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Abdominal Ultrasonographyin Small Animals
Abdominal Ultrasonographyin Small Animals
ABSTRACT
This paper completes a two part review of
abdominal ultrasonography in small animals.
Indications, examination technique and inter-
pretation of abnormal findings are described and
illustrated using clinical cases.
295
C. R. LAMB
THE KIDNEYS
~
296
Abdominal ultrusonogruphy in srnall animals
sinus usually contains an echogenic fat pad. A change in tissue echogenicity relies on compar-
detailed appreciation of the internal anatomy of ison with an adjacent organ which may be
the kidney necessitates use of a high frequency assumed to be normal. For example, the liver
transducer, as fine structural detail will not be normally has a coarse, hypoechoic echotexture
visualised if too low a frequency transducer is compared to the spleen. The right kidney may be
used, or if care is not taken to obtain true dorsal, conveniently compared with the adjacent caud-
sagittal or transverse imaging planes (Fig 6). Sim- ate lobe of the liver. It has been assumed that the
ilarly, precise ultrasonographic measurement of echogenicity of the renal cortex in dogs and cats
kidney length requires an accurate sagittal sec- is normally equal to or less than that of the adja-
tion. In the dog and cat an appropriate sagittal cent liver (Konde and others 1984, Feeney and
orientation is indicated by visualisation of paral- others 1985b), as is the case in most humans
lel echogenic bars representing the paired renal (Rosenfield and Siegel 1981). However, a recent
diverticula (Walter and others 1987a). Ultrasono- study has demonstrated that the renal cortex in
graphic measurements tend to slightly underesti- normal humans may be hypoechoic, isoechoic, or
mate true kidney length because at the poles of hyperechoic compared to the adjacent liver (Platt
the kidney the capsule is oriented roughly paral- and others 1988). Hartzband and others (1989)
lel to the ultrasound beam when the kidney is have made similar observations in dogs. They
imaged from its lateral aspect. This prevents pro- performed ultrasound examinations of the right
duction of a specular echo from the capsule kidney and liver in 34 young healthy bitches and
which therefore is not clearly visualised. More found that at 5 MHz 33/34 dogs had a hypo- or
accurate kidney length determinations may be isoechoic renal cortex compared to the liver; one
made if the kidneys are imaged from their caudal dog had a hyperechoic renal cortex. When
poles. Normal kidney length in the cat is 3.8 to imaged at 7.5 MHz 26/34 renal cortices were
4.4 cm with a cortical thickness of 2 to 5 mm more echogenic than at 5 MHz, and 14/34 were
(Schummer and others 1979). In the dog kidney hyperechoic compared to the liver. Wedge and
length is variable depending on breed; cortical core biopsies obtained two days later confirmed
thickness is normally 3 to 8 mm (Schummer and that the tissues were normal. Hence, although
others 1979). In dogs undergoing diuresis, the there does appear to be a relationship between
medulla may increase in size (Konde 1985); this renal echogenicity and certain kidney diseases
effect is less apparent in the normal cat (Walter (Rosenfield and Siegel 1981, Hricak and others
and others 1987a, c). 1982, Feeney and others 1985b), comparing the
Renal abnormalities identified by ultrasono- echogenicity of the kidney cortex to that of the
graphy may be subdivided into diffuse alter- liver is not a reliable method of diagnosing renal
ations in tissue echogenicity or architecture and disease. Furthermore, the transducer frequency
focal abnormalities. As previously described must be known when interpreting the results of
with respect to the liver, recognition of a diffuse renal ultrasonography.
FIG 6. Ultrasound images of a normal canine kidney in a water bath. (a) Dorsal plane image showing clear corticomedullary dis-
tinction, radiating diverticula and echogenic fat in the renal sinus (s). (b) Sagittal plane image showing the parallel bars of the
renal diverticula (arrows). This is an appropriate orientation for measurement of kidney length. (c) Transverse plane image show-
ing the diverticula branching around the renal crest (r)
297
C. K. L A M E
298
Abdominal ultrasonography in S J I I U ~onjmals
~
the kidney parenchyma is compressed into a thin slightly easier to image than the right because
layer around the urine containing pelvis, produc- searching for the right adrenal usually requires
ing an appearance which could be confused with an intercostal approach with ribs and respiratory
a large renal cyst on ultrasonography (Fig 11). motion causing difficulties. Hence, although
Descriptions of ultrasonographic findings in adrenal ultrasonography may be requested in ani-
pyelonephritis are conspicuously absent from the mals with signs of hyperadrenocorticism or
veterinary literature, probably reflecting a low phaeochromocytoma, inability to visualise the
sensitivity of ultrasonography for this condition gland (particularly the right gland) does not rule
similar to that described in humans (Traisman out the possibility of mild enlargement. Similar-
and others 1986, Sty and others 1987). Cortical ly, the ultrasonographic finding of a unilateral
scintigraphy is a more sensitive and specific adrenal mass does not rule out the possibility of
screening test for renal infection. bilateral adrenal enlargement, for example due
to pituitary-dependent hyperadrenocorticism
(Kantrowitz and others 1986). Finally, it must be
THE ADRENAL GLANDS ~ ~~ ~ remembered that hyperadrenocorticism in dogs
is not always associated with measurable adrenal
The ultrasonographic appearance and anatomi- gland enlargement (Kelly and others 1971). For
cal landmarks of normal canine adrenal glands these reasons ultrasonography is not an ideal
have recently been described (Voorhout 1988). technique for the investigation of adrenal gland
Identification of the normal adrenal requires disease although it is more sensitive than
careful examination of the retroperitoneum survey radiography and, unlike tomography or
medial or just cranial to the cranial poles of the computed tomography, does not require general
kidneys. The left adrenal lies slightly caudal, and anaesthesia.
the right cranial, to the origin of the cranial Adrenal masses produce a variety of ultrasono-
mesenteric artery. Again, a high frequency trans- graphic appearances, being described as hypo-
ducer provides the best resolution of the adrenal echoic (Fig 13), hyperechoic or heterogeneous,
glands, which are usually less than 3 cm long sometimes with echogenic foci due to calcifica-
and flattened dorsoventrally. The adrenal me- tion (Kantrowitz and others 1986, Poffenbarger
dulla is hyperechoic compared to the cortex. A and others 1988, Voorhout 1988). Adrenal haem-
normal canine adrenal gland is shown in Fig 1 2 . orrhage may also produce a variety of appear-
The ultrasonographic appearance of normal ances depending on the duration of the lesion
feline adrenals has not been established. (Wu 1989). Fig 14 shows invasion of the caudal
In dogs, the left adrenal gland appears to be
299
C. R. LAMB
300
Abdominal ultrasonography in small animals
THE PROSTATE
Indications for prostatic ultrasonography FIG 19. Longitudinal ultrasound image of the prostate of a
include prostatomegaly, signs of urinary tract castrated dog without clinical signs of prostatic disease. The
infection, haematuria, haemospermia and caudal gland is smaller than in the intact male (approximately 2.4
cm in this case) and is uniformly hypoechoic compared to the
abdominal pain, As described for the ovary and surrounding pelvic tissues
uterus, satisfactory ultrasonographic examination
of the prostate requires a high frequency trans- The canine prostate is usually examined by
ducer. In man, rectal ultrasound probes provide applying a sector transducer cranial to the pubis
the best images of the prostate (Lee and others and directing the beam caudally. In large dogs, a
1987). Use of rectal ultrasound transducers has
linear-array probe designed for large animal use
been described for examination of the canine may be inserted into the rectum. Using the blad-
prostate (Miyashita and others 1984); however, der as an anatomical landmark, the prostate may
the high cost of rectal probes specifically for be identified just caudal to the bladder neck,
prostatic imaging has inhibited their use by encircling the urethra. The flimsy prostatic cap-
veterinary ultrasonographers. sule of the dog is not well seen, making it diffi-
cult to define the exact borders of the gland on
ultrasonography unless it has a distinctly differ-
ent echotexture to the surrounding pelvic tissues.
The normal prostate is a symmetrical structure of
uniform echotexture except in cases where a
periurethral or hilar echogenic zone is apparent.
Benign prostatic hypertrophy, which occurs in
50 per cent of dogs over four years and approxi-
mately 90 per cent over five years (Berry and oth-
ers 1986), may produce a diffuse, mild increase
in echogenicity (Fig 18). In the castrated male the
prostate is small and hypoechoic (Fig 19).
Previous reviews of canine prostatic ultra-
FIG 17. Ultrasound image of a large, complex mass adjacent
sonography described changes common to a
to the urinary bladder. Ovarian cystadenoma was removed at variety of prostatic diseases (Feeney and
laparotoiny others 1985a, 1987). For example, prostatic
301
C. K. LAMB
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302
Abdominal ultrasonography in small animals
303
C. R. LAMB
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