Title: Nephrology Case Presentation
1Nephrology Case Presentation
- Staci Smith DO
- November 20, 2009
2Case Presentation
- 55 yo CM with CKD 3 ( baseline Cr 1.5-1.8)
presents to GVH ER with nausea , vomiting, and
inability to keep liquids or any medicines down
since surgery last Friday. Pt noticed that his
abdomen has become progressively larger . He has
not been passing flatus or had any recent BM. - Pt has been hypotensive with sbps in the 90s
- NG tube was placed in the ER with 1800 cc of
green liquid output returned immediately.
3Pertinent Review of Systems
- Positive for fatigue, decreased appetite and po
intake, increased abdominal girth as well as ab
pain (now 10/10) - Decreased BMs and flatus
- Renal / Urinary specific
- Chronic foamy urine
- Positive bilateral renal carcinoma
- Decreased urinary output for past two days
- No recent OTC NAIDS
- No gross hematuria, known UTIs, recent contrast
or colonic prep, incontinence, bph, history of
stones, need for any dialysis
4Outpatient Medications
- 1.Lisinopril / HCTZ 20 /12.5 one daily. 2.
Glyburide 5 mg twice a day. 3. Neurontin 300 mg
three times a day. 4. Aspirin 81 mg daily. 5.
Multivitamin one p.o. daily. 6. Lantus 50 units
subcutaneous p.m plus sliding scale insulin - 7. Norvasc 10 mg daily. 8. Coreg 25 mg twice a
day. 9. Plavix 75 mg daily. 10.Crestor 20 mg
p.o. every p.m. 11.TriCor 145 mg daily
5Past Medical History
- 1. CKD 3 - baseline Cr 1.5-1.82. Bilateral renal
masses, worrisome for renal cell carcinoma3.
Hypertension 4. Coronary artery disease5.
Hypercholesterolemia - 6. MI 7. Peripheral vascular disease
- 8. Diabetes mellitus, type 2, insulin requiring
9. Tobacco abuse
6Patient History
- Past Surgical History
- 1. Right partial nephrectomy at OSU a week ago
2. He has had heart catheterization with PTCA.
3. Lipoma removal on the scalp. 4. Left lower
extremity angioplasty in 2006 - Allergies
- none
- SHx
- Only positive for tobacco abuse x 30yrs, but quit
one week ago - FHx
- No family members on HD or immediate family with
cancers - Positive family history of DM and HTN
7Important History
- Notably, the pt has a history of bilateral renal
masses since April 2009 - Partial right nephrectomy at OSU last Monday
- Previous poor outpatient follow up since April
2009 - Seen at Cassano Nephro only once in initial
consult - Multiple phone calls to stress importance of
timely follow up
8ER Physical Exam
- VS BP 106/92- 92 HR, 96.7 F,15 RR, 95 on 2L
oxygen - Gen Appears uncomfortable no acute distress
- HEENT Atraumatic, normocephalic. EOMI. Sclerae
anicteric. Mucous membranes are dry - CV HRR without murmur, rub, click, or gallop.
S1, S2 - Pulm CTAB without wheezing,rhonchi, or crackles
- Ab Distended. Positive bowel sounds. He does
have lap trocar insertion site with mild
erythema, and his belly has voluntary guarding. - Ext No clubbing, cyanosis, or edema. No calf
tenderness bilaterally. Distal peripheral pulses
are 2/4. No Lindsays nails - Neuro There is no asterixis. CN 2-12 GI
9ER Initial Labs
- 134 88 49 172
- 3.5 34 6.1
- No Ca, Mg, Phos, UA
- 20.5 15.0 474
- 46.3
- Cr back in Oct 2009 1.5
-
10ER Initial Labs
- CT scan without contrast
- high-grade small bowel obstruction at the level
of the ventral hernia - large amount of subcutaneous emphysema, small
amount of retroperitoneal and smaller amount of
intraperitoneal gas regional to the right kidney
where there has been recent surgical
intervention
11Cause of the Patients Acute Kidney Injury ?
- Multifactorial
- hypovolemia
- Secondary to GI loss with nausea and vomiting
- Poor po intake with outpatient diuretics (HCTZ)
- hypotension in the prescence of OP ACE-I
- Bp 90/46 in ER
- rule out urinary obstruction
- nurses unable to place Foley
- can bladder scan
12What is Acute Kidney Injury?
- An abrupt reduction in kidney function within 48
hours - absolute increase in serum creatinine of gt 0.3
mg/dl - a percentage increase of 50
- a reduction in urine output
- documented oliguria of lt 0.5 ml/kg/hr for gt 6
hours - realize that acute kidney injury may be a
precursor to CKD, and CKD can also lead to AKI
13Stages of AKI
Stage Cr Criteria Urine Output Criteria
1 ? Serum Cr of gt0.3 mg/dl or increase to 150 - 200 from baseline lt0.5ml/kg/hr for gt 6hr
2 Increase serum creatinine to gt 200-300 from baseline lt0.5ml/kg/hr for gt12 hrs
3 Increase serum creatinine to gt300 from baseline (or serum creatinine 4.0mg/dl with an acute rise of at least 0.5 mg/dl) lt0.3ml/kg/hr x 24 hrs or anuria x 12 hr
14AKI RIFLE Criteria
15Initial Renal US Report May 2009
- Right kidney measures 11.04 x 7.25 x 7.25 cm
- no hydronephrosis seen
- 5.92 x 4.99 x 4.3 cm hypoechoic solid-appearing
mass within the cortex of the superior pole - lesion demonstrates mildly increased flow
- also a 2.26 x 1.95 x 2.70 cm either complex cyst
with septation or two small adjacent cysts within
the inferior pole of the right kidney - Left kidney measures 11.42 x 5.06 x 5.82 cm
- exophytic 1.9 x 1.5 x 1.7 cm hypoechoic
solid-appearing mass at the superior pole of the
left kidney with vascular flow - no hydronephrosis
16Initial CT Scan Report May 2009
- 5.8 x 4.2 cm partially exophytic mixed
attenuation lesion arising from the superior pole
of the right kidney - most consistent with renal cell carcinoma until
proven otherwise. - Small exophytic lesion in upper pole of the left
kidney - 19 mm in diameter
- given its vascularity on the recent ultrasound a
solid lesion is suspected
17Renal cell carcinoma
18Renal cell carcinoma
- originate within the renal cortex
- 80 to 85 of all primary renal neoplasms
- transitional cell carcinomas
- renal pelvis are the next most common 8
- in 2009, approximately 57,800 people will be
diagnosed - 13,000 will die from RCC in the United States
- worldwide mortality exceeds 100,000 per year
- eighth most common cancer
- typically fourth to sixth decade of life
19Incidence rates are rising three times faster
than mortality rates
- Survival has improved over time
20Renal cell carcinoma
- Risk factors
- Smoking- two fold increase
- Occupational exposure
- cadmium, asbestos, and petroleum by-products
- Acquired cystic diseases of the kidney
- 30 times greater in dialysis patients with
acquired polycystic disease - malignancy typically after at least 8 -10 yrs of
dialysis - After transplant
21Renal cell carcinoma
- Risk factors
- PCKD- RCC often bilateral
- Alcohol
- Cytotoxic chemotherapy/ prior radiation
- Unopposed estrogen
- Uncontrolled hypertension
22Genetic factors Von Hippel Lindau
- Autosomal dominant
- abnormalities in chr 3pq
- increased formation of vascular tumours (mostly
benign) called hemangioblastomas and risk for
renal carcinomas and pheochromocytomas
23Reed syndrome
- Multiple cutaneous and uterine leiomyomatosis
syndrome - hereditary leiomyoma and renal cell cancer
syndrome - characterized by cutaneous leiomyomas, uterine
fibroids, and renal carcinomas - renal tumors are aggressive
- metastasize and death in patients in their 30s
24Renal Cell Carcinoma
- History
- Often zero point zero clues
- Twenty-five to thirty percent of patients are
asymptomatic - found on incidental radiologic studies
- Classic triad is not common only 10
- flank pain
- hematuria
- flank mass
- indicative of advanced disease
25Renal Cell Carcinoma
- History
- Weight loss (33)
- Fever (20)
- Hypertension (20)
- Hypercalcemia (5)
- Night sweats
- Malaise
- Varicocele
- usually left sided, due to obstruction of the
testicular vein (2 of males)
26Renal Cell Carcinoma
- Physical
- Gross hematuria
- Hypertension
- Supraclavicular adenopathy
- flank or abdominal mass with bruit
- 30 present with metastatic disease
- evaluation for metastatic disease
- lung (75)
- Varicocele and findings of paraneoplastic
syndromes raise clinical suspicion for this
diagnosis.
27Differential Diagnosis of RCC
- NHL
- Pyelonephritis
- Abscess
- Angiomyolipoma -benign
- Oncocytoma -benign
- Metastasis from distant primary
- Metastatic melanoma
- Renal adenoma benign
- Renal cyst
- Renal infarct
- Sarcoma
- Transitional cell carcinoma of renal pelvis
28Renal cell carcinoma
- challenging tumor because paraneoplastic
syndromes - hypercalcemia
- erythrocytosis
- nonmetastatic hepatic dysfunction (Stauffer
syndrome) - polyneuromyopathy
- amyloidosis
- dermatomyositis
- hypertension
29Labs to consider
- Urine analysis
- CBC count with differential
- Renal profile
- Liver function tests (AST and ALT)
- Calcium
- Erythrocyte sedimentation rate
- Prothrombin time
- Activated partial thromboplastin time
30Imaging often incidentally discovered
- CT scan
- imaging procedure of choice for diagnosis and
staging - Ultrasonography
- MRI
- PET
- mets
- Bone Scan
- Especially high alk phos
31Procedures and Subtypes of RCC
- Percutaneous cyst puncture and fluid analysis
- 5 histologic subtypes of rcc
- clear cell (75)
- chromophilic (15)
- chromophobic (5)
- oncocytoma (3)
- collecting duct (2)
- very aggressive,often younger pts
32Staging of RCC
- Robson modification of the Flocks and Kadesky
system - Stage I - Tumor confined within capsule of kidney
- Stage II - Tumor invading perinephric fat but
still contained within the Gerota fascia - Stage III - Tumor invading the renal vein or
inferior vena cava (A), or regional lymph-node
involvement (B), or both (C) - Stage IV - Tumor invading adjacent viscera
(excluding ipsilateral adrenal) or distant
metastases
33Robson staging system
34Treatment
- probability of cure is related directly to the
stage - more than 50 of patients with renal cell
carcinoma are cured in early stages
35Surgical treatment of RCC
- Surgery is curative in the majority of patients
without metastatic RCC - Preferred treatment for patients with stages I,
II, and III disease - Also used for palliation in metastatic disease
- Radical nephrectomy
- most commonly performed standard surgical
procedure today - complete removal of the Gerota fascia and its
contents, including a resection of kidney,
perirenal fat, and ipsilateral adrenal gland,
with or without ipsilateral lymph node dissection
36Surgical treatment of RCC
- Laparoscopic nephrectomy
- Advantages
- less invasive procedure, incurs less morbidity,
and is associated with shorter recovery time and
less blood loss - Disadvantages
- concerns about spillage and technical
difficulties in defining surgical margins
37Treatment of RCC
- no hormonal or chemotherapeutic regimen is
accepted as a standard of care - options are surgery, radiation therapy,
chemotherapy, hormonal therapy, immunotherapy, or
combinations of these - IL-2-T-cell growth factor and activator and
natural killer cells - Interferon alpha
- Sutent-Sunitinib
- multi-kinase inhibitor
- high response rate (40 )
- Sorafenib Nexavar
- kinase and vascular endothelial growth factor
(VEGF) multireceptor kinase inhibitor - advanced renal cell carcinoma
38Treatment
- For previously untreated patients
- low or intermediate risk
- sunitinib or the combination of bevacizumab and
interferon alpha
39Treatment Recommendations
- Radical nephrectomy
- most widely used approach
- preferred procedure when there is evidence of
invasion into the adrenal, renal vein, or
perinephric fat - Partial nephrectomy
- for smaller tumors
- particularly valuable in patients with bilateral
or multiple lesions - If renal dysfxn
- Elderly patients with significant comorbid
disease - increases the risk of surgery
- ablative techniques
- cryoablation, radiofrequency ablation
40What happened to the patient?
- Ordered records from OSU
- Cr post op was 2.5
- Did not required sx for incercerated hernia
- Reduced at bedside
- Aggressive IVF hydration
- Cr improved daily
- Peak Cr 6.1 11/16
- 5.27 3.76 3.27 3.16
41Learning Points
42Renal Cell Carcinoma Learning Points
- History
- Often zero point zero clues
- Twenty-five to thirty percent of patients are
asymptomatic - found on incidental radiologic studies
- Classic triad is not common only 10
- flank pain
- hematuria
- flank mass
- indicative of advanced disease
43Learning Points Renal Cell Carcinoma
- About 25-30 of patients have metastatic disease
at diagnosis - fewer than 5 have solitary metastasis
- surgical resection is recommended in selected
patients with metastatic renal carcinoma
44Thank You )
45- Resources
- Up to date
- http//emedicine.medscape.com/article/281340-treat
ment