cps bingo!
TRANSCRIPT
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CPS Bingo!April 13, 2010
Presenter: Erin Snyder, MD
B5Today’s speaker has no conflict of interest to disclose.
The University of Alabama School of Medicine is accredited by the Accreditation Council for Continuing
Medical Education to provide continuing medical education for physicians.
UAB School of Medicine designates this educational activity for a maximum of 1 AMA PRA Category 1
Credit (s) Physicians should only claim credit commensurate with the extent of their participation in the
activity.
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Case 1
58 year old African American Male presents to VA ER with AMS
Alternately agitated and somnolent
C/O pain all over when he is awake enough to respond to questions
Followed at VA in Tuscaloosa, Remote Data is “down”
Family not present
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Physical Exam
Vitals: 98.2, 185/90, 95
Somnolent, slow to respond, sitting in bed, eyes closed, no acute distress
Eyes: PERRLA, EOMI
Neck: no JVD, no lymphadenopathy/thyromegaly
Chest: clear bilaterally, diffuse chest wall TTP
CV: RRR without murmur
Abd: soft nontender
Extremities: no edema, no clubbing, +2 pulses
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Data
141 102 28
4.3 29 1.6
8.411.4
32.8176
CK: 146, MB: 2, troponin 0.188
EKG: +LVH, Q waves in II, III, AVF, no acute ST changes
UDS: negativeAmmonia: 20TSH: 1.80RPR: negativeHIV: negative
184Ca: 14.6Mg: 2.1PO4: 4.4
LFTs: Normal
UA: trace protein, 4+ glucose, 1+ blood, 6 RBC, <1 WBC
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More Data
PTH: 7.3 (15-65)PTHrP: 16 (14-27)
SPEP: normalSerum IFE: not done
UPEP: 2 bands c/w paraproteinUrine IFE: + free Kappa Light Chains
Bone Marrow Biopsy: monoclonal plasma cell population c/w multiple myeloma
CT Chest/Abdomen/Pelvis: innumerable lytic lesions
throughout vertebral column, sternum, and medial iliac bones
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Hypercalcemia: Differential Diagnosis
Hyperparathyroidism Often chronic, asymptomatic, normal physical
exam
Malignancy PTHrP: squamous cell carcinomas, renal,
bladder, breast, ovarian, lymphomas, leukemias
Osteolytic metastases: multiple myeloma, breast, lymphoma
Ectopic PTH: Ovarian, lung, pancreatic
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Granulomatous Disease: TB, sarcoid
Vitamin D intoxication
Medications: Thiazides, lithium, theophylline
Etc: Hyperthyroidism, Adrenal Insufficiency, pheochromocytoma, milk alkali syndrome, immobilization, TPN
Hypercalcemia: Differential Diagnosis
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Hypercalcemia: evaluation
Check PTH
Elevated or
High NormalLow
Primary
Hyperparathyroidism
Familial
Hypocalciuric
Hypercalcemia
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Low PTH
PTHrP Vitamin DSPEP/UPEP
IFETSH
1,25 OH
Vitamin D high:
Granulomatous
Disease
25 OH
Vitamin D high
ingestion
Hypercalcemia: evaluation
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Multiple Myeloma
Approximately 1% of cancers in US
Men>Women (1.4:1), Blacks>Whites>Asian
Median age at diagnosis 66
Proliferation of a clone of plasma cells producing a monoclonal immunoglobin
Present with: anemia, hypercalcemia, bone pain, protein gap, acute renal failure
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Multiple Myeloma: diagnosis
SPEP/UPEP detects monoclonal band, IFE determines type Sensitivity of SPEP= 82%
add IFE = 93%
add UPEP and urine IFE= 97%
Urinalysis: Myeloma casts, negative protein
Peripheral Smear: rouleaux, leukopenia, thrombocytopenia
Bone marrow biopsy: usually >10% plasma cells
Skeletal survey: Chest, CTL spine, Pelvis, Skull, humeri, femora, any symptomatic areas 80% have lytic lesions, diffuse osteopenia, or fractures
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Case 2
49 year old African American Female
Chief complaint: Hematuria
Intermittent x2 days
Painless
No dysuria
Never happened before
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Past Medical History
Frequent urinary tract infections
Hospitalization for urosepsis 2006
Hypertension: on HCTZ since 2006
Pulmonary Thromboembolism 2002
“one time, the ER told me I had a kidney stone”
Incidental finding when she was there for headache
CT angio of chest showed renal stones, urine was infected
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Family History
Both parents died with CAD in their 70s
Sister alive with HTN
No family with renal disease or kidney stones
No sickle cell disease or sickle trait
Social History
Patient works as PCT at UAB
has one daughter, healthy.
Drinks a few times a year
Never smoked, no illicit drug use
More History
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Review of Symptoms
No fever, chills, weight changes
No nasal congestion, pharyngitis, rhinorrhea
No abdominal pain, nausea, vomiting, diarrhea, rectal bleeding
Post-menopausal: No period in a year, intermittent hot flashes, not worse
No change in exercise/activity level
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Physical Exam
142/85, 79, temperature 97.3, weight 151.
General, HEENT, CV, Lungs all benign
Abdomen: soft, non tender, NABS, no hepatomegaly
No CVA or suprapubic tenderness
GU: Adenexa non-palpable, non-tender, Uterus small, firm, non-tender
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Data
141 104 9
3.6 29 0.8110
5.7
13.6
42
318PTT 30PT 14, INR 1.07
UA: red, pH 6.0, specific gravity 1.0173+ blood, 1+ ketones, 2+ LE, +nitrite, 3+ protein, - Glucose>25 RBC, 6-10 WBC, Many bacteriaNo casts
Renal US: Normal size kidneys, Right renal calculi with moderate right hydronephrosis
CT Abdomen: Moderately severe right hydroureteronephrosis, multiple stones in the right lower pole collecting system. Delay in contrast excretion into the right collecting systemA small amount of the air in the right collecting system.
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Resolution
Urology referral
Cystoscopy normal
Renal scan with mild delay, consistent with UPJ obstruction
OR Laparoscopy, ureteral stent placement, stone removal
26 Calcium Oxalate stones removed from collecting system
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Red Urine
Examine Urine
Sediment
- Red Cells + Red Cells
GlomerularExtra-
glomerularHemoglobinuria/
Myoglobinuria
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Gross Hematuria:Differential Diagnosis
Extraglomerular Glomerular
Renal Mass Post streptococcal glomerulonephritis
Vascular: AVM, renal artery/vein thrombosis
IG A Nephropathy
Loin-pain hematuria syndrome Thin basement membrane disease
Polycystic Kidney Disease Inherited disease: Alport syndrome, Fabrydisease, sickle cell nephropathy
Nephrolithiasis Analgesic nephropathy
Bladder disease: schistosomiasis, bladder mass, cystitis
Prostate disease
Urethritis
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Extraglomerular Hematuria: Evaluation
Urine Cytology
Sensitivity 40-76% for bladder cancer
Imaging
CT urography: pre and post contrast imaging
Less sensitive: IVP, US, MRI
Cystoscopy
If negative
Low risk patients (young, transient hematuria): consider periodic urine cytology
High risk (>50 yo, persistent hematuria): q6-12 month imaging (US), urine cytology, possibly repeat cystoscopy at 1 year
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Stone prevention
Increase fluid intake: increases urine flow rate and decreases urine solute
Decrease animal protein, increase fruit/vegetable intake: decreases urine calcium, uric acid and increases urine citrate
Limit dietary oxalate: spinach, rhubarb, peanuts, cashews, almonds
Low Sodium diet: increases calcium reabsorption in proximal tubule
Normal calcium intake:
Less calcium absorbed from intestine increased oxalate absorption and excretion = enhanced stone formation
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Stone Prevention: medication
Check 24 hour urine for calcium, protein, creatinine, uric acid, oxalate, citric acid, pH
Hypercalciuria: thiazide
Hyperuricosuria: Allopurinol
Hypocitraturia or low pH: Potassium citrate
For calcium phospate/ calcium oxalate stones: check serum calcium and PTH
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Case 3
30 year old White Female
Chief complaint: “Worst headache of my life”
Presentation: sudden onset 2 days ago
Quality: sharp pain
Severity: “Worst headache of my life”
Timing: Intermittent x2 days
Better with: dark room
Worse with: light, noise, activity
Associated findings: nausea, photophobia
Noted light-headed, dizzy, blurred vision with exercise recently
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Past Medical History
Migraines
This HA is different
Usual migraine meds don’t help
Depression
Medications
OCPs
Prozac
Zolmatriptan prn
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More History
Family History
No aneurysm
No Polycystic Kidney Disease
Social History
Single, two children
No tobacco, ETOH, illicits
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Physical Exam
Vitals: AF, 144/90- improves to 120/90 in the room
HEENT: sharp optic disc, fundi normal, EOMI, CN intact
Neck: no meningismus, no lymphadenopathy
CV, lung, abd all normal
Neuro: 3+ symmetric DTRs, otherwise normal
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Evaluation
CT head: L cerebellar infarct
MRI brain: Left vertebral artery dissection
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Headache
Migraine
Cluster
Tension
Medication Overuse headache
Mass: pseudotumor, CNS tumor, meningeal tumor
Infection: meningitis, CNS abcess
Bleeding: Subarachnoid hemorrhage, Subdural hematoma, AVM, aneurysm/dissection
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Migraine
Unilateral (60-70%) or bilateral
gradual onset, crescendo pain pattern
Throbbing pain
Worse with activity
Associated with nausea, aura, photophobia, phonophobia
Lasts 4-72 hrs
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Cluster Headache
Always unilateral, usually around the eye
Begins quickly, quick rise to peak
Explosive, deep, continuous pain
Associated with lacrimation, eye redness, rhinorrhea/nasal congestion, sweating, sensitivity to alcohol
Lasts 30 minutes to 3 hrs, may recur at same time of day for several days/weeks at a time, then remit
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Tension Headache
Usually bilateral
Pain waxes and wanes, described as tightness, stiffness
Duration variable, often at end of the day
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Headache danger signs
Sudden onset, reaches maximal intensity in seconds/minutes
First or Worst Headache
Worsening headache pattern
Neurologic symptoms, other than aura
Mental status changes
Fever
Association with exercise, minor trauma
New headache in: <5 or >50, cancer, HIV, pregnancy, postpartum
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Cervical artery dissection
Headache most common presenting sign 60-95% of carotid dissection
70% of vertebral dissection
Unilateral (same side as dissecting artery)
Often with neck pain, especially with carotid dissection
Associated signs: Horner’s syndrome, amarosus fugax, diplopia, TIA, pulsatile tinnitus
In absence of stroke, CT head not diagnostic MRI/MRA, CTA, ultrasound (need skilled operator)
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References
Up To Date 17.3
Mazhari R, Kimmel PL. Hematuria: An algorithmic approach to finding the cause. Cleveland Clinic Journal Of Medicine. 2002; 69(11): 870-884
Portis AJ, Sundaram CP. Diagnosis and initial management of kidney stones. American Family Physician. 2001;63(7): 1329-1338
Kourambas J, et al. Role of stone analysis in metabolic evaluation and medical treatment of nephrolithiasis. J of endourology. 2001;15(2): 181-186
Debette S, Leyes D. Cervical-artery dissections: predisposing factors, diagnosis, and outcome. Lancet. 2009; 8: 668-678.
Tramontina, Gary. Alabama’s Bingo Halls. New York Times.http://www.nytimes.com/slideshow/2009/11/12/us/1112BINGO_index.html