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Renal Papillary and Calyceal Lesions on CT Urography

Renal Papillary and Calyceal Lesions on CT Urography

Satomi Kawamoto, M.D

The Russell H. Morgan Department of Radiology and Radiological Science and Department of Pathology
Johns Hopkins Medical Institutions
Baltimore, MD USA

 

Purpose/Educational Goals

  • To review normal anatomy and anatomical variations of renal papilla and calyces on CT urography.
  • To review and illustrate appearance of calyceal and papillary lesions on CT urography, and techniques to influence their detection.

 

Outline

  • Normal appearance of renal papillae and calyces
    • Anatomy and physiology, papillary/calyceal pathology
    • Normal appearances and variations of papillae and calyces
    • Normal papillary blush
  • Medullary/papillary lesions:
    • Benign tubular ectasia/medullary sponge kidney
    • Medullary nephrocalcinosis
    • Papillary necrosis
  • Calyceal lesions
    • Calyceal diverticulum
    • Infection/inflammation
    • Forniceal rupture, fistula
    • Urothelial neoplasm

 

Renal Vascular and Renal Tubular Anatomy

Renal Vascular and Renal Tubular Anatomy

 

Normal Renal Enhancement on CT

Normal Renal Enhancement on CT

 

Normal Anatomy of Renal Collecting System

Normal Anatomy of Renal Collecting System

 

Normal Papillary Blush

Normal papillary blush in an asymptomatic patient. (A) Early excretory phase axial CT in soft tissue window, and (B) axial and (C) coronal wide window images show indistinct, prominent papillary opacity in “blushlike” appearance (arrows), representing normal concentration of contrast in the medulla.
Normal papillary blush is accentuated with low-osmolality contrast media (less fluid is excreted into the tubular lumen, therefore the concentration of contrast material is higher than with high-osmolality contrast material).

Normal Papillary Blush

 

Benign Tubular Ectasia

55-year-old man with benign tubular ectasia, presented with microscopic hematuria. Excretory phase CT images show distinct, linear, “paintbrush”-like collections of contrast (arrows) in the dilated collecting ducts in the renal pyramids, which are difficult to appreciate on soft tissue window (A), and better appreciated in wide window image (B) and coronal MIP image (C).

Benign Tubular Ectasia

 

Medullary Sponge Kidney

40-year-old man with history of renal stones and hematuria. (A) Noncontrast CT shows a small calcification in the papilla (red arrow). (B) Excretory phase CT in soft tissue window shows no obvious abnormality. However, in wide window image (C) and coronal MIP image (D) show “paintbrush” appearance of the medullary pyramids (yellow arrows) due to pooling of contrast within the dilated collecting ducts, a finding typical of medullary sponge kidney.

Medullary Sponge Kidney

 

Benign Tubular Ectasia/Medullary Sponge Kidney

  • A condition characterized by dilatation of the renal collecting ducts in the papillae.
    • Benign tubular ectasia: isolated finding of linear contrast collections
    • Medullary sponge kidney: linear contrast collections associated with urolithiasis or medullary calcinosis
  • “Paintbrush”-like appearance of multiple, discrete, linear densities (2-3mm in diameter) in the pyramid.
  • Should not be confused with indistinct normal papillary “blush” due to normal concentration of contrast.
  • Associated with stone disease, hematuria
  • Can involve only one, a few, or all of the calyces.
  • Bilateral in 60-80% of cases

 

Medullary Nephrocalcinosis

40-year-old male with prior resection of parathyroid carcinoma, presented with lung metastases and recurrent hyperparathyroidism. (A) Axial and (B) coronal noncontrast CT show multiple calcifications in the medulla. (C) Diffuse demineralization of pelvic bones. (D, E) Multiple lung metastases (arrows).
Parathyroid carcinoma is less than 1% of all causes of hyperparathyroidism.

Medullary Nephrocalcinosis

 

Medullary Nephrocalcinosis

40-year-old woman with renal tubular acidosis type 1 (distal). History of renal stones, recurrent urinary tract infections (UTIs), presented with right flank pain. (A) Noncontrast axial soft tissue window and (B) wide window images, and (C) coronal postcontrast MIP image show massive calcifications in the renal medulla. Calculus filling the upper pole calyx (yellow arrow) is also seen. (D) Scout image shows multiple calculi in the distal right ureter (yellow arrows).

Renal tubular acidosis Type 1 (distal)
  • Defective proton secretion from the distal tubules leading to systemic acidosis.
  • Hypercalciuria develops to compensate for the hydrogen cation secretion deficiency.
  • When massive medullary nephrocalcinosis is seen, renal tubular acidosis is usually the underlying cause.
Medullary Nephrocalcinosis

 

Medullary Nephrocalcinosis

  • Medullary nephrocalcinosis: Deposition of calcium salts in the medulla (in the interstitium or in the tubules)
  • Common causes
    • Hyperparathyroidism: most common cause in adults
    • Medullary sponge kidney
    • Renal tubular acidosis type 1 (distal)
    • Other conditions with hypercalcemic and hypercalciuric status, papillary necrosis
  • Nephrocalcinosis: Formation of dystrophic calcifications within the renal parenchyma
  • Urolithiasis: Stones within the lumen of the urinary tract
    • Significant overlap between nephrocalcinosis and urolithiasis
    • Calculi within the renal medulla/distal tubules may erode into the collecting system.

 

Papillary Necrosis

Papillary Necrosis

 

Renal Abscess and Papillary Necrosis

46-year-old woman with history of multiple prior UTIs, presented with renal abscess. (A) Coronal excretory phase CT shows renal abscess (blue arrow). (B) Axial excretory phase soft tissue window and (C) wide window images, as well as (D) coronal MIP image show dilated blunted upper pole calix (red arrow) with multiple collections of contrast in “ball on tree” appearance (yellow arrows) representing papillary necrosis. Wide window and MIP images better demonstrate contrast collections than soft tissue window.

Renal Abscess and Papillary Necrosis

 

Papillary Necrosis with Sloughed Papilla

Papillary Necrosis with Sloughed Papilla

 

Renal and Urinary Tract Tuberculosis

Renal and urinary tract tuberculosis (Tbc). (A) Coronal nephrographic phase image shows thickening and blunting of the upper pole calyx with adjacent cortical scarring (arrow). (B) Axial excretory phase image shows small contrast collection in the area of papilla (arrow), indicating small papillary necrosis. (C) Excretory phase coronal and (D) oblique sagittal images show diffuse irregular wall thickening and enhancement of the left ureter and bladder with long-segment ureteral narrowing. (Images curtesy of Dr. Zubair Kazi, Consultant Radiologist, Saifee Hospital)

Genitourinary tuberculosis (Tbc):
  • Accounting for 15–20% of tuberculous infections outside lungs
  • Renal Tbc results from hematogenous seeding of bacilli in the glomerular and peritubular capillary bed. It forms granulomas, leading to caseous necrosis and cavitation.
  • Regional spread of bacilli causes seeding of the bacilli into the renal pelvis, ureters and bladder.
Renal and Urinary Tract Tuberculosis

 

Papillary Necrosis

  • Renal medulla and papillae are vulnerable to ischemic necrosis because of unique arrangement of their blood supply and the local interstitial hypertonicity.
  • Risk factors:
    • Diabetes mellitus
    • Analgesic abuse
    • High-dose nonsteroidal anti-inflammatory drugs
    • Sickle cell anemia
    • Chronic infection (such as tuberculosis and pyelonephritis)
    • Others: Acute urinary obstruction, Renal vein thrombosis, Chronic alcoholism
  • Compromised perfusion: Vascular spasm, Compression, Vasculitis, Hemoglobinopathy
  • Varies greatly in severity and rate of progression
  • +/- Hematuria, decreased renal function

 

Papillary Necrosis

Papillary Necrosis

 

Calyceal Diverticulum

20-year-old woman with recent history of UTI. (A, B) Axial CT images in late corticomedullary phase shows complex cystic lesion (yellow arrows) in the right kidney, containing a calcification (blue arrow). Excretory phase axial images (C, D) and MIP image (E) show contrast accumulation within the cystic lesion (yellow arrows) surrounding the calcification (blue arrow), representing a calyceal diverticulum with a calculus.

Calyceal Diverticulum

 

Calyceal Diverticulum

Calyceal Diverticulum

 

Hydronephrosis and Forniceal Rupture

85-year-old male with colon cancer with pelvic metastasis resulting in right hydronephrosis. (A) Axial late nephrographic phase CT shows right hydronephrosis with decreased contrast enhancement of the right kidney compared to the left. (B) Axial, (C) coronal, and (D) sagittal excretory phase CT images show contrast leakage from calyceal fornix, with extravasated contrast surrounding the right renal pelvis and proximal ureter (yellow arrows). Contrast excretion within the renal calyces is also seen (red arrows).

Hydronephrosis and Forniceal Rupture

 

Forniceal Rupture

  • Obstructing collecting system can decompress spontaneously by leakage of urine, typically from one or more calyceal fornices.
  • Calyceal fornix is the weakest point of the renal collecting system.
  • Extravasated contrast may surround the renal pelvis and proximal ureter on excretory phase CT urography.
  • Common causes: Obstruction by distal ureteric stones, followed by malignant extrinsic ureteric compression.
  • The patient’s symptoms may improve abruptly due to decompression.
  • Forniceal rupture due to acute obstruction usually has no clinical significance if the urine is not infected.

 

Xanthogranulomatous Pyelonephritis (XGP) with Ruptured Calyx and Perinephric and Intrathoracic Extension

42-year-old woman with XGP, presented with chronic left flank pain. (A) Coronal contrast enhanced CT shows poorly functioning left kidney with a large obstructing calculus (blue arrows) and large central hypodense areas due to dilated collecting system, representing XGP. (B, C) Axial and (D) oblique sagittal contrast enhanced CT show perirenal abscess (yellow asterisk) through the calyceal defect (yellow arrow) with intrathoracic extension (red asterisk). Additional perirenal abscess is also seen more inferiorly (blue asterisk).

Xanthogranulomatous Pyelonephritis :
  • Rare chronic renal infection
  • End stage of longstanding obstructive pyelonephritis
  • Diffuse infiltration by lipid-laden macrophages (xanthoma cells)
  • Enlarged kidney, diffuse form>focal/segmental form
  • Centrally obstructing calculus (>70%)
  • Extension of inflammation (perirenal/pararenal space, psoas muscle).
  • DDx: hydronephrosis, avascular tumor
Xanthogranulomatous Pyelonephritis (XGP) with Ruptured Calyx and Perinephric and Intrathoracic Extension

 

Pyonephrosis and Fistulous Connection between Renal Calyx and Perinephric/Abdominal Wall Abscess

56-year-old woman with history of renal calculi and recurrent UTIs, who presented with urosepsis. (A) Oblique coronal, (B) axial, and (C) oblique sagittal contrast enhanced CT images show obstructing distal ureteral calculi (green arrow) with hydronephrosis. Fistulous connection (yellow arrow) from the dilated calyx to perinephric and abdominal wall abscess (red arrows) containing a calculus (B: blue arrow). Multiple renal calculi are also seen in the dilated calyces (blue arrows). (D) Longitudinal gray-scale ultrasonography shows layering debris (yellow arrows) within the dilated renal collecting system, suggesting presence of pus.

Xanthogranulomatous Pyelonephritis (XGP) with Ruptured Calyx and Perinephric and Intrathoracic Extension

 

Pyonephrosis

  • Infected purulent urine in an obstructed collecting system.
  • With “pus under pressure”, patients may deteriorate rapidly and become septic.
  • Prompt diagnosis and treatment are necessary.
    • Decompression and drainage (percutaneous or retrograde nephrostomy)
    • Eliminate the obstruction
  • Complications
    • Psoas abscess, perinephric abscess
    • Generalized peritonitis from interaperitoneal rupture
    • Renocolonic, renoduodenal, renocutaneus fistulae
  • Some cases of chronic pyonephrosis have clinical, imaging, and pathologic overlap with XGP.

 

Acute Pyelonephritis, Pyelitis, Ureteritis, Cystitis

40-year-old woman with HIV and UTI. Urine culture grew E.coli. (A) Coronal corticomedullary phase CT image shows diffuse wall thickening of calyces and renal pelves (yellow arrows) representing pyelitis. Wedge shaped hypodense lesions in the right kidney (red arrows) representing acute pyelonephritis. (B, C) Axial arterial phase and (D) excretory phase images show diffuse thickening of the ureters (yellow arrows) and bladder (red arrow) with mucosal enhancement due to ureteritis and cystitis.

Acute Pyelonephritis, Pyelitis, Ureteritis, Cystitis

 

Acute Pyelonephritis, Emphysematous Pyelitis

58-year-old woman with history of diabetes mellitus, nausea, vomiting, and right upper quadrant pain. (A, B) Axial contrast enhanced CT in delayed phase (several hours after IV contrast administration) show enlarged right kidney with hydronephrosis, and delayed excretion of contrast from the right kidney due to obstructing distal right ureteral calculus (not shown). Air within the lumen and wall of the right renal collecting system (yellow arrows). Multifocal areas of decreased enhancement (red arrows) related to acute pyelonephritis.
E. Coli grew in the blood and urine cultures. The patient underwent right nephrectomy. Perinephric abscess and severe multifocal acute pyelonephritis were found pathologically.

Acute Pyelonephritis, Emphysematous Pyelitis

 

Emphysematous Pyelonephritis

  • Emphysematous Pyelonephritis: Gas forming infection within or around the kidneys.
  • Huang-Tseng CT classification of emphysematous pyelonephritis
    • Class I: Gas in collecting system only (“Emphysematous pyelitis”). Better prognosis, often managed with IV antibiotics only
    • Class II: Gas in renal parenchyma only
    • Class III: Extension of gas or abscess or perinephric space (3a) or pararenal space (3b)
    • Class IV: Bilateral emphysematous pyelonephritis or solitary kidney with emphysematous pyelonephritis

 

Renal Atrophy and Calyceal Clubbing

21-year-old woman with spina bifida, neurogenic bladder, status post bladder augmentation at age 7 with multiple revisions and ureteral re-implant. Recurrent stones and UTIs. (A) Axial corticomedullary phase, and (B) axial and (C) coronal excretory phase images show atrophic right kidney with severe parenchymal scarring with loss of medulla and cortex over the calyceal clubbing (arrows). Irregular bladder contour (asterisk) due to multiple prior surgeries.

Renal Atrophy and Calyceal Clubbing

 

Urothelial Carcinoma

89-year-old woman presented to emergency room for gross painless hematuria. (A) Axial and (B) coronal corticomedullary phase images show a subtle enhancing mass in the lower pole calyceal region. The mass encases and narrows the lower pole calyx on excretory phase (C) axial and (D) coronal CT. Pathology revealed high grade urothelial carcinoma which invaded deeply into the renal cortex to within 2 mm of the renal capsule (pT3).

Urothelial Carcinoma

 

Multifocal Urothelial Carcinomas

63-year-old man with history of bladder cancer. Multifocal urothelial carcinomas of the right renal collecting system. (A, B) Axial corticomedullay phase images shows a mass in the upper pole calyx (yellow arrow in Figure A) and mid pole calyx (red arrow in Figure B). On excretory phase axial images (C, D) and anterior volume rendered image (E), these masses are seen as filling defects (yellow and red arrows). Additional multiple filling defects are also present in the renal collecting system (arrowheads in Figure E). The patient underwent right ureteronephrectomy, which revealed multifocal papillary urothelial carcinomas.

Multifocal Urothelial Carcinomas

 

Urothelial Neoplasm

  • Upper urinary tract urothelial neoplasm accounts for approximately 5% of all urothelial neoplasms.
  • Assessment of the entire urothelium is essential before treatment because of its multicentric nature.
    • 2% of patients with bladder carcinoma have synchronous upper tract urothelial carcinoma.
    • 6% of patients with bladder carcinoma will have metachronous upper tract urothelial carcinoma.
    • 40% of patients with upper tract urothelial carcinoma will have bladder cancer.
  • CT appearances of urothelial neoplasm of the upper urinary tract
    • A focal intraluminal mass
    • Urothelial wall thickening with luminal narrowing
    • An infiltrating mass
  • Urothelial neoplasm may enhance after IV contrast administration, which can help to differentiate urothelial neoplasm from stone or clot.
  • Uncommonly, punctate, linear or granular calcifications may be seen.

 

Summary

  • CT urography is a current modality of choice for evaluation of painless gross or microscopic hematuria.
  • Routine use of wide window setting to view excretory phase CT is critical to detect subtle lesions in the renal papillae and calyces.
  • The coronal plane often essential to perceive the subtle changes in the pelvocalyceal anatomy and narrow the differential diagnosis or make the correct diagnosis.

 

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Acknowledgements

  • Satomi Kawamoto, M.D
  • Peter Duggan, M.D.
  • Sheila Sheth, M.D.
  • Hiroshi Miyamoto, M.D.
  • Elliot K. Fishman, M.D.

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