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M. Riccabona
US Findings
• Same as described in all other body compartments (see respective chapters).
• Typical signs for pathological lymph nodes: large (bigger than 1cm), spherical,
conglomerated, increased number of nodes, destructed/missing hilus (Fig.14.32).
Usually found along main mesenteric vessels.
• Massive pathologic lymph nodes and suspicious congurations or bulk needs
work-up (lymphoma? granulomatous disease? specic or atypical infection—
Yersinia, Tb? etc.).
• May also have abscesses, necroses and calcications.
• For retroperitoneal nodes, mainly focus on assessment along large vessels, again
using graded compression technique.
Note In oncology patients always consider potential lymphatic drainage path-
ways—perform focused search at most crucial stations (e.g. nodes at entry of ovar­ian vein to left renal vein after left ovarian tumour).
c
d
e
Fig. 14.32 Abdominal/mesenteric lymph nodes. (a, b) Reactively enlarged inammatory mesen- teric lymph nodes (in gastroenteritis, EBV infection, etc.). (c, d) Hugely enlarged bulks of lymph nodes in abdominal lymphoma, entire extent can only be conspicuously demonstrated using pan­oramic imaging (d). (e) Bulk of enlarged, anechoic unstructured abdominal lymph nodes in a girl after renal transplantation consistent with post-transplant lymphoproliferative disease (PTLD)
14 US oftheGastrointestinal (GI) Tract
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14.2.9 Free Intraperitoneal Air
Can be seen sonographically as echogenic spots/bands with reverberation echoes, typically on highest part of abdomen, below abdominal wall, above ascites, in front of liver and outside of bowel. Can cause twinkling-like appearance on CDS (Fig.14.33).
Note If too much transducer pressure applied, air pressed away and missed! Thus,
gentle investigation at highest point of abdomen (e.g. in front of liver) advised. Depiction of free peritoneal air in constricted spaces more difcult.
Role of US
Free air can be seen, but more difcult to rule out. In suspicion actively search for it.
14.2.10 Free Intraperitoneal Fluid: Ascites
Dened as intraperitoneal uid of varying origin.
Simple (clear) or complicated (with echoes, sedimentations, septae) uid between bowel lops, or located behind bladder, in Douglas/Morrison space and around parenchymal organs (liver, spleen, kidney).
Note Site of uid does not necessarily correlate with organ of origin (e.g. in
trauma)—may be shifted by positioning, etc.
Causes: hypoproteinaemia, cardiac disease, portal hypertension, inammatory and neoplastic disease, hypervolaemia, impaired lymphatic drainage, peritoneal dial­ysis, shunt, haemorrhage (e.g. trauma, postoperative, vascular rupture and coagu­lopathy), and also with gastroenteritis/systemic infection, third space phenomena, etc.
DDx Fluid from ruptured cyst, ruptured biliary structures (bilious ascites), exuda-
tive processes (e.g. pancreatitis), localised uid versus real cyst (ovarian, mesen­teric, parenchymal organs, duplication cyst, cystic tumours, etc.), uid in constricted compartments/abscess, etc.
Fig. 14.33 Free intraperitoneal air. Echogenic lines under abdominal wall in front of the liver with reverberation artefacts, consistent with free intraperitoneal air after bowel perforation in this neonate with NEC.Note some ascites (+ +) in front of swollen kidney below liver margin (sagittal right upper quadrant section)
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M. Riccabona
Some small amount of ascites may be physiologically present (e.g. after ovula­tion), postoperatively, etc.
Note In systemic conditions, simultaneous pleural effusion commonly present—
look for it.
US Findings
• Simple ascites, anechoic uid (Fig.14.34).
• Complicated ascites, oating echoes with more or less sedimentation, brin sep-
tae and clots.
Note Functioning ventriculoperitoneal shunt will cause ascites; often at least some
parts of abdominal shunts visualised. If loculated uid collections—always check for potential obstruction to distal end of drain, within the pseudocyst collec­tion + increasing hydrocephalus (Fig.14.35).
abc
Fig. 14.34 Simple (a, b) and complex (c) intraperitoneal ascites. (a, c) Sagittal section of lower abdomen, empty bladder poorly distinguishable, the complex nature in (c) was due to haemorrhage (+ +). (b) Axial view through full urinary bladder demonstrating retrovesical free peritoneal uid
Fig. 14.35 Peritoneal shunt with cyst. Cyst (a) around abdominal end of ventriculoperitoneal shunt (b, arrow) causing shunt dysfunction/obstruction
14 US oftheGastrointestinal (GI) Tract
Fig. 14.36 Vascular problems. Huge vascular malformation of the bowel wall in the distal ileum (+ …. +, extended view US) (a) with many thrombosed veins on CDS (b). Appearance of throm­bosis on US—e.g. of iliac vessels: intraluminal thrombus nicely depictable on axial (c) and longi­tudinal section with CDS (d)
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Role of US
Very sensitive when screening entire abdomen, even for small amounts of uid. Actively search in respective compartments (e.g. in FAST). May be used to guide diagnostic puncture or drainage.
14.2.11 Mesenteric Vessels
Soma additional rare conditions such as stenosis or thrombosis exist even in child­hood. Otherwise mesenteric vessels assed for other queries such as malrotation and volvulus (see above), inammatory conditions (see above), as well as (vascular) malformations (Fig.14.36a, b).
US Findings
Visibility depends on US access—may be obscured by bowel gas.
Graded compression may help—but may obscure particularly vein (compressed and collapsed by transducer pressure).
Thrombosis appears as in other body compartments (see respective chapter) (Fig.14.36c, d).
CDS helpful for depiction and assessment of vascularisation.
Duplex Doppler essential for assessing “perfusion” (see above).
Ultrasound oftheUrogenital Tract inNeonates, Infants, andChildren
MichaelRiccabona

15.1 Requisites

15.1.1 Indications
Numerous indications—sometimes also used as screening method or for pacifying parents. Typical queries: (Foetal) pelvicalyceal distention (PCD—used in Europe) or urinary tract dilatation (UTD—used in USA), urinary tract infection (UTI), hae­maturia, failure to thrive, suspicion of VUR, obstructive uropathy, renal failure, enuresis, micturition problems, urolithiasis, involvement in systemic or syndromic disease, high blood pressure, trauma, tumour, nephritic and nephrotic syndrome, renal transplantation, pre-/postoperatively, etc.
15
15.1.2 Preparation
Good (physiologic) hydration, sufciently lled bladder.
15.1.3 Transducers
Commonly (micro-)curved arrays with age-adapted frequency:
• Additionally/alternatively linear transducers, particularly for neonates and infants,
detailed analysis of renal parenchyma, perineal access, scrotum/penis/inguinal area.
• For deep vessels and initial overview, sector transducers can be used.
M. Riccabona (*) Department of Radiology, Division of Pediatric Radiology, Medical University Graz and University Hospital Graz, Graz, Austria e-mail: michael.riccabona@medunigraz.at
© Springer Nature Switzerland AG 2020 M. Riccabona (ed.), Pediatric Ultrasound,
https://doi.org/10.1007/978-3-030-47910-7_15
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M. Riccabona
15.1.4 Positioning
Usually supine for ank and ventral access (also for perineal US), additionally prone with dorsal transducer position (paravertebral).
• Position changes also helpful for differentiating suspected sedimentations or
stones, as these move in dependent space with change of position (e.g. prone to
supine or decubitus) if intraluminal and not in papilla/xed to pelvic wall—pro-
vided sufcient distention of collecting system (Fig.15.1).
15.1.5 How toInvestigate
Always begin with bladder in longitudinal and axial sections:
• Include oblique section through ostia and distal ureters.
• Observe bladder neck.
• Bladder wall (thickness, conguration, trabeculation?), potential urachus remnants.
• Assess perivesicular space, potentially include perineal US (for urethra, best dur-
ing voiding).
• Post-void assessment (bladder/residual volume: use eq. L×W×H×correction
factor (Fig.15.2), correction factor varies based on shape of the bladder—spheric
conguration=0.5, rectangular conguration=1.0).
Assess both kidneys from ventral, lateral, and dorsal in longitudinal and cross sections:
• Evaluate entire organ; document any abnormalities in two planes.
Fig. 15.1 Dependent position of sludge oating in a somewhat dilated collecting system: US image taken in supine (a) and prone (b) position showing the gravity dependent redistribution of oating material forming a sedimentation level (arrow)—thus not xed to papilla or within distal medulla, but moving within collecting system
15 Ultrasound oftheUrogenital Tract inNeonates, Infants, andChildren
377
dard measurements for volume calculation. Correction factor varies with bladder shape. Additionally bladder wall thickness may be an indicator for bladder pathology (>2mm in full, >4mm in empty bladder), L length, W width, D depth. (b) Longitudinal (extended view technique is helpful in large-size bladders for proper measurement); (c, d) axial section—with axial measure­ments (callipers) for volume assessment; calculation depends on bladder shape that denes the correct correction factor: in spheric-ellipsoid shape factor=0.5 (c), in a rectangular shape it is 1 (d). Note additionally thickened and trabeculated bladder wall. (e, f) Open bladder neck in axial (e) and sagittal (f) view—a potential sign for bladder instability or other functional disturbance. (g) Ureteric inow jet–best seen on CDS: note the asymmetry in this example
• Assess: shape, size, position, contour, parenchymal echogenicity, and cortico-
medullary differentiation, collecting system dilatation (if enlarged, measured in
axial plane) and thickening of pelvic wall and peripelvic fat/brotic tissue.
• Calculate renal volume (L×W×H×0.53).
• Assess vascular anatomy (CDS) (e.g. accessory renal artery); follow vessels to ori-
gin or drainage (e.g. retro-aortal left renal vein). Add spectral analysis if indicated
from main as well as intrarenal vessels (from upper, middle, and lower segment).
• aCDS is applied for peripheral vasculature (e.g. focal perfusion defects?).
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M. Riccabona
Note Physiologic difference in colour intensity between highly vascularised cortex
and less vascularised medullae. Compare both sides in relation to perirenal structures.
• Always assess perirenal space (adrenal gland).
• Try to assess pelvi-ureteric junction (open? obstructed by vessel? kinking?…);
follow ureter downwards, if dilated.
• Assess collecting system after voiding (changes in dilatation?).
• Consider CEUS for lesion characterisation (e.g. complicated cyst) or equivocal
ndings on baseline US/(a)CDS (e.g. suspected perfusion defects, traumatic
lesions …).
CDS Document ureteric jet into bladder (symmetric? position of ostium?), vascu-
lar anatomy extrarenally as well as main intrarenal arteries (proper scale setting not to miss aliasing and turbulences at sites of possible stenosis or AVF…). Assess for possible twinkling (calcications and sedimentations) (Fig.15.2f),
• New sensitive (a)CDS techniques (such as SMI) even better depict jets and
“swirls”.
15.1.5.1 Diuretic US
Used for assessment in dilated urinary tracts/distended pelvicalyceal system: stan­dardised diuretic stress induced by medication (e.g. furosemide, dose=1mg/kg, up to 20mg) given orally or IV (acts faster). Repeat assessment of kidney till ndings (dilatation of collecting system, Doppler ow spectra) have returned to baseline— delayed or missing normalisation of ow patterns after diuretic stress indicates sig­nicant obstruction.
15.1.6 Contrast-Enhanced Voiding Urosonography (ce-VUS)
Denition
ce-VUS=sonographic test for vesico-ureteric reux (VUR).
Has become a standard procedure for VUR evaluation since UCA approved for paediatric use. Is reliable, no radiation, can be performed at bedside (see also chap­ter on contrast-enhanced ultrasound). Short description outlined here, too.
How To Do After assuring sterile urine and initial US assessment performed, ure­thral catheter placed (or suprapubic puncture) and bladder emptied:
• Then bladder gradually lled by drip infusion (infusion height <40cm above
bladder level—physiologic lling pressure):
– Potential antibiotics added (or antibiotic prophylaxis).
15 Ultrasound oftheUrogenital Tract inNeonates, Infants, andChildren
379
• Alternating scanning of retrovesical space+bladder as well as both kidneys dur-
ing lling:
– Drip infusion may be used as manometer to see moments of increased bladder
pressure during lling—may indicate unstable bladder, helps to depict moments of high pressure VUR.
• Fractional instillation of UCA (at present mostly Sonovue®/Lumason®, Bracco/
Italy), concentration = 0.1–1.0 (3.0%)% of actual bladder lling volume,
depending on transducer and equipment (Fig.15.3).
– Company recommendation (Lumason/SonoVue) 1mL/lling. – Alternatively mix solution of saline with 0.1–1.0% UCA in plastic container,
and use this for drip infusion as specied above.
• Ongoing alternating assessment of bladder, retrovesical space/distal ureter, and
both kidneys.
Note: In rst years of life, cyclic lling (three cycles) recommended.
• Scanning continued when bladder is lled (urge or spontaneous voiding).
• Assess urethra by perineal US (during voiding, possibly use dedicated cycle/last
cycle with catheter removal):
• After voiding, check kidneys for potential reuxed UCA within collecting sys-
tem, CM drainage dynamics, and bladder for residual urine/diverticulae.
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Fig. 15.3 ce-VUS: bladder and ureter. (a) Filling of the bladder with saline drip infusion (30–40 cm H instilled—bladder lumen gets distended with echogenic material. Note the echoic CM-lled distal right ureter behind the bladder, only clearly detectable by the contrast image. (c) Single contrast image: echogenic contrast in a megaureter in dilating VUR (V°). (d) Single contrast image: con­trast reux into narrow distal ureter, with gapping and pathologically shaped UVJ. (e) Voiding on ce-VUS (transvesical sagittal access in an infant): only proximal urethra (++) seen from abdomi­nal sagittal approach/view
0 pressure) via catheter. (b) Dual image technique (left—contrast image): UCA
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Fig. 15.4 Male urethra during voiding on ce-VUS. (a) Neonatal male urethra during voiding, perineal access: voiding attempt before catheterisation, no UCA; only the urine works as physio­logic CM—outlining the proximal urethra to the level of the pelvic oor. (b, c) Two images of male neonatal urethra during voiding on ce-VUS; note the dynamic changes of the shape of the proximal urethra and the better visualisation using the coloured contrast image—particularly helpful if the room cannot be properly darkened such as in bedside examinations (e.g. in NICU)
M. Riccabona
• At last cycle, catheter withdrawn for proper view of unobstructed urethra on
perineal US (Fig.15.4)—unless same catheter used for complementing focused
uoroscopic VCUG.
– Consider stepwise catheter withdrawl with still running UCA-infusion, to
gradually assess urethra—not to miss, e.g. ectopically inserting reuxing ure­ters or more subtle urethral pathology.
Note Urethra only assessable if viewed during voiding.
Tip If VCUG is planned always perform ce-VUS rst (ionidated CM is heavier
and thus may obscure VUR on ce-VUS if done after conventional VCUG).

15.2 Normal Findings

15.2.1 Bladder
Well-lled bladder has smooth contour and muscular wall, not >2–4 mm thick (depends less on age than on lling):
• Ostium at latero-cranial end of bladder trigone as well as distal ureters often seen
physiologically in well-lled bladder and good-hydrated children.
• Assess bladder volume (see above and respective chapter). Simple equation
often used to dene normal range: volume (mL)=[age (in years)+2]×30.
• Bladder neck closed unless there is an urge to void; after voiding bladder neck
should be closed. Open bladder neck, thickened bladder wall, irregular inner
contour with trabeculation and pseudo-diverticulae, high bladder tension, or
atypical contour may raise suspicion of neurogenic bladder/functional
disturbance.