Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

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Gewählte Publikation:

Riccabona, M; Ring, E; Häusler, M; Ratschek, M; Fotter, R.
Neonatal segmental cystic nephroma. A case report
Z Geburtshilfe Neonatol. 1999; 203(6):255-257
Web of Science PubMed

 

Führende Autor*innen der Med Uni Graz
Riccabona Michael
Co-Autor*innen der Med Uni Graz
Fotter Richard
Haeusler Martin
Ratschek Manfred
Ring Ekkehard
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Abstract:
Multicystic segmental renal dysplasia is rare in early childhood. We report a case with prenatally recognized renal malformation. Prenatally a cystic renal malformation was detected sonographically; postnatally further evaluation was performed by Doppler sonography, contrast enhanced CT and voiding cysto-urethrography leading to the diagnosis of a multicystic segmental nephroma. Due to increasing size in spite of therapeutic and diagnostic sonographic guided punctures and the atypic manifestation the baby underwent heminephrectomy. The final histological diagnosis confirmed preoperativ findings. CONCLUSION: Prenatally recognised cystiform renal malformations should be reevaluated postpartally by ultrasound and--as doubtful findings are found--further imaging might be necessary for follow up and for the decision on conservative or operative treatment.
Find related publications in this database (using NLM MeSH Indexing)
Adult -
Diagnosis, Differential -
Female -
Humans -
Infant, Newborn -
Kidney Neoplasms - congenital
Nephrectomy - congenital
Pregnancy - congenital
Tomography, X-Ray Computed - congenital
Ultrasonography, Prenatal - congenital
Urography - congenital
Wilms Tumor - congenital

Find related publications in this database (Keywords)
sonography
segmental dysplasia
cystic renal malformation
neonates
prenatal diagnosis
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