Study Case An
8-month-old Rottweiler with Renal Failure
Claire M. Surber,
DVM; Heather Tarpley, DVM, Kenneth S. Latimer, DVM, PhD, Bruce E. LeRoy,
DVM, PhD, Cathy Brown, DVM, PhD
Class of 2005 (Surber),
Department of Pathology (Tarpley, Latimer, LeRoy), Diagnostic Laboratory
(Brown), College of Veterinary Medicine, University of Georgia, Athens,
GA 30602-7388

Signalment
- Canine, Rottweiler, F/S, 8-month old
Presenting
problems (04/22/04) Renal failure (with azotemia
and isosthenuria, as diagnosed by the referring veterinarian), intermittent
vomiting and diarrhea, weight loss, lethargy, polyuria and polydipsia
Medical
history Renal failure (azotemia and isosthenuria),
a gastrotomy was performed on 03/02/04 to remove a foreign body.
Laboratory
Data -
| Complete
Blood Cell Count - |
| |
04/22/04 |
Units |
Reference
Interval |
| Hct |
32.9
L |
% |
35.0-57.0 |
| RBC |
4.23
L |
x
106/µl |
4.95-7.87 |
| Hgb |
11.0
L |
g/dl |
11.9-18.9 |
| MCV |
77.9
H |
fl |
66-77 |
| MCH |
26.1 |
pg |
21.0-26.2 |
| MCHC |
33.5 |
g/dl |
32.0-36.3 |
| Platelets |
321 |
x
103/µl |
211-621 |
| MPV |
8.5 |
fl |
6.1-10.1 |
| Plt
estimate |
Adequate,
few shift platelets |
|
|
| nRBC |
0,
slight anisocytosis |
/100WBC |
|
| WBC
morphology |
Occasional
reactive lymphocyte |
|
|
| WBC |
9.4 |
x
103/µl |
5.1-13.0 |
| Seg |
7.050
(75%) |
x
103/µl |
2.9-12.0 |
| Band |
0.00
(0%) |
x
103/µl |
0.0-0.45 |
| Lymph |
1.786
(19%) |
x
103/µl |
0.4-2.9 |
| Mono |
0.282
(3%) |
x
103/µl |
0.1-1.4 |
| Eos |
0.282
(3%) |
x
103/µl |
0.0-1.3 |
| Baso |
0.000
(0%) |
x
103/µl |
0.0-0.14 |
| Biochemical
Profile - |
| |
04/29/04 |
04/28/04 |
04/26/04 |
04/24/04 |
04/23/04 |
04/22/04 |
Units |
Reference Interval |
| Total
protein |
N/A |
N/A |
5.0
L |
4.3
L |
N/A |
5.0
L |
g/dl |
5.2-7.3 |
| BUN |
54
H |
64
H |
52
H |
50
H |
64
H |
71
H |
mg/dl |
10.0-30.0 |
| Creatinine |
3.5
H |
4.3
H |
3.2
H |
2.9
H |
3.4
H |
3.5
H |
mg/dl |
0.5-1.5 |
| Albumin |
N/A |
N/A |
2.9 |
2.6 |
N/A |
3.0 |
g/dl |
5.2-7.3 |
| Alk
Phos |
N/A |
N/A |
N/A |
117 |
N/A |
142
H |
U/L |
13-122 |
| ALT |
N/A |
N/A |
N/A |
25 |
N/A |
37 |
U/L |
12-108 |
| Glucose |
N/A |
N/A |
N/A |
112 |
N/A |
98 |
mg/dl |
77-120 |
| Sodium |
143
L |
148 |
148 |
149 |
153 |
152 |
mmol/L |
146-154 |
| Potassium |
5.9
H |
6.2
H |
5.5
H |
4.5 |
4.6 |
5.2
H |
mmol/L |
3.9-5.0 |
| Chloride |
107 |
111 |
113 |
114 |
118 |
119 |
mmol/L |
107-125 |
| Bicarbonate |
18 |
16 |
15 |
16 |
13
L |
11
L |
mmol/L |
14-24 |
| Anion
Gap |
24 |
27 |
26 |
24 |
27 |
27 |
mmol/L |
11-28 |
| Calcium |
10.9 |
10.8 |
10.8 |
9.7 |
10.2 |
10.8 |
mg/dl |
9.3-11.4 |
| Phosphorus |
12.3
H |
13.6
H |
12.4
H |
13.2
H |
13.8
H |
15.9
H |
mg/dl |
3.2-5.4 |
| Magnesium |
N/A |
N/A |
N/A |
2.1 |
N/A |
2.5
H |
mg/dl |
1.6-2.4 |
| Cholesterol |
N/A |
N/A |
N/A |
291
H |
N/A |
364
H |
mg/dl |
129-264 |
| Total
Bilirubin |
N/A |
N/A |
N/A |
0.1 |
N/A |
0.1 |
mg/dl |
0.0-0.2 |
| Hemostasis
Profile - |
| Test |
04/26/04 |
Units |
Ref. Range |
| PT |
5.2 L |
Sec. |
5.8-9.8 |
| APTT |
10.9 |
Sec. |
9.4-15.1 |
| TT |
9.9 |
Sec. |
3.7-10.0 |
| Urinalysis
- |
| |
04/24/04 |
04/22/04 |
| Urine
source |
Cystocentesis |
Cystocentesis |
| Color |
Yellow |
Yellow |
| Turbidity |
Clear |
Hazy |
| Specific
gravity |
1.010 |
1.012 |
| pH |
6.5 |
5.0 |
| Protein |
2+ |
2+ |
| Glucose |
Negative |
Negative |
| Ketones |
Negative |
Negative |
| Bilirubin |
Negative |
Negative |
| Blood |
Moderate |
Small |
| Sediment
- |
RBC |
<10
/ hpf |
<10
/ hpf |
WBC |
5-10
/ hpf |
<5
/ hpf |
Casts |
N/A |
1-3
Coarse Granular / hpf |
Epithelium |
Few
Round / hpf |
Few
Squamous / hpf |
Crystals |
Few
Amorphous |
Few
Amorphous |
Miscellaneous |
Few
Fat |
Few
Fat |
| Urine
Chemistry - |
| |
04/24/04 |
04/23/04 |
Units |
Ref. Range |
| Protein (urine) |
222.6 |
256.1 |
mg/dl |
NRR |
| Creatinine (urine) |
25.2 |
47.4 |
mg/dl |
NRR |
| Urine Protein:Creat
ratio |
8.83 |
5.40 H |
ratio |
0.0-0.3 |
Additional
Diagnostic Tests
- Antinuclear
Antibody Test: Negative
- Rocky
Mountain Spotted Fever, Ehrlichia, and Lyme Disease Titers: Negativ
- Leptospirosis
Titer: Negative
- Abdominal
Radiographs (04/22/04): The right kidney is poorly visualized; no intra-abdominal
abnormalities are identified.
- Abdominal
Ultrasound (04/22/04): Both kidneys were hyperechoic (isoechoic to the spleen),
but were within normal limits with respect to size and shape. The
right renal pelvis was slightly dilated. No abnormalities were noted
within the liver, spleen, urinary bladder, or adrenal glands.
Problems -
1. Renal
Failure, characterized by Azotemia and Isosthenuria. The
combination of elevated blood urea nitrogen (BUN) and creatinine
concentrations with isosthenuric urine indicates the presence of
renal failure. BUN is normally equal to the serum urea nitrogen
because of equilibration within the total body water compartment,
and the kidney is the most important route of urea excretion. Urea
is passively filtered through the kidneys, and an increased BUN
indicates a decreased glomerular filtration rate (GFR). Creatinine
is freely filtered by the glomerulus, and tubular resorption does
not occur. An increased creatinine concentration with an elevated
BUN is termed azotemia, and can be due to pre-renal, renal, and
post-renal causes. When azotemia occurs with isosthenuric urine,
especially in the face of dehydration, this indicates renal azotemia
is an indication of renal failure.
Renal azotemia
occurs when at least ¾ of the nephrons are nonfunctional. The GFR
becomes significantly decreased, and the animal is not able to concentrate
urine, even in the face of dehydration. Renal azotemia can be either
acute or chronic; causes of acute renal failure include infectious
agents such as leptospirosis, Rocky Mountain Spotted Fever, and ehrlichiosis;
prolonged anesthesia/hypoperfusion, and nephrotoxins (non-steroidal
anti-inflammatory agents, aminoglycosides, sulfonamides, ethylene
glycol, heavy metals, and grape/raisin toxicity). Other diseases
such as glomerulonephritis, arteritis, and pancreatitis may cause
acute renal failure. Chronic renal failure may be due to congenital
defects, such as ectopic ureters that may lead to a pyeolonephritis,
nephrotoxins, glomerulonephritis, amyloidosis, other congenital defects,
polycystic kidney disease, and diabetes mellitus.
Regarding this
patient, the ultrasound finding of hyperechogenicity of the kidneys
may occur in animals with both acute and chronic renal failure. However,
the normal size and shape of the kidneys support more of an acute
problem. Conversely, the presence of clinical signs for 1 ½-months
suggests a more chronic cause of renal failure. A kidney biopsy was
performed to identify the etiology of the renal failure, to distinguish
between acute and chronic renal failure, and to discern reversible
versus nonreversible damage to the kidneys.
2. History
of Gastrotomy for Foreign Body Removal. A
gastrotomy was performed under general anesthesia on 3/2/04 to
remove a foreign body. This patient did not have evidence of renal
disease pre-operatively. It is possible that this anesthetic episode
exacerbated subclinical renal disease. General anesthesia causes
decreased renal perfusion, which when coupled with a subclinical
renal pathology, could result in clinical renal failure.
Additionally, this
surgical procedure may be responsible for the inappetence, vomiting,
and diarrhea experienced by this patient. A stricture could have
formed at the surgical site, resulting in obstruction of pyloric
outflow obstruction and possible esophagitis. A reflux esophagitis
could have also occurred under anesthesia, resulting in such clinical
signs. However, the vomiting and diarrhea could also be solely due
to the presence of uremia and renal failure. Diagnostics such as
a barium study, esophagram, or endoscopy could help to rule out gastrointestinal
causes of the vomiting and diarrhea. A negative fecal examination
eliminated parasitic causes.
3. Anemia. Anemia
is present due to a low hematocrit of 32.9, a low RBC of 4.23, and
a low Hgb of 11. The anemia is classified as mildly macrocytic (due
to increased MCV) and normochromic (due to normal MCHC). In this
case, the anemia is most likely due to the renal failure (decreased
renal production of erythropoietin) and possibly loss of blood through
the intestinal tract. The dog had a history of black tarry stool/melena,
indicating the presence of digested blood in the feces. Additional
rule-outs include a mild anemia that is commonly present in puppies,
and anemia of chronic disease.
4. Hypoproteinemia,
Proteinuria, and Elevated Urine Protein:Urine Creatinine Ratio. Hypoproteinemia
may be either relative (due to dilution of plasma proteins by excess
fluids), or absolute (due to loss of albumin and globulins). An
absolute hypoproteinemia is most likely in this dog, because the
2+ proteinuria and an isosthenuric urine specific gravity, suggests
a marked loss of protein in the urine. Decreased glomerular function
allows small proteins to be lost through the glomerulus into the
urine. A urine protein:urine creatinine (UP:UC) ratio was performed
to better characterize the urinary protein loss. A UP:UC < 0.5
is within reference limits. A ratio between 0.5-1.0 is questionable.
However, a UP:UC > 1.0 indicates a true renal proteinuria, and
may be due to hemorrhage (presence of occult blood in urine, >5
RBCs/hpf, and the presence of trauma, inflammation, or neoplasia),
inflammation (>5 WBC/hpf, bacteruria), or renal disease (absence
of occult blood in urine, significant cellular sediment, +/- casts).
This dog had an
initial UP:UC of 5.4, which subsequently increased to 8.83. A UP:UC
ratio > 1.0 and < 3.0 indicates a primary tubular disease,
where the major proteins lost are low molecular weight globulins.
A UP:UC > 3.0, and often greater than 5.0, indicates primary glomerular
disease, which was most likely in this dog. With primary glomerular
disease, the major protein lost is albumin, due to either glomerulonephritis
(UP:UC 5-15) or amyloidosis (UP:UC > 18). It is possible to have
both glomerular and tubular disease present simultaneously, as this
patient had hypoalbuminemia and an A:G ratio within reference limits.
5. Hyperkalemia. An
elevated potassium level may be due to either increased dietary intake
or, as most likely in this case, decreased urinary excretion of potassium.
With the presence of renal failure and a decreased GFR, this patient
had a decreased ability to filter potassium through the glomerulus
and into the urine.
6. Decreased
bicarbonate concentration. A
decreased bicarbonate concentration with a normal anion gap is
most likely due to bicarbonate loss through the kidneys as well
as with the diarrhea. A fractional excretion of bicarbonate could
be performed to quantify bicarbonate lost in the urine.
7. Hyperphosphatemia. Hyperphosphatemia
can be caused by increased dietary intake, a shift in phosphorus
from the intracellular to extracellular compartment, or decreased
excretion in the urine. The most common cause, as demonstrated by
this case, is renal failure. Other causes of hyperphosphatemia include
to consider are Vitamin D toxicosis and hypoparathyroidism. This
patient was treated with aluminum hydroxide to bind the excess phosphorus
and aid in its excretion.
8. Hypermagnesemia. Hypermagnesemia
may be caused by either increased dietary intake or decreased renal
excretion. The mildly increased magnesium concentration in this patient
was likely due to its renal failure.
9. Hypercholesterolemia. A
hypercholesterolemia can be due to the post-prandial increase in
serum cholesterol, a high fat and cholesterol diet, diabetes mellitus,
hypothyroidism, hyperadrenocorticism, and protein-losing disorders
such as renal disease. In this dog, the hypercholesterolemia (along
with azotemia, hypoalbuminemia, and proteinuria), is most likely
due to the nephrotic syndrome. While the pathophysiologic mechanism
is still poorly understood, it is believed to be caused by an increase
in hepatic synthesis of cholesterol and a reduction in lipoprotein
catabolism in plasma.
10. Decreased
PT. Prior
to the kidney biopsy, a hemostasis profile was performed to evaluate
clotting ability. The prothrombin time (PT) was mildly decreased,
at 5.2 seconds, with a reference range of 5.8-9.8 seconds. Both
the APTT and TT were within the normal reference range. A decreased
prothrombin time suggests a hypercoagulable condition, which in
animals with severe proteinuric renal disease may be due to loss
of anticoagulant molecules such as antithrombin III in the urine.
11. Presence
of Coarse Granular Casts in the Urine. Casts
are composed of Tamm-Horsfall protein that is produced by the distal
tubular epithelial cells. They are formed when the urine is more
acidic. Granular casts are the most common type of casts observed
and are composed of mucoprotein, plasma proteins, degenerate cells,
and tubular debris. The presence of casts indicates tubular change,
and while small numbers may occasionally be present in healthy
individuals, they likely indicate significant tubular disease in
this patient.
 |
| Photomicrograph of a granular cast |
Laparoscopic-Assisted
Kidney Biopsy of the Left Kidney — A
laparoscopic-assisted kidney biopsy was performed on 04/27/04, in
which two 14-gauge Tru-cut biopsies were taken of the left kidney
and submitted for histopathologic evaluation.
Histopathologic Evaluation:
Renal biopsy samples revealed that, within the cortex, the Bowmans
capsules were significantly dilated and slightly increased in thickness.
Glomerular tufts were atrophic with mildly increased cellularity (mesangial
cell hyperplasia), and there was a slight thickening of the capillary
basement membrane. Immune-complex deposits were not revealed with special
stains.
Diagnosis: Membranoproliferative
Glomerulopathy with glomerulocystic change
Prognosis: Guarded
to Poor
 |
| Kidney
biopsies demonstrate abnormal glomeruli containing shrunken, atrophic
glomerular tufts and marked dilation of Bowmans capsule. |
Summary — The
significant glomerular changes found, such as cystic dilation of Bowmans
capsule and the atrophic glomerular tufts, are consistent with a "juvenile
nephropathy," which is suspected of being familial. Familial and
juvenile nephropathies are documented in many dog breeds, with the
onset of renal failure occurring from a few weeks of age to several
years, but in most cases between 4-18 months of age. Such congenital
nephropathies, often characterized by membranoproliferative glomerulonephritis
with glomerulocystic changes, have been documented in Doberman Pinschers,
and similar lesions have been reported in four related Rottweiler pups.
The glomerular changes in this dog may be due to ultrastructural abnormalities
in basement membrane collagen, as suggested the discovery of similar
lesions in two Rottweiler puppies (personal communication, Dr. Cathy
Brown, Athens Diagnostic Laboratory, College of Veterinary Medicine,
University of Georgia).
References
1. Cook SM, Dean
DF, Golden DL, Wilkinson JE, Means TL. Renal failure attributable to
atrophic glomerulopathy in four related Rottweilers. J Am Vet Med
Assoc 202(1):107-109, 1993.
2. Latimer KS, Mahaffey
EA, Prasse KW (eds): Duncan & Prasses Veterinary Laboratory
Medicine: Clinical Pathology, 4th ed. Ames, Iowa State Press, 2003.
3. Photos of granular
casts from: http://www.agora.crosemont.qc.ca/urinesediments/doceng/doc_003.htm
4. MacWilliams P.
Profiling the Urinary System II. Western Veterinary Conference 2003,
School of Veterinary Medicine, University of Wisconsin-Madison, Madison,
WI, USA (http://www.vin.com/)
Acknowledgment
"Gardening Buddies" by
Marie Girio Brummett is from the Maple
Springs dog, wildlife, nature art print gallery and is used with
permission. |