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2.
Eur J Pediatr ; 173(12): 1623-5, 2014 Dec.
Article in English | MEDLINE | ID: mdl-24213483

ABSTRACT

UNLABELLED: Renal involvement is regularly encountered in neonates with invasive candidiasis, especially when risk factors like congenital malformations of the renal tract or poor bladder emptying and preterm birth are present. However, complete obstruction of the renal collecting system by fungal balls is rare. Although conservative management has been advocated for partial obstruction, complete obstruction is considered an indication for surgical drainage. We report a patient with anuria and Candida albicans bezoars in a solitary kidney, suggesting post-renal acute kidney injury. The patient was treated with systemic fluconazole and peritoneal dialysis for 4 days. The fungus balls disappeared and renal function recovered. CONCLUSION: Systemic antifungal therapy leads to clearance of obstructing fungus balls, and nephrostomy should be reserved for anuria due to bilateral complete obstruction with severe hydronephrosis. In these cases, temporary dialysis is a potential alternative.


Subject(s)
Antifungal Agents/therapeutic use , Anuria/etiology , Bezoars/complications , Candida albicans/isolation & purification , Candidiasis/complications , Kidney/abnormalities , Renal Dialysis/methods , Anuria/diagnostic imaging , Anuria/therapy , Bezoars/diagnostic imaging , Bezoars/microbiology , Candidiasis/diagnostic imaging , Candidiasis/therapy , Diagnosis, Differential , Humans , Infant, Newborn , Kidney/diagnostic imaging , Kidney/microbiology , Male , Ultrasonography
3.
Thorax ; 65(7): 652-3, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20627926

ABSTRACT

Screening for cystic fibrosis (CF) was recently added to the neonatal screening programme in the Netherlands. Four patients with renal failure whose heel prick tests were positive for CF as defined by raised levels of immunoreactive trypsinogen (IRT) and pancreatitis-associated protein (PAP) are described. Both cystic fibrosis transmembrane conductance regulator (CFTR) DNA analysis and sweat tests were negative. Limited renal function can be a cause of false positive neonatal screening for CF using IRT and PAP.


Subject(s)
Cystic Fibrosis/diagnosis , Neonatal Screening/methods , Renal Insufficiency/blood , Antigens, Neoplasm/blood , Biomarkers/blood , Biomarkers, Tumor/blood , Cystic Fibrosis Transmembrane Conductance Regulator/genetics , False Positive Reactions , Humans , Infant, Newborn , Lectins, C-Type/blood , Male , Pancreatitis-Associated Proteins , Trypsinogen/blood
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