Kidneys and adrenal glands
Kidneys, ureters and adrenal glands on imaging: anatomy, variants and masses
Kidney, ureter and adrenal anatomy for FCPS Part 1 imaging: relations, hilum, segmental arteries, ureteric narrowings, variants and adrenal masses. Each fact is linked to what it explains on ultrasound, CT, urography and nuclear scans.
One of the most tested topics in past papers
Position and fascia
- Kidneys lie from about T12 to L3; the hilum is at L1 (transpyloric plane); the right kidney sits lower because of the liver. Adult length 10–12 cm.
- They lie on the sloping psoas, so the lower poles are more lateral than the upper poles and the hilum faces anteromedially. They move down 2–3 cm on deep inspiration.
- Renal (Gerota) fascia encloses kidney, adrenal and perirenal fat. It is closed above and laterally but open inferiorly, so perinephric pus or blood tracks down towards the iliac fossa and pelvis.
- Renal angle: below the 12th rib, lateral to erector spinae.
Relations
| Surface | Right kidney | Left kidney |
|---|---|---|
| Anterior | Adrenal, liver (Morison pouch between), D2 in front of the hilum, hepatic flexure | Adrenal, spleen, stomach, pancreas body and tail (direct contact), splenic vessels, splenic flexure, jejunum |
| Posterior (both) | Diaphragm, 12th rib, psoas, quadratus lumborum, transversus; subcostal, iliohypogastric and ilioinguinal nerves | Same, with the 11th and 12th ribs |
- The abdominal aorta lies to the left of the IVC on the vertebral bodies and divides at L4. An aortic aneurysm is commonest below the renal arteries (infrarenal); rupture gives a pulsatile, expansile mass above the umbilicus with back pain and shock, and the blood collects in the left retroperitoneum.
Hilum, vessels and internal structure
- Order at the hilum from front to back: vein, artery, pelvis.
- Right renal artery passes behind the IVC; left renal vein passes in front of the aorta, below the superior mesenteric artery, and receives the left gonadal and left adrenal veins.
- The renal artery divides into segmental arteries, which are end arteries, so blocking one gives a pale wedge infarct. Branches run interlobar (in the renal columns), then arcuate (arching over the bases of the pyramids at the corticomedullary junction), then interlobular (radially into the cortex) to the afferent arterioles.
- A relatively avascular plane lies just behind the lateral convex border between anterior and posterior segmental territories; percutaneous nephrostomy enters a posterior lower-pole calyx for this reason.
- Accessory renal arteries persist from the series of arteries used during ascent; one crossing the pelviureteric junction can cause PUJ obstruction (loin pain after a fluid load, dilated pelvis, normal ureter).
| Structure | Direction and content |
|---|---|
| Renal column (of Bertin) | Cortex dipping down between pyramids into the medulla; carries interlobar vessels |
| Medullary ray | Straight tubules and collecting ducts running up from the medulla into the cortex between convoluted tubules; centre of a lobule |
| Pyramid and papilla | Loops of Henle, vasa recta and collecting ducts converging on the papilla, cupped by a minor calyx |
- The parts of the nephron most sensitive to ischaemia are the straight (S3) part of the proximal tubule and the thick ascending limb in the outer medulla: high oxygen demand in a region of low oxygen tension. This is acute tubular necrosis.
Normal imaging appearances and their physiology
- Ultrasound (adult): cortex less echogenic than liver, pyramids darker, sinus fat bright. Neonate: cortex as bright as liver with prominent dark pyramids is normal.
- Hypertrophied column of Bertin: cortex-like tissue projecting into the sinus with the same echogenicity as cortex (a pseudotumour). Fetal lobulation: smooth notches between pyramids; scars lie over calyces.
- CT phases: corticomedullary at 30–40 s (cortex receives most renal blood flow), nephrographic at about 100 s (uniform), excretory after several minutes.
- Obstructed kidney: the nephrogram appears late and grows progressively denser for hours. Tubular flow is slow, so more water is reabsorbed and the filtered contrast becomes concentrated in the tubules. Rupture of a calyceal fornix gives a separate sign, contrast leaking into the perirenal space.
- Rim sign: infarct with a preserved subcapsular rim supplied by capsular collaterals. Reverse rim: cortical necrosis (abruption with DIC): cortex dark, medulla and thin subcapsular rim enhancing.
- Page kidney: a subcapsular haematoma compresses the kidney, which becomes ischaemic and releases renin, causing hypertension. A perirenal haematoma outside the tough capsule rarely compresses enough to do this.
| Nuclear tracer | Handling | Use |
|---|---|---|
| Tc-99m DTPA | Filtered only | GFR, split function |
| Tc-99m MAG3 | Mostly tubular secretion | Obstruction; with captopril for renal artery stenosis |
| Tc-99m DMSA | Bound in proximal tubule cells | Cortical scars, which favour the poles (compound papillae allow intrarenal reflux) |
| MIBG | Taken up by the noradrenaline transporter | Phaeochromocytoma, neuroblastoma |
- Captopril renography: in a stenotic kidney, GFR is held up by angiotensin II constricting the efferent arteriole. An ACE inhibitor removes efferent tone, glomerular pressure falls and uptake and excretion on that side become delayed. The same mechanism causes acute kidney injury when ACE inhibitors are given in bilateral stenosis.
Development and variants
- Ureteric bud (from the mesonephric duct) forms ureter, pelvis, calyces and collecting ducts; metanephric mesoderm forms the nephrons. Nephrogenesis ends at 34–36 weeks. Ascent is apparent, from growth of the lumbar and sacral regions.
- Duplex kidney and ureter: caused by early splitting of the ureteric bud (bifid ureter) or two separate buds (complete duplication). In complete duplication the upper-moiety ureter opens lower and more medially (ectopic, often obstructed, with a ureterocele; in girls it may open below the sphincter or into the vagina, causing constant dribbling with otherwise normal voiding). The lower-moiety ureter refluxes (Weigert–Meyer rule).
- Horseshoe kidney: lower poles fused; ascent stopped by the inferior mesenteric artery. Pelvic kidney: supplied by the common iliac artery. Malrotation: hilum faces forwards.
- Retrocaval ureter: reversed-J swing of the upper right ureter at L3. Simple ureterocele: cobra-head with a lucent halo. Renal agenesis often accompanies a Müllerian anomaly on the same side.
Ureter
- 25–30 cm long; runs on psoas over the tips of the transverse processes, crossed in front by the gonadal vessels, and enters the pelvis in front of the common iliac bifurcation; in the pelvis it passes under the uterine artery about 1.5–2 cm lateral to the cervix.
- Narrowings: PUJ, pelvic brim, vesicoureteric junction (narrowest, commonest site for a stone to lodge). Obstruction raises pressure, dilates the system above and, if prolonged, causes pressure atrophy of the papillae and cortex (hydronephrosis).
- Colic is referred T11–L2, loin to groin, labium or scrotum (genitofemoral nerve).
- Blood supply runs longitudinally in the adventitia (from the medial side above the brim, lateral side in the pelvis); stripping it causes ischaemic stricture.
Renal masses and infections on imaging
| Lesion | Imaging clue | Key pathology |
|---|---|---|
| Wilms tumour (age 2–5) | Solid intrarenal mass with a claw of stretched kidney around it; displaces vessels | WT1, 11p13 (WAGR: Wilms, aniridia, genital anomalies, retardation); Beckwith–Wiedemann involves 11p15 |
| Congenital mesoblastic nephroma | Solid mass seen antenatally or under 3 months, concentric rings | Commonest solid renal tumour of the neonate |
| ADPKD | Large kidneys replaced by innumerable bilateral cysts; liver cysts | PKD1, chromosome 16 (85%); berry aneurysms, so subarachnoid haemorrhage |
| Von Hippel–Lindau | Bilateral cysts with multiple enhancing solid masses, pancreatic cysts | VHL (3p) loss; clear cell carcinoma, phaeochromocytoma, cerebellar haemangioblastoma (screen with brain MRI) |
| Oncocytoma | Well-defined, homogeneous, central stellate scar | Benign; cells packed with mitochondria (granular eosinophilic), from intercalated cells; chromophobe carcinoma shares this origin |
| Emphysematous pyelonephritis | Gas in the parenchyma and perirenal space | Uncontrolled diabetes; gas-forming E. coli; gas only in the collecting system (pyelitis) is milder |
| Xanthogranulomatous pyelonephritis | Enlarged non-functioning kidney, staghorn stone, dilated calyces like a bear paw | Proteus infection; yellow nodules of lipid-laden foamy macrophages, which can mimic clear cell carcinoma |
Adrenal glands
- On CT: inverted Y or V shapes. Right adrenal lies directly behind the IVC, with liver lateral and the right crus medial; left lies anteromedial to the upper pole of the left kidney, behind pancreas and splenic vessels.
- Arteries: superior (inferior phrenic), middle (aorta), inferior (renal). Veins: right to the IVC directly (short, so tears easily at surgery), left to the left renal vein.
- Cortex from mesoderm (coelomic epithelium, beside the gonadal ridge, so rests occur in the broad ligament or testis); medulla from neural crest, supplied by preganglionic sympathetic fibres. The fetal zone is large and makes DHEA sulfate, which the placenta converts to oestriol; it involutes after birth.
| Zone | Product | Tumour or imaging link |
|---|---|---|
| Glomerulosa | Aldosterone (driven by angiotensin II and K+) | Conn adenoma: low-HU nodule, high aldosterone, suppressed renin, low K+ |
| Fasciculata | Cortisol (driven by ACTH) | Cortisol-secreting adenoma: ACTH undetectable, so the opposite gland and adjacent cortex atrophy |
| Reticularis | Adrenal androgens | Virilising tumours |
| Medulla | Adrenaline, noradrenaline | Phaeochromocytoma: bright on T2, MIBG avid |
- Lipid-rich adenoma: abundant intracellular lipid makes it under 10 HU unenhanced and causes signal loss on opposed-phase MRI (fat and water in the same voxel cancel). About a third of adenomas are lipid poor and need washout CT (adenomas wash out rapidly).
- Myelolipoma: macroscopic fat (strongly negative HU). Metastasis (lung commonest): over 10 HU, slow washout, often bilateral and heterogeneous; even in a cancer patient, a small nodule is still often an adenoma.
- Addison disease: autoimmune adrenalitis gives small, non-calcified glands; tuberculosis gives enlarged glands early and small, densely calcified glands late (common in Pakistan). Rifampicin speeds cortisol breakdown, so replacement doses must rise.
Remember Hilum front to back: vein, artery, pelvis. Upper-moiety ureter obstructs, lower-moiety ureter refluxes.
Exam trap The commonest site for a ureteric stone to lodge is the vesicoureteric junction, not the pelvic brim.
Exam trap Primary hyperaldosteronism has low renin; high renin with high aldosterone points to renal artery stenosis.
How FCPS asks about this
- Arteries arching over the bases of the pyramids: arcuate arteries, at the corticomedullary junction.
- Straight tubules running up into the cortex: medullary rays; cortex dipping between pyramids is a renal column.
- Embryological cause of a duplex kidney: split or double ureteric bud; upper moiety obstructs, lower refluxes.
- Adrenal adenoma under 10 HU with opposed-phase signal loss: high intracellular lipid.
- Conn adenoma zone: zona glomerulosa; renin suppressed, potassium low.
- Captopril renography change: loss of angiotensin II efferent arteriolar tone in the stenotic kidney.
- Hypertension after a subcapsular haematoma (Page kidney): renin from the compressed kidney.
Test yourself on this topic
5 of the 107 questions in our bank on this topic. Choose an answer to see why every option is right or wrong.
A 19-year-old man has attacks of left loin pain after drinking large amounts of fluid, from obstruction at the pelviureteric junction. At pyeloplasty a vessel from the aorta crosses in front of the junction to reach the lower pole of the kidney. What is this vessel most likely to be?
Answer: Accessory lower-pole renal artery
Dilatation of the pelvis and calyces that stops at the pelviureteric junction is PUJ obstruction. In some patients an accessory (aberrant) renal artery to the lower pole crosses in front of the junction and kinks it, especially when urine flow is high, as after a fluid load. Accessory renal arteries are common because the kidney receives a series of new arteries from the aorta as it ascends, and the lower ones may persist instead of regressing. They are end arteries, so dividing one causes infarction of the segment it supplies.
PUJ obstruction
- Dilated pelvis and calyces, normal ureter
- Pain after fluid load
- Cause: intrinsic narrowing or crossing lower-pole vessel
- Accessory arteries = persistent embryonic arteries
Remember Big pelvis, thin ureter: think PUJ and a crossing vessel.
Exam trap Accessory renal arteries are end arteries, so they cannot simply be tied without losing renal tissue.
Why the other options are wrong
- Left gonadal (testicular) vein Runs down on psoas to the gonad; it does not enter the lower pole.
- Inferior mesenteric artery Arises from the aorta at L3 and supplies the hindgut, not the kidney.
- Ascending branch of left colic artery A branch of the IMA running to the descending colon.
- Second left lumbar artery Runs backwards to the posterior abdominal wall, not to the kidney.
A 70-year-old man with atrial fibrillation has a renal infarct from an embolus to a segmental artery. A thin rim of cortex just beneath the capsule over the infarct survives. What keeps this rim perfused?
Answer: Collateral flow from capsular arteries
Renal segmental and interlobar arteries are end arteries, so an embolus produces a wedge-shaped infarct. The outermost few millimetres of cortex, however, also receive blood from capsular arteries, which arise from the renal artery and anastomose with branches of the suprarenal, gonadal and lumbar arteries. This collateral supply keeps a thin subcapsular rim alive, seen on contrast CT as the cortical rim sign.
Subcapsular rim
- Wedge-shaped infarct (end arteries)
- Thin subcapsular rim survives
- Rim fed by capsular arteries
- Collaterals from suprarenal, gonadal, lumbar
Remember Infarct with a rim: the capsule has its own supply.
Exam trap The same capsular supply keeps a subcapsular rim alive in renal cortical necrosis.
Why the other options are wrong
- Retrograde flow in the renal vein Venous blood does not perfuse the cortex in this way.
- Diffusion of contrast from the pelvis Contrast in the pelvis does not diffuse into cortex.
- Persisting flow in arcuate arteries Arcuate arteries in the infarcted segment are blocked with their parent artery.
- Lymphatic flow from the hilum Lymph does not carry contrast to the cortex.
A 6-year-old girl voids normally but is damp all day. She has a complete duplex right kidney with a dilated upper moiety. According to the usual pattern in complete duplication, which ureter opens ectopically below the bladder neck?
Answer: Upper-pole moiety ureter
In complete ureteric duplication the Weigert-Meyer rule applies: the ureter from the upper pole moiety inserts lower and more medially than the lower-pole ureter. It may end ectopically below the bladder sphincter (in girls in the urethra or vagina), causing constant dribbling despite normal voiding, and it is prone to obstruction and ureterocele. The lower-pole ureter enters higher and more laterally, with a short intramural course, so it tends to reflux. A common stem only exists in incomplete duplication.
Weigert-Meyer rule
- Upper moiety ureter: low, medial, may be ectopic
- Upper moiety: obstruction, ureterocele
- Lower moiety ureter: high, lateral
- Lower moiety: reflux
Remember Upper obstructs, lower refluxes.
Exam trap Boys with an ectopic ureter are not wet, because it always opens above the external sphincter.
Why the other options are wrong
- Lower-pole moiety ureter Inserts high and lateral; tends to reflux rather than open ectopically.
- Left single ureter Normal on the other side here.
- Persistent urachus Leaks urine at the umbilicus, not the perineum.
- Common stem of both ureters Seen in incomplete duplication, which joins above the bladder.
A 60-year-old woman is confused, febrile and hypotensive with left loin pain. Emergency nephrectomy shows a necrotic kidney with gas bubbles in its parenchyma, and culture grows E. coli. Which underlying condition most strongly predisposes to this infection?
Answer: Uncontrolled diabetes mellitus
Gas within the renal parenchyma in a septic patient is emphysematous pyelonephritis, a necrotising infection usually caused by Escherichia coli or Klebsiella. About 90% of patients have diabetes mellitus, often poorly controlled. High tissue glucose allows the bacteria to ferment sugar and produce carbon dioxide and hydrogen, while diabetic microvascular disease impairs blood supply and the removal of gas. Obstruction is an additional risk factor in non-diabetic patients.
Emphysematous pyelonephritis
- Gas in renal parenchyma
- Usually diabetic patients
- Organisms: E. coli, Klebsiella
- High glucose: bacteria ferment and form gas
Remember Gas in the kidney of a septic diabetic: emphysematous pyelonephritis.
Exam trap Gas confined to the collecting system (emphysematous pyelitis) carries a much better prognosis than gas in the parenchyma.
Why the other options are wrong
- Vesicoureteric reflux Causes reflux nephropathy and scarring, not gas-forming infection.
- Chronic alcohol misuse Not the main association.
- Normal pregnancy Predisposes to ordinary pyelonephritis through ureteric dilatation, not to gas formation.
- Long-term proton pump inhibitor use Linked to enteric infections, not renal gas.
An IVU in a 30-year-old woman shows a rounded, contrast-filled dilatation of the lower end of the left ureter projecting into the bladder, surrounded by a thin lucent halo, giving a cobra-head appearance. What is the most likely diagnosis?
Answer: Simple ureterocele
A ureterocele is a cystic dilatation of the submucosal (intravesical) segment of the distal ureter. On urography it fills with contrast and bulges into the bladder, and the thin wall of ureter and bladder mucosa around it shows as a lucent halo, giving the cobra-head or spring-onion sign. A simple (orthotopic) ureterocele in an adult is usually at the normal ureteric opening, whereas an ectopic one is typically linked to the upper moiety of a duplex kidney in children.
Ureterocele
- Cystic dilatation of intravesical ureter
- Cobra-head sign on IVU
- Lucent halo = ureteric wall + mucosa
- Ectopic ones: upper-pole moiety of duplex kidney
Remember Cobra head in the bladder: ureterocele.
Exam trap A stone impacted at the ureteric opening can give a pseudo-ureterocele with a thick, irregular halo.
Why the other options are wrong
- Bladder diverticulum An outpouching of the bladder wall outside the bladder outline.
- Vesicoureteric reflux Shows contrast passing up the ureter on a voiding study, not a filling bulge.
- Primary megaureter Dilatation of the ureter above a narrow segment; it does not bulge into the bladder.
- Bladder transitional cell tumour A filling defect that does not contain contrast.
Where this sits in the CPSP syllabus
- Diagnostic Radiology, Paper 2: Abdomen, Kidneys, ureters and adrenal glands
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