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
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Riccabona Michael
- Co-Autor*innen der Med Uni Graz
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Fotter Richard
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Haeusler Martin
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Ratschek Manfred
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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)
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Adult -
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Diagnosis, Differential -
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Female -
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Humans -
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Infant, Newborn -
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Kidney Neoplasms - congenital
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Nephrectomy - congenital
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Pregnancy - congenital
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Tomography, X-Ray Computed - congenital
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Ultrasonography, Prenatal - congenital
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Urography - congenital
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Wilms Tumor - congenital
- Find related publications in this database (Keywords)
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sonography
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segmental dysplasia
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cystic renal malformation
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neonates
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prenatal diagnosis