AJR AJR-based Continuing Ed for Technologists
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Figures Only
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kabaalioglu, A.
Right arrow Articles by Boneval, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kabaalioglu, A.
Right arrow Articles by Boneval, C.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?
Hotlight (NEW!)
Right arrow
What's Hotlight?
AJR 2001; 176:511-512
© American Roentgen Ray Society


Case Report

Renal Candidiasis in a 2-Month-Old Infant

Treatment of Fungus Balls with Streptokinase

Adnan Kabaaliolu1, Elif Bahat2 and Cem Boneval3

1 Department of Radiology, Akdeniz University Medical Faculty, Arapsuyu, Antalya, 07070 Turkey.
2 Department of Pediatric Nephrology, Akdeniz University Medical Faculty, Arapsuyu, Antalya, 07070 Turkey.
3 Department of Pediatric Surgery, Akdeniz University Medical Faculty, Arapsuyu, Antalya, 07070 Turkey.

Received May 12, 2000; accepted after revision August 7, 2000.

 
Address correspondence to A. Kabaaliolu.


Introduction
Top
Introduction
Case Report
Discussion
References
 
Renal candidiasis is a severe infection of the urinary tract. Premature infants, patients who are immunocompromised, and patients with diabetes are especially at increased risk for the disease. Central venous access, broad-spectrum antibiotics, and total parenteral nutrition are also risk factors for candidemia [1, 2]. Treatment may begin with parenteral antifungal agents such as fluconazole, amphotericin B, or amphotericin B combined with flucytosine. Partial or complete urinary obstruction by fungus balls is not rare during treatment [1,2,3]. Although performing nephrostomy with or without irrigation using several antifungal agents may relieve the obstruction, fungus balls may be drug-resistant and may cause renal failure [1,2,3].

We report the case of a premature infant in whom refractory fungus balls in the urinary system were cleared by streptokinase that was infused through ureteral catheters.


Case Report
Top
Introduction
Case Report
Discussion
References
 
A 2-month-old premature male infant with irritability and hypoactivity was admitted to the pediatric intensive care unit. He was born during the 26th gestational week and weighed 1120 g at birth. He had a history of respiratory distress and sepsis in the first 3 weeks of life. The infant weighed 1250 g and was in a relatively good condition when discharged from the hospital. During follow-up his development had been normal.

At admission, a physical examination revealed loss of newborn reflexes and bilateral large palpable kidneys. Remarkable laboratory findings were as follows: blood urea nitrogen level, 62 mg/dL; serum creatinine level, 3.24 mg/dL; renal failure index, 6.8; elevated level of C-reactive protein; and leukocytosis. Urinalysis showed candiduria. Sonography showed bilateral renal enlargement and echogenic foci with slight posterior acoustic shadowing in the dilated collecting systems (Fig. 1A). In addition, perirenal and peritoneal fluid that probably reflected urinary ascites was noted.



View larger version (86K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 1A. 2-month-old premature male infant with renal candidiasis. L = left, R = right. Longitudinal sonograms show bilateral dilated calices filled with echogenic debris (arrows), which reflects fungus balls.

 

Candida albicans was isolated from blood, urine, cerebrospinal fluid, and peritoneal fluid. With the diagnosis of Candida sepsis and renal candidiasis, amphotericin B was started at the dose of 1 mg/kg per day. The patient's renal function deteriorated gradually; therefore, bilateral nephrostomy tubes were placed on the eighth day of treatment and parenteral fluconazole (Triflucan; Pfizer, Istanbul, Turkey) was added. Local irrigation of the tubes with amphotericin B (Ambisome; Nexstar, Helsinn Birex, Ireland) was also started. However, the patient's general condition and sonographic findings did not improve after 10 days of drainage and irrigation by renal and perirenal catheters. Because the amount of fluid drained by the catheters decreased to less than 20 mL/day, percutaneous drainage catheters were removed.

Surgery and other alternative treatments were discussed by the official council composed of pediatric nephrologists, pediatric surgeons, urologists, and radiologists. On the basis of previous experience with percutaneous treatment of septate organized empyemas, the radiologists' suggestion to use streptokinase to lyse the thick organized fungus balls was accepted because open surgery in this patient was considered contraindicated given the condition of his kidneys. Consent from the patient's parents was also obtained. Five milliliters of streptokinase (Kabikinase; Pharmacia & Upjohn, Stockholm, Sweden) at a concentration of 3000 IU/mL was given as a bolus twice daily through transvesically implanted bilateral ureteral catheters that were extended to the renal pelvis. The ureteral catheters were then clamped for 1 hr. Thus, a total amount of 30,000 IU per day streptokinase was initially administered to each renal collecting system. The dose was selected empirically on the basis of the doses used for other interventions, the capacity of a premature infant's renal collecting system, and possibility of hemorrhagic complications. The previous systemic treatment was also maintained.

Four hours after the first dose of streptokinase, sonography showed significant improvement in the left kidney and total disappearance of the fungus balls in the right kidney (Fig. 1B). Because no complications related to treatment with streptokinase were observed, this treatment was continued for 3 days. After 10 days, clinical and sonographic findings were normal, blood urea nitrogen and creatinine levels had also returned to normal values, and the patient was sent home.



View larger version (73K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 1B. 2-month-old premature male infant with renal candidiasis. L = left, R = right. Sonograms obtained 4 hr after treatment with streptokinase show collecting systems of both kidneys to be clear of fungus balls, although mild to moderate dilatation can still be seen.

 


Discussion
Top
Introduction
Case Report
Discussion
References
 
Fungus balls in the urinary tract may cause long-lasting obstruction and renal failure despite the appropriate antifungal agents being given parenterally or via nephrostomy [1,2,3]. Surgery to remove the fungus balls is rarely necessary. In our case, the infant did not respond to the medical treatment, so surgery was considered. However, because the patient was a poor surgical candidate, a final effort was made by administering streptokinase, which is well known for its fibrinolytic effect. In a recent study, streptokinase or urokinase was used to lyse the thrombi in subclavian or jugular catheters [4], which are believed to act as sites of fungal growth. The success of urokinase in preventing Candida infections that develop in venous catheters might, at least partly, be related to the lytic effect of the drug against fungus balls, although the authors concluded that urokinase was indirectly effective [4]. Urokinase and streptokinase have also been reported to be helpful in treating thick multiseptate empyemas by breaking down the fibrin septa [5].

The exact mechanism of action for streptokinase in lysing the fungus balls in our patient is not clear. However, fibrin may adhere to long-standing fungus balls and cause them to become firmer complexes. Therefore, by lysing the fibrin in or around the fungus balls, streptokinase may facilitate their dissolution. To our knowledge, neither streptokinase nor urokinase has been previously used to lyse fungus balls. Further experimental studies are needed to fully explain the pathways of the streptokinase for its effect against fungus balls.

In conclusion, percutaneous streptokinase injection to renal pelvis through catheters, in conjunction with parenteral antifungal agents, may lyse urinary fungus balls that are resistant to medical treatment and percutaneous drainage or irrigation.


References
Top
Introduction
Case Report
Discussion
References
 

  1. Benjamin DK Jr, Fischer RG, McKinney RE Jr, Benjamin DK. Candidal mycetoma in the neonatal kidney. Pediatrics 1999;104:1126 -1129[Abstract/Free Full Text]
  2. Yoo SY, Namkoong MK. Acute renal failure caused by fungal bezoar: a late complication of Candida sepsis associated with central catheterization. J Pediatr Surg 1995;30:1600 -1602[Medline]
  3. Visser D, Monnens L, Feitz W, Semmekrot B. Fungal bezoars as a cause of renal insufficiency in neonates and infants: recommended treatment strategy. Clin Nephrol 1998;49:198 -201[Medline]
  4. Jones GR, Konsler GK, Dunaway RP, Lacey SR, Azziakhan RG. Prospective analysis of urokinase in the treatment of catheter sepsis in pediatric hematology-oncology patients. J Pediatr Surg 1993;28:350 -357[Medline]
  5. Moulton JJ, Moore PT, Mencini RA. Treatment of loculated pleural effusions with transcatheter intracavitary urokinase. AJR 1989;153:941 -945[Abstract/Free Full Text]

Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
ImagingHome page
S Mackenzie
Controversies in the radiological investigation of paediatric urinary tract infection
Imaging, December 1, 2001; 13(4): 285 - 294.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Figures Only
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kabaalioglu, A.
Right arrow Articles by Boneval, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kabaalioglu, A.
Right arrow Articles by Boneval, C.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?
Hotlight (NEW!)
Right arrow
What's Hotlight?


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS