Pregled bibliografske jedinice broj: 728215
The role of kidney biopsy in diagnosis of renal parenchymal anomalies in children
The role of kidney biopsy in diagnosis of renal parenchymal anomalies in children // Meeting abstract / Danica Batinić, Danko Milošević (ur.).
New York (NY): Springer, 2011. str. 1694-1695 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 728215 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
The role of kidney biopsy in diagnosis of renal parenchymal anomalies in children
Autori
Milosevic, Danko ; Batinic, Danica ; Scukanec-Spoljar, Mira ; Nizic, Ljiljana ; Vrljicak, Kristina
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Meeting abstract
/ Danica Batinić, Danko Milošević - New York (NY) : Springer, 2011, 1694-1695
Skup
Pediatrics, Urology & Nephrology
Mjesto i datum
Dubrovnik, Hrvatska, 14.09.2011. - 17.09.2011
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
kidney biopsy; renal anomalies; children
Sažetak
Objectives and study: Congenital renal parencyhimal anomalies belong in a group of rare kidney diseases associated with the end stage renal failure. Usually presented on ultrasound as “small kidneys”, the diseases assume considerable diagnostic and care workup. We analysed the percentage of renal parenchymal anomalies among kidney biopsies in our population and importance of childen/parents life style recommendations.Methods: A retrospective clinical analysis of kidney biopsies.Results: During past 13 years we peformed 450 kidney biopsies at University Hospital Centre Zagreb and Rijeka in children aged 0–17 years (22.3% of both hospital kidney biopsies, adult patients included). Congenital kidney parenchymal anomalies were diagnosed in 15 children (3.3%). Nephronophtisis was found in 8 children (median age 8.8 years, infants 1/8), oligomeganephronia revealed in 7 (median age 5.6 years, infants 5/7), of whom one child has combined histological picture of oligomeganephonia/interstitial nephritis. All children suffered eventually from progressive renal faulure. In one family we suspect of hereditary type disease. Multiple anomalies can be found in children with both diseases, primarily in oligomeganephronia.Conclusions: Early correct diagnosis enabled us to postpone end stage renal failure by children/parents life style consulting and parental genetic counselling for the future progeny.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Zagreb,
Klinički bolnički centar Zagreb
Profili:
Mira Šćukanec-Špoljar
(autor)
Kristina Vrljičak
(autor)
Danica Batinić
(autor)
Danko Milošević
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE