI - common in women 2. Pneumonia - common in kids 3. GU - PID, ectopic pregnancy, testicular torsion, nephrolithiasis
115
What are some causes of constipation?
1. Diet low in fiber 2. Aging 3. Dec. activity 4. Meds 5. Masses 6. Hypothyroidism 7. Diabetes 8. Parkinson's 9. MS
116
What are the 4 different types of diarrhea?
1. Osmotic 2. Secretory 3. Exudate 4. Motility disturbance
117
Describe the physiology of secretory diarrhea
activation of cAMP cycle causes excretion of Cl- into lumen, Na+ & H2O follows ex. cholera, enterotoxins
118
What is gastritis & common causes?
inflammation of the stomach causes: NSAIDS, peptic ulcer disease
119
What is gastroenteritis & common causes?
Inflammation of the stomach & small intestine causes: norwalk virus, N/V/D
120
How is NSAID gastropathy caused?
NSAIDS block COX1 & COX2 causing inc. acid & mucus, causing inflammation & pain
121
What are the different types of peptic ulcer disease?
1. Gastric 2. Duodenal 3. H. Pylori
122
What is gastric peptic ulcer disease & when is it exacerbated?
breakdown of mucosal lining that allows epithelial cells to be exposed to acid worse on empty stomach or immediately after food
123
What is duodenal peptic ulcer disease & when is it exacerbated?
inappropriate acid secretion in pyloric atrum cells worse 2-3 hrs after a meal, food relieves it
124
What percentage of each peptic ulcer diseases does H. pylori cause?
75% duodenal 60% gastric
125
What is the name for the gastrin secreting pancreas tumor?
Zollinger-Ellison syndrome RARE
126
What is the tell-tale sign of Crohn's?
cobblestoning - skip lesions*** chronic granulomatomous lesions
127
Describe Crohn's
disease of small bowel, IBD may extend & form fistulas w/ other organs S/S - diarrhea, cramping, wt loss, eye involvement, arthritis, anemia abs. issues - ferritin, Fe, B12 Cobblestoning - skip lesions
128
What are the different small bowel obstructions?
1. Adynamic ileus | 2. Mechanical ileus
129
Adynamic ileus vs. mechanical ileus
A - dec. intestinal motility, meds, surgery, electrolyte imbalance M - post op. adhesions, hernias, neoplasms, blockage
130
A disease process that has sever pain followed by vomiting is????
mesenteric ischmia | uncommon but deadly! older Pts, occlusion, vasospasm, vasoconstriction of superior/inferior mesenteric artery
131
What are the large bowel disorders?
1. Ulcerative colitis 2. Diverticulitis/diverticulosis 3. Toxic megacolon 4. Large bowel obstruction 5. Pseudomembranous colitis
132
What is the S/S of diverticulitis?
LLQ ab. pain***, fever
133
Describe diverticulitis
herniation through muscles of intestinal wall -from low fiber diet, may be asymptomatic bowel rest, no colonoscopy for 6 wks, high fiber diet, wt loss
134
What are the causes & risks of toxic megacolon?
c - ulcerative colitis, Chron's, infections r - sepsis & bowel perforation
135
What is twisting of the bowel called?
volvulus cecum & sigmoid most common, may constrict blood flow
136
What is telescoping of the bowel called?
Intussusception | excacerbated peristalsis
137
Large bowel obstructions may lead to...?
1. Gangrene 2. Shock 3. Perforation
138
Another name for pseudomembranous colitis?
antibiotic assoc. colitis | = C. Diff!!!!
139
What is a tell-tale sign of IBS?
Mucousy diarrhea****/constipation | NOT IBS = blood, wt loss, fevers
140
What is Hirschsprungs?
congenital -absence of autonomic nerve ganglia, ENS usually affects rectosigmoid region complications - constipation, bacterial growth, diarrhea & enterocolitis
141
Which substances does Celiac cause a dec. absorption?
Fe, B12, folate, Vit D & K --anemia autoimmune
142
What is Whipple's disease?
Very rare bacterial infection, farmer's soil | S/S - steatorrhea, wasting, edema, endocarditis, uveitis, lymphadenopathy, dementia
143
What disease is from a loss of your pyloric sphincter?
Dumping syndrome!!! | small gastric capacity, water pulled into intestine
144
Name the inflammation diseases of GI
1. Stomatitis 2. Esophagitis 3. Gastritis 4. Peptic ulcer disease 5. Crohn's 6. Ulcerative colitis 7. Enterocolitis 8. Diverticulitis
145
Name the motility disorders of GI
1. Achalasia 2. IBS 3. Obstruction 4. Volvulus 5. Intussusception 6. Hirschsprung
146
Name the malabsorption disorders of GI
1. Celiac 2. Dumping 3. Short Bowel Syndrome
147
What are the S/S of esophageal cancers?
wt. loss dysphagia hoarseness
148
Describe squamous cell carcinoma esophageal cancer
most common in old black men, EtOH, tobacco, poor diet
149
Describe adenocarcinoma esophageal cancer
CA of glands | Barrett's esophagus & other high acid states
150
What is a tell-tale sign of gastric cancer?
Epigastric mass***
151
What are the risk factors for colon cancer?
2nd leading cause of CA death, risk doubles every decade IBD, ulcerative colitis, Hx adenomatous polyps, 1st degree relative, tobacco, obesity, diet, high fat, low fiber Familial adenomatous polyposis*** Hereditary non-polyposis colon CA*** watch CEA-125***
152
Describe bile composition
1. Water 2. Electrolytes 3. Bile acids 4. Cholesterol 5. Pigment 6. Phospholipids
153
What is the function of bile?
digestion of lipids/fat | transport waste from liver (bilirubin, IgA, toxins, cholesterol)
154
What are the risk factors of gall stones?
``` Fat Female Fertile Forty FH ```
155
What can gall stones be made of?
70% cholesterol Bilirubin CaCO3 phosphate
156
What is biliary colic?
Transient cystic obstruction
157
What is acute cholecystitis & what is the best sign?
persistent cystic obstruction RUQ pain to R scapula****
158
What is characterized by RUQ pain to the R scapula?
acute cholecystitis
159
What is choledocholithiasis?
cacluli in common bile duct?
160
How do you diagnose cholelithiasis?
US, HIDA scan, CT, MRCA, ERCP
161
What are the complications of cholelithiasis?
gangrene, empyema, cholecystoenteric fistula, biliary peritonitis/sepsis, cholangitis
162
What happens if there is an obstruction in the common bile duct?
cholecystitis & jaundice
163
What happens if there is an obstruction in the sphincter of oddi or hepatopancreatic duct?
pancreatitis
164
What is acalculous cholecystitis?
inflammation of gall bladder w/o gall stones
165
What is primary sclerosing colangitis?
inflammation & fibrosis of the biliary tree may also involve inra/extrahepatic ducts S/S - RUQ pain, jaundice, fevers, wt loss RF - IBD, ulcerative colitis, Crohn's, AIDS, fasciola hepatica
166
Describe biliary malignancy
rare, asymptomatic & insidious until late stages, only about 1/5 are found before they metastasize
167
What are the phases of pancreatic secretion?
1. Cephalic - olfactory & visual signals 2. Gastric - gastrin 3. Intestinal - CCK & Secretin
168
What enzymes does the pancreas secrete?
1. Amylase - carbs 2. Lipase - fat, phospholipase A & lecithinase 3. Proenzymes - protein, trypsinogen & others, inactive until duodenum 4. Bicarb
169
What are the causes of acute pancreatitis?
1. Obstruction of pancreatic duct - digests itself 2. Alcohol 3. Biliary obstruction 4. Hypertriglyceridemia Others: meds, sphinter of oddi dysfunction, idiopathic, infections
170
S/S of acute pancreatitis?
steady & boring epigastric pain N/V Ranson criteria assesses pancreatitis
171
What are the complications of pancreatitis?
1. Necrotizing 2. Pseudocysts - inc. enzymes, needs drained 3. Abscess formation - results in liquefaction & necrosis of pancreatic tissue, collections of pus
172
What is the most common cause of chronic pancreatitis?
chronic alcoholism
173
How do you diagnose pancreatitis?
Lipase - specific, returns to normal w/in 7-14 days Amylase - returns to normal w/in 2-3 days, does not predict severity inc. WBC, triglycerides, bilirubin, ALP, AST, LDH CT abdomen w/ contrast
174
Where in the pancreas is the most cancer found?
``` head 3:1 chance in head than tail 2% of new CA, 4th leading cause of CA death usually mets if showing S/S Dx CA 19-9 ```
175
What are the fat soluble vitamins?
A D E K if liver probs, can't abs these
176
What hormones does the liver metabolize & what problems can liver disease cause as a result?
glucocorticoids & sex hormones men - gynecomastia, impotence, testicular atrophy women - irregular menses
177
What are the functions of cholesterol?
Build & maintain cell membrane, myelin sheath intracellularly - precursor, bile, vit D, steroid hormones 20-25% produced in liver
178
What are the prehepatic causes of inc. bilirubin?
1. Hemolysis 2. Gilberts 3. Sickle cell 4. Crigler-Najarr syndrome
179
What has high serum unc. bilirubin, with no bilirubin and high urobilinogen in urine?
pre-hepatic causes of inc. bilirubin
180
What are the hepatocellular causes of bilirubin problems?
probs getting through biliary tree 1. Liver disease/CA 2. Hepatitis 3. Primary sclerosing cholangitis 4. Dubin-Johnson syndrome
181
What has high serum conj. bilirubin, with high conj. bilirubin with no or little bilinogen in the urine?
hepatocellular or post-hepatic bilirubin problems
182
What are the post-hepatic causes of bilirubin problems?
obstruction - gallstones, pancreatitis
183
Describe the process & causes of cirrhosis?
inflammation to fibrosis to scar tissue & nodules irreversible**** Causes: alcoholism, autoimmune primary biliary cirrhosis
184
What can cause esophageal & periumbilical varices ascites?
Portal HTN
185
What causes hepatic encephalopathy?
an inc. NH4+ from liver disease that crosses the blood-brain barrier
186
What can worsen hepatic encephalopathy?
1. GI bleeding 2. Azotemia/renal failure 3. Constipation 4. Inc. protein intake 5. Hypokalemia 6. Hypoxia 7. Hypercarbia 8. Sepsis 9. CNS depressants Graded: 1-4, 4 is worst (flap)
187
What are the causes of ascites?
1. Cirrhosis 2. CA 3. CHF 4. TB 5. Pancreatitis Tx - Na restriction, diuresis
188
What is hepatorenal syndrome?
renal failure w/o intrinsic kidney disease causes: disturbance of arterial blood flow assoc. w/ portal HTN Tx: hemodialysis
189
What are the causes of fatty liver disease?
1. Alcoholism 2. Non-alcoholic steatohepatitis (NASH) obesity, DM, protein malnutrition, TPN, drugs, rapid wt loss/starvation
190
What is the main cause of liver transplant in the U.S.?
Hepatitis C
191
What are the toxic storage diseases?
1. Hereditary hemachromatosis | 2. Wilson's disease
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Describe hereditary hemachromatosis
abnormal Fe abs. & cirrhosis of liver autosomal recessive, abnormal HFE gene -alcohol inc. risks
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What is Wilson's disease?
Toxic storage disease abnormal deposition of Cu in liver, stripped from ceruloplasmin Kaiser-Fleisher rings in eyes***
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What is Gilbert's disorder?
can't conjugate bilirubin | autosomal dominant
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What disease is characterized by Kaiser-Fleischer rings?
Wilson's disease
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What are the S/S & causes of liver abscesses?
S/S - fever, RUQ pain c - portal vein infection, ascending cholangitis, bacteremia
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What are the causes of a hepatoma?
hep B & C, cirrhosis, hemachromatosis mostly metastatic
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What hormone is derived from tyrosine amines?
Catecholamines water sol, faster acting
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What are the different cell membrane receptors?
1. G-linked | 2. Protein kinase
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Which hormones use a protein kinase receptor?
1. Insulin 2. GH 3. Prolactin
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Define permissiveness
inc. # of receptors for a diff. hormone to inc. response | ex. thyroid hormone & E
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Specificity vs. affinity
fit | tightness
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Describe the structure of the adrenal & which hormones are produced
1. Medulla - NE & E 2. Reticularis - steroids & androgens 3. Fasciculata - cortisol 4. Glomerulosa - aldosterone
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Growth hormone is inc. when??
night!
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Acromegaly is caused by?
inc. GH peaks in 4/5th decade also assoc. w/ diabetes due to effect of GH on liver
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What is Grave's disease?
autoantibodies stimulate TSH receptors on thyroid inc. T3&T4...causes goiter this dec. TSH from neg. feedback causes exophthalmos from autoimmune injury to eye
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What is Hashimotos?
Most common cause of hypothyroidism aka lymphocytic thyroiditis autoimmune causing dec. T3&T4
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What is Addison's?
Primary insufficiency | Dec. cortisol from autoimmune destruction of adrenal cortex
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What is secondary insufficiency of cortisol?
inadequate secretion of ACTH from APG
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What is tertiary insufficiency of cortisol?
dec. CRH secretion from hypothalamus
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What are S/S of dec. cortisol?
electrolyte imbalances (hyponatremia), weakness, malaise, hyperpigmentation of skin
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Why does dec. cortisol cause hyperpigmentation of the skin?
there is no neg. feedback of ACTH production so it stimulates melanocytes & promotes pigmentation
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What is inc. cortisol called & S/S?
Cushings caused by adenomas of adrenal cortex (1) or pituitary (2) S/S - stretch marks (ab. striae), dorsocervical fat pad & kyphosis (buffalo hump), large, round, ruddy face (moon faces)
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What is pheochromocytoma?
a tumor that causes excessive production of catecholamines (NE & E) secondary cause of HTN if they complain of HA, tachycardia, diaphoresis***
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What happens to Ca in hyperparathyroidism & what is the common cause?
inc. adenoma S/S - Stones, Bones, Ab. Groans (pancreatitis) & Psychological Moans
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What are nociceptors stimulated by?
- direct damage to nerve endings or release of chem. at site of injury 1. Histamine 2. Serotonin 3. Bradykinin 4. Prostaglandin
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What types of fibers transmit nociception signals?
1. A delta | 2. C fibers
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A delta fibers vs. C fibers***
nociceptors transmission A - myelinated, very fast transmission, sharp, stinging & highly localized, provide specific info. about pain location w/ minimal emotional involvement C - unmyelinated, dull, aching, poorly localized, assoc. w/ aversive emotional response
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Why do people experience referred pain?
afferent nerve fibers enter the spinal cord via posterior nerve roots in the lamina the lamina V has somatic & visceral fibers
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What is a dermatome?***
an area of the body surface, each spinal nerve contains nociceptive fibers for each area
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Which neurotransmitter is involved in synaptic memory?
Glutamate has an excitatory effect, binds w/ NMDA receptors when C fibers are repeatedly stimulated, they become sensitized & mild stimuli can be painful (chronic pain syndromes)
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What factors can influence perception?
fear, fatigue, anxiety, previous experiences, etc.
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Pain threshold vs. tolerance
Theshold - level of painful stimulus required to be percieved Tolerance - degree of pain that one is willing to bear before seeking relief
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Why do some people rub/shake a painful area after injury?
stimulation of large touch neurons can inhibit transmission of nociceptor impulses
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What are the naturally produced opioids?
1. Endorphins | 2. Enkephalins
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What are the types of opioid receptors?
1. Mu 2. Kappa 3. Sigma 4. Delta Mu & Kappa have analgesic effects The other effects account for narcotic side effects - constipation, pruritis, N/V
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What drugs are used to reverse a narcotic overdose?
Naloxone & naltrexone opioid antagonists
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What is physiologic pain?
tissue is injured, pain is preventative for further injury ex. touching a hot stove
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What is pathologic pain?
occurs after tissue injury changes in somatosensory pathways 1. Hyperalgesia 2. Allodynia
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What is hyperalgesia?
significantly enhanced pain sensations type of pathologic pain
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What is allodynia?
non-noxious stimuli causes pain type of pathologic pain
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Acute vs. chronic pain
A - result of direct tissue injury, resolves when injury heals, usually 3 months, pain is self-perpetuating
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What is neuropathic pain?
Nerve injury, GABA inhibitory neurons depleted, hyperalgesia & allodynia, burning shock-like pain can be disabling & difficult to manage Ex. trigeminal neuralgia, diabetic neuropathy, postherpetic neuralgia
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Describe diabetic neuropathy
inflammation/destruction/demyelination of larger peripheral nerves loss of inhibitory input & unopposed nociceptive input, burning pain in "stocking-glove" distributions, fine touch & vibratory sensation lost
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What is intermittent claudication?***
chronic ishemic pain, intermittent, atherosclerotic, crampy quality relieved w/ rest
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What are the 4 mechanisms of pain mgmt?
1. Interrupt peripheral transmission (ex. NSAIDS, ice) 2. Modulate pain transmission at the spinal cord (ex. massage, acupuncture) 3. Spinal cord intervention (ex. epidural) 4. Alter perception of pain (ex. opioid analgesic)
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Where is the CSF contained?
subarachnoid space - btwn arachnoid & pia mater
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What is an epidural hematoma?
bleeding btwn the dura mater & skull usually from tear of arteries
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What is a subdural hematoma?
bleeding btwn dura & arachnoid mater usually from traumatic injury
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What is an arachnoid hemorrhage?
bleeding in subarachnoid space (btwn arachnoid & pia mater) usually caused by cerebral aneurysm Pts complain of thunderclap headache
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What is wrong when someone complains of a thunderclap headache?
arachnoid hemorrhage***
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What is hydrocephalus?***
if there is a blockage & CSF keeps being produced causing inc. size of the ventricles
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What is it called when someone loses the ability to produce language?
Broca's aphagia***
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What is Wernicke's area?***
ability to comprehend language Brodmann areas 39, 40 & 22 loss of this = receptive aphasia
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What is global aphasia?
Broken Wernicke's & Broca's area loss of ability to produce & comprehend language
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Which lobe is associated with societal behavioral norms?
frontal love
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Which system deals w/ memory, emotion & smell?
limbic system
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Which basal ganglia is associated with OCD?
Caudate nucleus dec. activity = depression, schizophrenia
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Which basal ganglia is associated with Tourettes?
Putamen
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Which basal ganglia is associated with Parkinson's?
Substantia nigra***
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Name the basal ganglia
1. Caudate nucleus 2. Putamen 3. Globus pallidus 4. Subthalamus 5. Substantia nigra
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Name the parts of the diencephalon
1. Thalamus - relay center 2. Hypothalamus/pituitary 3. Pineal gland
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What does cerebellar dysfunction lead to?
1. Ataxia - balance disturbance 2. Intention tremor 3. Past pointing in finger-nose-testing 4. Dysdiadochokinesia - failure of rapid alternating movements
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Intention tremor vs. Parkinson's
I - no tremor at rest but as they reach toward target the tremor inc. P - tremor at rest, resolves as they approach target
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What is decussation and where does it occur?***
crossing over of sensory & motor tracts occurs in medullary pyramids
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Where is swallowing, vomiting, coughing & sneezing regulated?
medulla oblongata also decussation
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Name the sensory tracts
ascending 1. Dorsal column-lemniscal tract 2. Anterolateral spinothalamic tract
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Describe the dorsal column-lemniscal tract
sensory ascending tract fine touch, vibration, proprioception runs ipsilateral & crosses over in medulla lesion above medulla - contralateral defecit lesion below medulla - ipsilateral defecit
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Describe the anterolateral spinothalamic tract
sensory ascending tract pain, itch, temperature crosses over at spinal level
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What does the Romberg test measure?
proprioception | needs vision & vestibular system to maintain
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Name the motor tracts
``` descending 1. Corticospinal Extrapyramidal tracts 2. Rubrospinal 3. Reticulospinal 4. Tectospinal 5. Vestibulospinal ```
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Describe the corticospinal tract
motor descending tract anterior & lateral majority crosses over in medullary pyramids coordinate mvmt of extermities
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What do the extrapyrimidal tracts control?
Proximal muscles including the axial skeleton & facial expressions Areas involved: cerebellum, substantia nigra, red nucleius, reticular nucleus & vestibular nuclei
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Give an example of an extrapyrimidal disoder
Parkinsons*** deterioration of the dopaminergic neurons in the substantia nigra impaired motor function w/ tremor & bradykinesia "masked facies" dec. dopamine, treat w. COMT inhibitors & MAO inhibitors
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What is the neurotransmitter for preganglionic neurons?
ACh***
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What is the neurotransmitter of postganglionic neurons?***
SNS - NE sweat glands & some skeletal muscle - ACh alpha 1, 2, B 1, 2, 3, DA receptors PSNS - ACh skeletal muscle - nicotinic ACh receptors organs - muscarinic ACh receptors
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What is the function of astrocytes?
blood-brain barrier
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What is the function of oligodendrocytes/Schwann cells?
form myelin sheath***
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What is the function of ependymal cells?
line ventricles & central canal of spinal cord, producing CSF & maintaining CSF-brain barrier***
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What is myasthenia gravis?***
an autoimmune disorder that causes destruction of nicotinic receptors muscle weakness in eyes 1st
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What are the ACh receptors?
Nicotinic - ionotropic, direct effect on ligand gated channels Muscarinic - metabotropic, 2nd messenger action, usually G protein
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What is dopamine degraded by?
COMT & MAO inhibit this in Parkinson's
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What are the neurotransmitters?
1. ACh 2. Dopamine 3. NE 4. Serotonin 5. Glutamate 6. GABA
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What is glutamate & what is the receptor?
excitatory neurotransmitter*** memory high doses - may be neurotoxin NDMA receptors
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What is the excitatory neurotransmitter?
glutamate
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What neurotransmitter is associated with depression?
serotonin - low levels
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What is an inhibitory neurotransmitter?
GABA*** barbituates & benzodiazepines inc. GABA activity causing sedation & depression
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How is glucose taken into the cell w/ insulin?
GLUT4 receptors in muscle & adipose
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What hormones are produced in the Islets of Langerhans in the pancreas?
B - insulin + amylin a - glucagon delta - somatostatin
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What does amylin do?
peptide hormone produced by beta cells w/ insulin | inhibits gastric emptying, induces satiety, suppresses glucagon
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Describe Type I diabetes
destruction of beta cells in pancreas = no insulin! | autoimmune
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S/S of diabetes?***
1. Polyuria 2. Polydipsia 3. Polyphagia
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What disease has Kussmaul's breathing?
hyperventilation diabetic ketoacidosis
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S/S of ketoacidosis
N/V, ab pain, wt loss, weakness/malaise, lethargy, fatigue, hypovolemia & dehydration hypokalemia*** hyponatremia, inc. anion gap
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Describe Type II diabetes
1. Insulin resistance 2. Lack of insulin from beta cell burn out absent 1st phase spike, dimished second phase retinopathy - occurs in phases
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S/S of type II diabetes
1. Polyuria 2. Polydipsia 3. Unexplained wt loss 4. Frequent UTIs*** 5. Frequent yeast infections 6. Paresthesias
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Which diabetes med is good for fat people?***
Metformin - may experience wt loss inhibits hepatic gluconeogenesis
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What diabetes med is good for skinny people?***
Sulfonylureas stimulate beta cells to inc. insulin production
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What med decreases peripheral insulin resistance?***
Thiazolidinedione (TZDs)
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Somogyi effect vs. Dawn phenomenon
S - low blood sugar in am - dec. pm insulin D - high blood sugar in am - inc. pm insulin
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What should you test with your diabetic Pts?
HbgA1C q 3 months annual dilated eye exam foot care
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Which disorder has Reed-Steinberg cells?
Hodgkin's lymphoma
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If you have Familial adenomatous polyposis, what do you have an inc. risk of?
Colon cancer
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Clinical dehydration is a combination of what two disorders?
1. ECF Volume defecit | 2. Hypernatremia
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What is excess volume in the interstitial compartment called?
edema
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Which electrolytes are higher inside the cells?
K, Mg, PO4
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Which electrolytes are most important in the body?
1. Na 2. K 3. Ca 4. Mg 5. Cl 6. HCO3 7. PO4
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Which electrolyte is most important for the RMP?
K
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Why does hypocalcemia cause hyperexcitability?
Na channels left open with hypercalcemia the Na channels are closed so there isn't any depolarization
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Why does hypomagnesia cause inc. excitability?
inc. in ACh caused by alcoholism
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Name the buffers in the blood
1. Bicarb - in ECF 2. Phosphate - in ICF & urine 3. Hgb - in erythrocytes 4. Protein - ICF & blood
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What does the blood pH need to stay between?
6. 9<7.8 | 20: 1 ratio of bicarb to carbonic acid to maintain normal pH
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What is the renal compensation of low pH?
excretion of NH4+ b/c H+ binds and can get rid of acid
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What is the renal compensation of high pH?
excrete HCO3- & dec. secretion of NH4+
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What ion reflects the effectiveness of renal regulation of metabolic acidosis?
bicarb if low bicarb, more bound to buffer b/c more acids in blood
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What type of lymphoma can develop into diffuse large B cell lymphoma?
Follicular lymphoma Indolent course
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What lymphoma is common in the GI tract?
MALT
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Which virua is associated with Burkitt's lymphoma?
EBV
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Which lymphomas are associated with HIV?
1. Diffuse Large B-cell 2. Burkitt's 3. PCNSL 4. Hodgkin's
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What type of nephrons create concentrated urine?
Juxtamedullary - longer loop of Henle create renin
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Which disease shows smoky or coffee colored urine?
Post-infectious acute glomerulonephritis from GABHS
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What are some reasons for starting dialysis?
ATN or CKD in stage 5 to remove metabolic wastes, correct fluid & elecrolyte abnormalities GFR ~ 15 mg/dL development of uremia & hyperkalemia
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visceral vs. somatic pain
v - diffuse, poorly localized, collicky s - localized & continuous
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What hormones decrease the effects of insulin?
1. Glucagon 2. Cortisol 3. GH (inc. peripheral insulin resistance) 4. Catecholamines
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What can Norwalk virus cause?
Gastroenteritis also can be caused by N/V/D
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Descibe colon cancer surveillance
CEA-125 q3mo for 2 yrs, q6 mo up to 5 yrs Colonoscopy - 1 yr, 3yrs, then 5yrs US/CT abdomen (liver) q6 mo for 3 yrs
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How long does it take for jaundice to occur with hepatitis A?
5-7 days*** no longer contagious after jaundice
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Which hormones stimulate the pancreas?
1. CCK 2. Secretin 3. Incretins (insulin, inhibits glucagon)
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Which hormones stimulate motility in the GI tract?
1. CCK 2. Ghrelin 3. Motilin
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Which hormones affect gastric emptying?
1. Amylin - inhibits | 2. CCK
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If a Pt has HTN & has a HA, tachycardia & diaphoresis, what could it be?***
pheochromocytoma autoimmune disorder where you produce too much NE & E
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Which hormones affect the gall bladder?
1. CCK | 2. Gastrin