eMedicine Specialties > Urology > Infections and Related Inflammatory Conditions

Papillary Necrosis: Workup

Author: Jeffrey M Donohoe, MD, Assistant Professor of Pediatric Urology, Department of Surgery, Division of Urology, Medical College of Georgia
Coauthor(s): Jack H Mydlo, MD, Chief, Department of Urology, Woodhull Hospital; Chair and Professor, Department of Urology, Temple University School of Medicine
Contributor Information and Disclosures

Updated: Jan 9, 2008

Workup

Laboratory Studies

  • The general diagnostic studies include a urinalysis (ie, routine, microscopic), a complete blood cell count, a complete metabolic panel, and prothrombin time and activated partial thromboplastin time determinations. If patients have concomitant fever, obtain urine and blood cultures under sterile conditions. If patients are prostrate and obtunded, measure arterial blood gases and perform standard electrocardiography and chest radiography. If acute obstruction is suspected, perform renal ultrasonography or another radiographic evaluation and request an immediate consultation with a urologist.
  • Patients who present with hematuria, even if diagnostic interventions indicate papillary necrosis, require a full urologic workup for their hematuria because they may have a concomitant bladder tumor or similar lesion.
    • Perform a routine and microscopic urinalysis from properly collected specimens (ie, sterile catheterization, clean-catch midstream).
    • Perform a urine culture obtained via sterile catheterization or clean-catch midstream.
    • Obtain a urine cytology study on a voided specimen.
    • Perform an imaging study, preferably with intravenous contrast, to evaluate the upper urinary tract. UseCT scanning or intravenous urography (IVU), depending on preference. Perform the imaging study prior to cystoscopy because if the study is limited or incomplete, a urologist may need to perform bilateral retrograde pyelography (RPG) in addition to routine cystoscopy. The test of choice to evaluate the upper tracts of patients with contraindications to intravenous contrast is a bilateral RPG.
    • If necessary, perform a cystoscopy (ie, flexible or rigid) with bilateral RPGs.
    • Ureteroscopy may be indicated if the RPG reveals a filling defect in either collecting system. Do not dismiss any persistent collecting system filling defect as a sloughed papilla or blood clot until certain it is not a urothelial papillary tumor or radiolucent stone.
  • The most common urinalysis findings include proteinuria, pyuria, bacteriuria, and low urine-specific gravity. More than 50% of patients develop leukocytosis and azotemia.
  • An acutely elevated serum creatinine level indicates that the offending process is either bilateral or unilateral. This process can be obstructive or may be the manifestation of some toxic, metabolic, or inflammatory insult.
  • Patients with known or possible obstruction require an urgent consultation with a urologist.
  • If the clinical picture is suggestive, investigate for any of the conditions associated with renal papillary necrosis, including pyelonephritis, obstructed urinary tract, hemoglobinopathies, tuberculosis, liver cirrhosis, analgesic abuse, renal transplant rejection, and diabetes mellitus.
  • Clinical findings may also prompt performing hemoglobin electrophoresis, a subdermal tuberculin test, liver function tests, serum ammonium measurements, serum and urine salicylate and acetaminophen levels, a hemoglobin A1c measurement, and cyclosporin or tacrolimus levels.

Imaging Studies

  • For representative images, refer to Papillary Necrosis in the Radiology section of the eMedicine journal.
  • Radiography
    • Standard radiography of the abdomen that visualizes the span of the kidneys, ureters, and bladder is very good for visualizing radiopaque calculi and may offer hints as to whether the patient has 2 kidneys. However, this imaging modality neither yields information on the integrity of the urinary tract nor helps to diagnose hydronephrosis or to elucidate kidney function.
    • Thus, plain radiography is not paramount because it is generally not diagnostic for renal papillary necrosis. Much better radiographic tools are available for this purpose.
  • CT scanning
    • If the clinical scenario suggests acute obstruction, CT scanning is the imaging modality of choice, mostly because it is extremely accurate for diagnosing calculi—one of the prime differential diagnoses of a sloughed papilla.
    • A CT scan also shows the entire anatomy of the collecting system and easily reveals hydronephrosis, inflammatory changes, and purulent collections, all without the administration of intravenous contrast. With the administration of contrast and delayed films, if necessary, clinicians can easily visualize filling defects. Contrast images also provide a good, albeit unquantified, estimate of cortical function.
    • CT scans can also be used to accurately diagnose renal papillary necrosis. Historically, subsequent verification via IVU was required. However, Lang et al have shown that they can identify papillary and medullary necrosis at an early and reversible stage using multiphasic helical CT scanning.7,8 When adequately treated with antibiotics, reperfusion improved in approximately 60% of patients within 3 months.
    • When intravenous contrast is contraindicated, CT scanning without contrast may be ideal for diagnosing acute obstruction, estimating renal function, and, most importantly, excluding nephrolithiasis or ureterolithiasis. Ultrasonography has similar capabilities but, without high-grade obstruction, is not as sensitive for diagnosing calculi. Although less expensive and less invasive (ie, no radiation exposure), ultrasonography is operator-dependent and less sensitive for diagnosing calculi. A bilateral RPG is preferred in patients with contraindications to intravenous contrast and in those in whom the urinary tract must indispensably be opacified.
    • CT findings include (1) small kidneys, (2) ring shadows in the medullae, (3) contrast-filled clefts in the renal parenchyma, and (4) renal pelvic filling defects.
    • Lang et al describe the ischemic changes of early medullary and papillary necrosis as "a circumscribed, yet often poorly marginated area of diminished enhancement in the tip of the medullary period." They claim these changes can be seen on scans taken in the early corticomedullary phase but are best seen on scans taken in the nephrographic phase.7,8
  • Intravenous urography with nephrotomography
    • This modality provides an excellent display of the anatomy; even very minor morphological changes in the urinary tract are precisely documented.
    • IVU is typically the imaging method of choice for diagnosing renal papillary necrosis, although it has its limitations. Clear IVU imaging largely depends on a paucity of stool or bowel gas, which is usually not the case, meaning that images can be obscured. Additionally, approximately 15% of calculi are not radiopaque; thus, IVU is not the best initial test in patients who present with colic, in whom stones are more common and who require a different workup and treatment plan. In addition, in severe cases, renal function may be so poor that diagnostic changes cannot be demonstrated. Lastly, IVU is contraindicated in patients with azotemia and in patients with coexisting diseases, particularly allergy, asthma, dehydration, diabetes mellitus, thyrotoxicosis, and plasmocytoma. With the advances in CT imaging and the limitations of IVU, many clinicians and radiologists consider CT scan the imaging modality of choice for renal papillary necrosis.
    • If, for any reason, IVU is not the best choice, contrast-enhanced CT scanning, with its far superior contrast resolution, may demonstrate necrotic detached papillae within medullary cavities, thus establishing the diagnosis.
    • IVU findings include (1) shrinkage and irregularity of papillae, with consequent widening of calyceal fornices, creating what are described as hooks and spurs; (2) desquamated papilla in situ, demarcated by contrast material as a ring shadow, often in a triangular shape (commonly referred to as the ring sign); (3) a calix without a papilla; (4) a partially calcified filling defect in the renal pelvis (ie, sequestered papilla); and (5) contrast-containing rice-grain–sized cavities in the papilla, which are pathognomonic for the medullary form of renal papillary necrosis.
  • Renal ultrasonography
    • This imaging modality is safe, quick, inexpensive, noninvasive, and diagnostic for hydronephrosis, certain anomalies, and stones large enough to provide a shadow. It is also operator-dependent, which should be taken into consideration.
    • Ulreich could not duplicate his IVU-confirmed diagnosis of renal papillary necrosis when reviewing the sonograms of the same patients.9
    • Vijayaraghavan et al describe sonographic features of necrotic sloughed papillae representing filling defects in the ureter.10 In one third of their patients, necrosed papillae were visualized in cavities in the medullary region communicating with the calyces.
    • Ultrasonography findings may suggest the diagnosis late in the course of the disease but is not sensitive enough to be confirmatory in the earlier, more reversible phases of renal papillary necrosis.
  • Retrograde pyelography
    • Images may reveal a clubbed calyx or a filling defect in the ureter.
    • This test is more invasive because it requires endoscopic access.
    • Precautions such as intravenous antibiotic prophylaxis must be taken because this procedure involves retrograde introduction of contrast, which can increase intrapelvic pressure and may lead to pyelovenous backflow of infectious material, thus predisposing the patient to sepsis. Gentle slow introduction of contrast decreases the likelihood of this complication, but intravenous antibiotics are warranted nonetheless.

Diagnostic Procedures

  • Although CT scanning, IVU, and ultrasonography findings can suggest the diagnosis of renal papillary necrosis, urologic intervention confirms the diagnosis and excludes other obstructing agents (ie, tumors, stones, blood clots). See Surgical therapy.

Histologic Findings

The characteristic pathologic finding is coagulative infarct necrosis. See Pathophysiology.

More on Papillary Necrosis

Overview: Papillary Necrosis
Workup: Papillary Necrosis
Treatment: Papillary Necrosis
Follow-up: Papillary Necrosis
Multimedia: Papillary Necrosis
References

References

  1. Friedrich N. Ueber necrose der nierenpapillen bei hydronephrose. Virchows Arch A Path Anat. 1877;69:308-12.

  2. Gunther GW. Die papillennekrosen der niere bei diabetes. Munchen Med Wochenschr. 1937;84:1695-9.

  3. Edmondson HA, Martin HE, Evans N. Necrosis of renal papillae and acute pyelonephritis in diabetes mellitus. Arch Intern Med. 1947;79:148.

  4. Spuhler O, Zollinger HU. [Chronic interstitial nephritis.]. Z Klin Med. 1953;151(1):1-50. [Medline].

  5. Mandel EE. Renal medullary necrosis. Am J Med. Sep 1952;13(3):322-7. [Medline].

  6. Simon HB, Bennett WA, Emmett JL. Renal papillary necrosis: a clinicopathologic study of 42 cases. J Urol. Apr 1957;77(4):557-67. [Medline].

  7. Lang EK, Macchia RJ, Thomas R, Davis R, Ruiz-Deya G, Watson RA. Detection of medullary and papillary necrosis at an early stage by multiphasic helical computerized tomography. J Urol. Jul 2003;170(1):94-8. [Medline].

  8. Lang EK, Macchia RJ, Thomas R, Davis R, Ruiz-Deya G, Watson RA, et al. Multiphasic helical CT diagnosis of early medullary and papillary necrosis. J Endourol. Feb 2004;18(1):49-56. [Medline].

  9. Ulreich S. Ultrasound in the evaluation of renal papillary necrosis [letter]. Radiology. Sep 1983;148(3):864. [Medline].

  10. Vijayaraghavan SB, Kandasamy SV, Mylsamy A, Prabhakar M. Sonographic features of necrosed renal papillae causing hydronephrosis. J Ultrasound Med. Sep 2003;22(9):951-6; quiz 957-8. [Medline].

  11. Falkenberg FW, Hildebrand H, Lutte L, Schwengberg S, Henke B, Greshake D, et al. Urinary antigens as markers of papillary toxicity. I. Identification and characterization of rat kidney papillary antigens with monoclonal antibodies. Arch Toxicol. 1996;71(1-2):80-92. [Medline].

  12. Garber SL, Mirochnik Y, Desai SS, Arruda JA, Dunea G. Angiotensin-converting enzyme inhibition reduces the effect of bromoethylamine-induced papillary necrosis and renal fibrosis. J Am Soc Nephrol. Jun 1998;9(6):1052-9. [Medline].

  13. Abe K, Ozono Y, Miyazaki M, Furusu A, Shioshita K, Sasaki O, et al. Prostaglandin E1 for renal papillary necrosis in a patient with diabetes mellitus. J Int Med Res. Mar-Apr 1999;27(2):90-5. [Medline].

  14. Akhund L, Quinet RJ, Ishaq S. Celecoxib-related renal papillary necrosis. Arch Intern Med. Jan 13 2003;163(1):114-5. [Medline].

  15. Barnes DJ. Beethoven's final illness. Lancet. Mar 16 1996;347(9003):766. [Medline].

  16. Bing RJ. Cyclooxygenase-2 inhibitors: is there an association with coronary or renal events?. Curr Atheroscler Rep. Mar 2003;5(2):114-7. [Medline].

  17. Breyer MD, Hao C, Qi Z. Cyclooxygenase-2 selective inhibitors and the kidney. Curr Opin Crit Care. Dec 2001;7(6):393-400. [Medline].

  18. Cotran R, Kumar V, Robbins SL. The kidney. In: Cotran R, Kumar V, Robbins SL, eds. Pathologic Basis of Disease. 5th ed. Philadelphia, Pa: WB Saunders; 1994:964-72.

  19. Davies PJ. Beethoven's nephropathy and death: discussion paper. J R Soc Med. Mar 1993;86(3):159-61. [Medline].

  20. Eknoyan G. Chronic glomerulonephritis and chronic interstitial nephritis. In: Schrier RW, Gottschalk CW. Diseases of the Kidney. Vol. 2. 5th ed. Little Brown and Co: Boston, Mass; 1993:1976-9.

  21. Eknoyan G, Qunibi WY, Grissom RT, Tuma SN, Ayus JC. Renal papillary necrosis: an update. Medicine (Baltimore). Mar 1982;61(2):55-73. [Medline].

  22. Gower PE. A prospective study of patients with radiological pyelonephritis, papillary necrosis and obstructive atrophy. Q J Med. Apr 1976;45(178):315-49. [Medline].

  23. Hagiwara N, Fujihiro S, Deguchi T. [Renal papillary necrosis managed by transurethral procedures: a case report]. Hinyokika Kiyo. Jun 2003;49(6):329-31. [Medline].

  24. Kamath S, Moody MP, Hammonds JC, Wells IP. Papillary necrosis causing hydronephrosis in renal allograft treated by percutaneous retrieval of sloughed papilla. Br J Radiol. Apr 2005;78(928):346-8. [Medline].

  25. Kankuri E, Solatunturi E, Vapaatalo H. Effects of phenacetin and its metabolite p-phenetidine on COX-1 and COX-2 activities and expression in vitro. Thromb Res. Jun 15 2003;110(5-6):299-303. [Medline].

  26. Kovacevic L, Bernstein J, Valentini RP, Imam A, Gupta N, Mattoo TK. Renal papillary necrosis induced by naproxen. Pediatr Nephrol. Aug 2003;18(8):826-9. [Medline].

  27. Lange S. Diseases. In: Lange S, ed. Teaching Atlas of Urologic Radiology. First ed. New York, NY: Thieme Medical; 1995:88-9.

  28. Lange S. Differential Diagnosis: Urographic findings. In: Lange S, ed. Teaching Atlas of Urologic Radiology. First ed. New York, NY: Thieme Medical; 1995:198-203.

  29. Lauler DP, Schreiner GE, David A. Renal medullary necrosis. Am J Med. Jul 1960;29:132-56. [Medline].

  30. Lindvall N. Radiological changes of renal papillary necrosis. Kidney Int. Jan 1978;13(1):93-106. [Medline].

  31. Saifuddin A, Bark M. Case report: computed tomography demonstration of renal papillary necrosis. Clin Radiol. Oct 1991;44(4):275-6. [Medline].

  32. Salo JO, Talja M, Lehtonen T. Ureteroscopy in the treatment of ureteral obstruction caused by papillary necrosis. Eur Urol. 1987;13(1-2):140-1. [Medline].

  33. Sargent JC, Sargent JW. Unilateral renal papillary necrosis. J Urol. May 1955;73(5):757-64. [Medline].

  34. Schaeffer AJ. Infections of the urinary tract. In: Walsh PC, Retik AB, Vaughan ED Jr, eds. Campbell's Urology. Vol. 1. 7th ed. Philadelphia, Pa: WB Saunders; 1998:536-7, 568.

  35. Schwarz A. Beethoven's renal disease based on his autopsy: a case of papillary necrosis. Am J Kidney Dis. Jun 1993;21(6):643-52. [Medline].

  36. Stamm WE. Urinary tract infections and pyelonephritis. In: Isselbacher KJ, Braunwald E, Wilson JD, Martin JB, Fauci AS, Kasper DL, eds. Harrison's Principles of Internal Medicine. Vol. 1. 13th ed. New York, NY: McGraw-Hill; 1994:553.

  37. von Seyfried I. Autopsy protocol of Ludwig van Beethoven, translated from Latin. In: Ludwig van Beethovens Studien im Generalba. 2nd ed. Contrapunkt und in der Compositions: 1852-1853.

  38. Voulgarelis M, Ziakas PD. Images in clinical medicine. Renal papillary necrosis unmasking sickle cell disease. N Engl J Med. Mar 24 2005;352(12):1237. [Medline].

  39. Wen SF. Nephrotoxicities of nonsteroidal anti-inflammatory drugs. J Formos Med Assoc. Mar 1997;96(3):157-71. [Medline].

  40. Zadeii G, Lohr JW. Renal papillary necrosis in a patient with sickle cell trait. J Am Soc Nephrol. Jun 1997;8(6):1034-9. [Medline].

Further Reading

Keywords

papillary necrosis, renal papillary necrosis, RPN, renal medullary necrosis, medullary necrosis, interstitial nephritis, sloughed papilla, urinary obstruction, ureteropelvic junction obstruction, UPJ obstruction, ureteral obstruction, ureterovesical junction obstruction, analgesic nephropathy, analgesic-induced nephropathy, analgesic abuse, pyelonephritis, tubulointerstitial nephritis, urinary tract infection, UTI, sickle cell hemoglobinopathy, sickle cell trait, sickle cell disease, tuberculosis, cirrhosis of the liver, cirrhosis, chronic alcoholism, renal transplant rejection, diabetes mellitus, diabetes complications, systemic vasculitis, phenacetin

Contributor Information and Disclosures

Author

Jeffrey M Donohoe, MD, Assistant Professor of Pediatric Urology, Department of Surgery, Division of Urology, Medical College of Georgia
Jeffrey M Donohoe, MD is a member of the following medical societies: American Academy of Pediatrics and American Urological Association
Disclosure: Nothing to disclose.

Coauthor(s)

Jack H Mydlo, MD, Chief, Department of Urology, Woodhull Hospital; Chair and Professor, Department of Urology, Temple University School of Medicine
Jack H Mydlo, MD is a member of the following medical societies: American College of Surgeons, American Urological Association, International College of Surgeons US Section, and Society of University Urologists
Disclosure: Nothing to disclose.

Medical Editor

Gamal Mostafa Ghoniem, MD, FACS, Fellowship Program Director, Clinical Professor of Surgery, Head, Section of Voiding Dysfunction, Female Urology and Reconstruction, Cleveland Clinic Florida
Gamal Mostafa Ghoniem, MD, FACS is a member of the following medical societies: American College of Surgeons, American Urological Association, Society for Urology and Engineering, and Society of University Urologists
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

CME Editor

J Stuart Wolf, Jr, MD, FACS, David A Bloom Professor of Urology, Director, Division of Minimally Invasive Urology, Department of Urology, University of Michigan Medical Center
J Stuart Wolf, Jr, MD, FACS is a member of the following medical societies: American College of Surgeons, American Medical Association, American Urological Association, Catholic Medical Association, Endourological Society, Society for Urology and Engineering, Society of Laparoendoscopic Surgeons, and Society of University Urologists
Disclosure: Terumo Corporation Consulting fee Consulting; Omeros Corporation Consulting fee Consulting

Chief Editor

Bradley Fields Schwartz, DO, FACS, Associate Professor of Urology, Director, Center for Laparoscopy and Endourology, Department of Surgery, Southern Illinois University School of Medicine
Bradley Fields Schwartz, DO, FACS is a member of the following medical societies: American College of Surgeons, American Urological Association, Association of Military Osteopathic Physicians and Surgeons, Endourological Society, Society of Laparoendoscopic Surgeons, and Society of University Urologists
Disclosure: Nothing to disclose.

 
 
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