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Erschienen in: Pediatric Nephrology 2/2009

01.02.2009 | Review

Management and etiology of the unilateral multicystic dysplastic kidney: a review

verfasst von: David S. Hains, Carlton M. Bates, Susan Ingraham, Andrew L. Schwaderer

Erschienen in: Pediatric Nephrology | Ausgabe 2/2009

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Abstract

In children, unilateral multicystic dysplastic kidney (MCDK) is one of the most frequently identified urinary tract abnormalities. A variety of proposed etiologies has been associated with the underlying pathogenesis of MCDK. These include genetic disturbances, teratogens, in utero infections, and urinary outflow tract obstruction. From 5–43% of the time, MCDK has associated genito-urinary anomalies, both structural and functional in nature. A review of the literature reveals that involution rates are reported to be 19–73%, compensatory hypertrophy of the contralateral kidney occurs from 24–81% of the time, and estimated glomerular filtration rates (GFRs) (by the Schwartz formula) range from 86–122 ml/min per 1.73 m2 body surface area. Most authors suggest serial ultrasonography to monitor contralateral growth, routine blood pressure monitoring, and a serum creatinine monitoring algorithm. The risk of hypertension in those with MCDKs does not appear to be greater than that of the general population, and the rates of malignant transformation of MCDK are small, if at all increased, in comparison with those in the general population. If the patient develops a urinary tract infection or has abnormalities of the contralateral kidney, shown on ultrasound, a voiding cystourethrogram is recommended. Finally, the body of literature does not support the routine surgical removal of MCDKs.
Literatur
1.
Zurück zum Zitat Feldenberg LR, Siegel NJ (2000) Clinical course and outcome for children with multicystic dysplastic kidneys. Pediatr Nephrol 14:1098–1101PubMed Feldenberg LR, Siegel NJ (2000) Clinical course and outcome for children with multicystic dysplastic kidneys. Pediatr Nephrol 14:1098–1101PubMed
2.
Zurück zum Zitat James CA, Watson AR, Twining P, Rance CH (1998) Antenatally detected urinary tract abnormalities: changing incidence and management. Eur J Pediatr 157:508–511PubMed James CA, Watson AR, Twining P, Rance CH (1998) Antenatally detected urinary tract abnormalities: changing incidence and management. Eur J Pediatr 157:508–511PubMed
3.
Zurück zum Zitat Kohaut EC, Tejani A (1996) The 1994 annual report of the North American Pediatric Renal Transplant Cooperative Study. Pediatr Nephrol 10:422–434CrossRefPubMed Kohaut EC, Tejani A (1996) The 1994 annual report of the North American Pediatric Renal Transplant Cooperative Study. Pediatr Nephrol 10:422–434CrossRefPubMed
4.
Zurück zum Zitat Rudnik-Schoneborn S, John U, Deget F, Ehrich JH, Misselwitz J, Zerres K (1998) Clinical features of unilateral multicystic renal dysplasia in children. Eur J Pediatr 157:666–672PubMed Rudnik-Schoneborn S, John U, Deget F, Ehrich JH, Misselwitz J, Zerres K (1998) Clinical features of unilateral multicystic renal dysplasia in children. Eur J Pediatr 157:666–672PubMed
5.
Zurück zum Zitat Mackie GG, Stephens FD (1975) Duplex kidneys: a correlation of renal dysplasia with position of the ureteral orifice. J Urol 114:274–280PubMed Mackie GG, Stephens FD (1975) Duplex kidneys: a correlation of renal dysplasia with position of the ureteral orifice. J Urol 114:274–280PubMed
6.
Zurück zum Zitat Batourina E, Tsai S, Lambert S, Sprenkle P, Viana R, Dutta S, Hensle T, Wang F, Niederreither K, McMahon AP, Carroll TJ, Mendelsohn CL (2005) Apoptosis induced by vitamin A signaling is crucial for connecting the ureters to the bladder. Nat Genet 37:1082–1089PubMed Batourina E, Tsai S, Lambert S, Sprenkle P, Viana R, Dutta S, Hensle T, Wang F, Niederreither K, McMahon AP, Carroll TJ, Mendelsohn CL (2005) Apoptosis induced by vitamin A signaling is crucial for connecting the ureters to the bladder. Nat Genet 37:1082–1089PubMed
7.
Zurück zum Zitat Viana R, Batourina E, Huang H, Dressler GR, Kobayashi A, Behringer RR, Shapiro E, Hensle T, Lambert S, Mendelsohn C (2007) The development of the bladder trigone, the center of the anti-reflux mechanism. Development 134:3763–3769PubMed Viana R, Batourina E, Huang H, Dressler GR, Kobayashi A, Behringer RR, Shapiro E, Hensle T, Lambert S, Mendelsohn C (2007) The development of the bladder trigone, the center of the anti-reflux mechanism. Development 134:3763–3769PubMed
8.
Zurück zum Zitat Belk RA, Thomas DF, Mueller RF, Godbole P, Markham AF, Weston MJ (2002) A family study and the natural history of prenatally detected unilateral multicystic dysplastic kidney. J Urol 167:666–669PubMed Belk RA, Thomas DF, Mueller RF, Godbole P, Markham AF, Weston MJ (2002) A family study and the natural history of prenatally detected unilateral multicystic dysplastic kidney. J Urol 167:666–669PubMed
9.
Zurück zum Zitat Konig R, Fuchs S, Dukiet C (1994) Branchio-oto-renal (BOR) syndrome: variable expressivity in a five-generation pedigree. Eur J Pediatr 153:446–450PubMed Konig R, Fuchs S, Dukiet C (1994) Branchio-oto-renal (BOR) syndrome: variable expressivity in a five-generation pedigree. Eur J Pediatr 153:446–450PubMed
10.
Zurück zum Zitat Murer L, Benetti E, Artifoni L (2007) Embryology and genetics of primary vesico-ureteric reflux and associated renal dysplasia. Pediatr Nephrol 22:788–797PubMedPubMedCentral Murer L, Benetti E, Artifoni L (2007) Embryology and genetics of primary vesico-ureteric reflux and associated renal dysplasia. Pediatr Nephrol 22:788–797PubMedPubMedCentral
11.
Zurück zum Zitat Murawski IJ, Gupta IR (2006) Vesicoureteric reflux and renal malformations: a developmental problem. Clin Genet 69:105–117PubMed Murawski IJ, Gupta IR (2006) Vesicoureteric reflux and renal malformations: a developmental problem. Clin Genet 69:105–117PubMed
12.
Zurück zum Zitat Murawski IJ, Myburgh DB, Favor J, Gupta IR (2007) Vesico-ureteric reflux and urinary tract development in the Pax2 1Neu+/- mouse. Am J Physiol Renal Physiol 293:F1736–F1745PubMed Murawski IJ, Myburgh DB, Favor J, Gupta IR (2007) Vesico-ureteric reflux and urinary tract development in the Pax2 1Neu+/- mouse. Am J Physiol Renal Physiol 293:F1736–F1745PubMed
13.
Zurück zum Zitat Fletcher J, Hu M, Berman Y, Collins F, Grigg J, McIver M, Juppner H, Alexander SI (2005) Multicystic dysplastic kidney and variable phenotype in a family with a novel deletion mutation of PAX2. J Am Soc Nephrol 16:2754–2761PubMed Fletcher J, Hu M, Berman Y, Collins F, Grigg J, McIver M, Juppner H, Alexander SI (2005) Multicystic dysplastic kidney and variable phenotype in a family with a novel deletion mutation of PAX2. J Am Soc Nephrol 16:2754–2761PubMed
14.
Zurück zum Zitat Petrikovsky BM, Lipson SM, Kaplan MH (2003) Viral studies on amniotic fluid from fetuses with and without abnormalities detected by prenatal sonography. J Reprod Med 48:230–232PubMed Petrikovsky BM, Lipson SM, Kaplan MH (2003) Viral studies on amniotic fluid from fetuses with and without abnormalities detected by prenatal sonography. J Reprod Med 48:230–232PubMed
15.
Zurück zum Zitat Chan M, Hecht JL, Boyd T, Rosen S (2007) Congenital cytomegalovirus infection: a cause of renal dysplasia? Pediatr Dev Pathol 10:300–304PubMed Chan M, Hecht JL, Boyd T, Rosen S (2007) Congenital cytomegalovirus infection: a cause of renal dysplasia? Pediatr Dev Pathol 10:300–304PubMed
16.
Zurück zum Zitat Carta M, Cimador M, Giuffre M, Sergio M, Di Pace MR, De Grazia E, Corsello G (2007) Unilateral multicystic dysplastic kidney in infants exposed to antiepileptic drugs during pregnancy. Pediatr Nephrol 22:1054–1057PubMed Carta M, Cimador M, Giuffre M, Sergio M, Di Pace MR, De Grazia E, Corsello G (2007) Unilateral multicystic dysplastic kidney in infants exposed to antiepileptic drugs during pregnancy. Pediatr Nephrol 22:1054–1057PubMed
18.
Zurück zum Zitat Peters CA, Carr MC, Lais A, Retik AB, Mandell J (1992) The response of the fetal kidney to obstruction. J Urol 148:503–509PubMed Peters CA, Carr MC, Lais A, Retik AB, Mandell J (1992) The response of the fetal kidney to obstruction. J Urol 148:503–509PubMed
19.
Zurück zum Zitat Shibata S, Nagata M (2003) Pathogenesis of human renal dysplasia: an alternative scenario to the major theories. Pediatr Int 45:605–609PubMed Shibata S, Nagata M (2003) Pathogenesis of human renal dysplasia: an alternative scenario to the major theories. Pediatr Int 45:605–609PubMed
20.
Zurück zum Zitat Miyazaki Y, Ichikawa I (2003) Ontogeny of congenital anomalies of the kidney and urinary tract, CAKUT. Pediatr Int 45:598–604PubMed Miyazaki Y, Ichikawa I (2003) Ontogeny of congenital anomalies of the kidney and urinary tract, CAKUT. Pediatr Int 45:598–604PubMed
21.
Zurück zum Zitat Aslam M, Watson AR (2006) Unilateral multicystic dysplastic kidney: long term outcomes. Arch Dis Child 91:820–823PubMedPubMedCentral Aslam M, Watson AR (2006) Unilateral multicystic dysplastic kidney: long term outcomes. Arch Dis Child 91:820–823PubMedPubMedCentral
22.
Zurück zum Zitat Wacksman J, Phipps L (1993) Report of the Multicystic Kidney Registry: preliminary findings. J Urol 150:1870–1872PubMed Wacksman J, Phipps L (1993) Report of the Multicystic Kidney Registry: preliminary findings. J Urol 150:1870–1872PubMed
23.
Zurück zum Zitat Kaneyama K, Yamataka A, Satake S, Yanai T, Lane GJ, Kaneko K, Yamashiro Y, Miyano T (2004) Associated urologic anomalies in children with solitary kidney. J Pediatr Surg 39:85–87PubMed Kaneyama K, Yamataka A, Satake S, Yanai T, Lane GJ, Kaneko K, Yamashiro Y, Miyano T (2004) Associated urologic anomalies in children with solitary kidney. J Pediatr Surg 39:85–87PubMed
24.
Zurück zum Zitat Kessler OJ, Ziv N, Livne PM, Merlob P (1998) Involution rate of multicystic renal dysplasia. Pediatrics 102:E73PubMed Kessler OJ, Ziv N, Livne PM, Merlob P (1998) Involution rate of multicystic renal dysplasia. Pediatrics 102:E73PubMed
25.
Zurück zum Zitat Kuwertz-Broeking E, Brinkmann OA, Von Lengerke HJ, Sciuk J, Fruend S, Bulla M, Harms E, Hertle L (2004) Unilateral multicystic dysplastic kidney: experience in children. BJU Int 93:388–392PubMed Kuwertz-Broeking E, Brinkmann OA, Von Lengerke HJ, Sciuk J, Fruend S, Bulla M, Harms E, Hertle L (2004) Unilateral multicystic dysplastic kidney: experience in children. BJU Int 93:388–392PubMed
26.
Zurück zum Zitat Menster M, Mahan J, Koff S (1994) Multicystic dysplastic kidney. Pediatr Nephrol 8:113–115PubMed Menster M, Mahan J, Koff S (1994) Multicystic dysplastic kidney. Pediatr Nephrol 8:113–115PubMed
27.
Zurück zum Zitat Miller DC, Rumohr JA, Dunn RL, Bloom DA, Park JM (2004) What is the fate of the refluxing contralateral kidney in children with multicystic dysplastic kidney? J Urol 172:1630–1634PubMed Miller DC, Rumohr JA, Dunn RL, Bloom DA, Park JM (2004) What is the fate of the refluxing contralateral kidney in children with multicystic dysplastic kidney? J Urol 172:1630–1634PubMed
28.
Zurück zum Zitat Onal B, Kogan BA (2006) Natural history of patients with multicystic dysplastic kidney—what followup is needed? J Urol 176:1607–1611PubMed Onal B, Kogan BA (2006) Natural history of patients with multicystic dysplastic kidney—what followup is needed? J Urol 176:1607–1611PubMed
29.
Zurück zum Zitat Rahman RC, Amoreo O (2005) Multicystic dysplastic kidney: diagnosis and evolution. Pediatr Nephrol 20:1023PubMed Rahman RC, Amoreo O (2005) Multicystic dysplastic kidney: diagnosis and evolution. Pediatr Nephrol 20:1023PubMed
30.
Zurück zum Zitat John U, Rudnik-Schoneborn S, Zerres K, Misselwitz J (1998) Kidney growth and renal function in unilateral multicystic dysplastic kidney disease. Pediatr Nephrol 12:567–571PubMed John U, Rudnik-Schoneborn S, Zerres K, Misselwitz J (1998) Kidney growth and renal function in unilateral multicystic dysplastic kidney disease. Pediatr Nephrol 12:567–571PubMed
31.
Zurück zum Zitat Merrot T, Lumenta DB, Tercier S, Morisson-Lacombes G, Guys JM, Alessandrini P (2006) Multicystic dysplastic kidney with ipsilateral abnormalities of genitourinary tract: experience in children. Urology 67:603–607PubMed Merrot T, Lumenta DB, Tercier S, Morisson-Lacombes G, Guys JM, Alessandrini P (2006) Multicystic dysplastic kidney with ipsilateral abnormalities of genitourinary tract: experience in children. Urology 67:603–607PubMed
32.
Zurück zum Zitat Rabelo EA, Oliveira EA, Diniz JS, Silva JM, Filgueiras MT, Pezzuti IL, Tatsuo ES (2004) Natural history of multicystic kidney conservatively managed: a prospective study. Pediatr Nephrol 19:1102–1107PubMed Rabelo EA, Oliveira EA, Diniz JS, Silva JM, Filgueiras MT, Pezzuti IL, Tatsuo ES (2004) Natural history of multicystic kidney conservatively managed: a prospective study. Pediatr Nephrol 19:1102–1107PubMed
33.
Zurück zum Zitat Rabelo EA, Oliveira EA, Silva GS, Pezzuti IL, Tatsuo ES (2005) Predictive factors of ultrasonographic involution of prenatally detected multicystic dysplastic kidney. BJU Int 95:868–871PubMed Rabelo EA, Oliveira EA, Silva GS, Pezzuti IL, Tatsuo ES (2005) Predictive factors of ultrasonographic involution of prenatally detected multicystic dysplastic kidney. BJU Int 95:868–871PubMed
34.
Zurück zum Zitat Siqueira Rabelo EA, Oliveira EA, Silva JM, Oliveira DS, Colosimo EA (2006) Ultrasound progression of prenatally detected multicystic dysplastic kidney. Urology 68:1098–1102PubMed Siqueira Rabelo EA, Oliveira EA, Silva JM, Oliveira DS, Colosimo EA (2006) Ultrasound progression of prenatally detected multicystic dysplastic kidney. Urology 68:1098–1102PubMed
35.
Zurück zum Zitat Ylinen E, Ahonen S, Ala-Houhala M, Wikstrom S (2004) Nephrectomy for multicystic dysplastic kidney: if and when? Urology 63:768–771; discussion 771–762PubMed Ylinen E, Ahonen S, Ala-Houhala M, Wikstrom S (2004) Nephrectomy for multicystic dysplastic kidney: if and when? Urology 63:768–771; discussion 771–762PubMed
36.
Zurück zum Zitat Abidari JM, Park KH, Kennedy WA, Shortliffe LD (2002) Serial followup of the contralateral renal size in children with multicystic dysplastic kidney. J Urol 168:1821–1825 discussion 1825PubMed Abidari JM, Park KH, Kennedy WA, Shortliffe LD (2002) Serial followup of the contralateral renal size in children with multicystic dysplastic kidney. J Urol 168:1821–1825 discussion 1825PubMed
38.
Zurück zum Zitat Mei-Zahav M, Korzets Z, Cohen I, Kessler O, Rathaus V, Wolach B, Pomeranz A (2001) Ambulatory blood pressure monitoring in children with a solitary kidney—a comparison between unilateral renal agenesis and uninephrectomy. Blood Press Monit 6:263–267PubMed Mei-Zahav M, Korzets Z, Cohen I, Kessler O, Rathaus V, Wolach B, Pomeranz A (2001) Ambulatory blood pressure monitoring in children with a solitary kidney—a comparison between unilateral renal agenesis and uninephrectomy. Blood Press Monit 6:263–267PubMed
39.
Zurück zum Zitat Wikstad I, Celsi G, Larsson L, Herin P, Aperia A (1988) Kidney function in adults born with unilateral renal agenesis or nephrectomized in childhood. Pediatr Nephrol 2:177–182PubMed Wikstad I, Celsi G, Larsson L, Herin P, Aperia A (1988) Kidney function in adults born with unilateral renal agenesis or nephrectomized in childhood. Pediatr Nephrol 2:177–182PubMed
40.
Zurück zum Zitat Konda R, Sato H, Ito S, Sakai K, Kimura N, Nagura H (2001) Renin containing cells are present predominantly in scarred areas but not in dysplastic regions in multicystic dysplastic kidney. J Urol 166:1910–1914PubMed Konda R, Sato H, Ito S, Sakai K, Kimura N, Nagura H (2001) Renin containing cells are present predominantly in scarred areas but not in dysplastic regions in multicystic dysplastic kidney. J Urol 166:1910–1914PubMed
41.
Zurück zum Zitat Oliveira EA, Silva AC, Rabelo EA, Filgueiras FF, Pereira AK, Mesquita FM (2002) Spontaneous improvement of hypertension in multicystic dysplastic kidney: a case report. Pediatr Nephrol 17:954–958PubMed Oliveira EA, Silva AC, Rabelo EA, Filgueiras FF, Pereira AK, Mesquita FM (2002) Spontaneous improvement of hypertension in multicystic dysplastic kidney: a case report. Pediatr Nephrol 17:954–958PubMed
42.
Zurück zum Zitat Javadpour N, Chelouhy E, Moncada L, Rosenthal IM, Bush IM (1970) Hypertension in a child caused by a multicystic kidney. J Urol 104:918–921PubMed Javadpour N, Chelouhy E, Moncada L, Rosenthal IM, Bush IM (1970) Hypertension in a child caused by a multicystic kidney. J Urol 104:918–921PubMed
43.
Zurück zum Zitat Angermeier KW, Kay R, Levin H (1992) Hypertension as a complication of multicystic dysplastic kidney. Urology 39:55–58PubMed Angermeier KW, Kay R, Levin H (1992) Hypertension as a complication of multicystic dysplastic kidney. Urology 39:55–58PubMed
44.
Zurück zum Zitat Chen YH, Stapleton FB, Roy S 3rd, Noe HN (1985) Neonatal hypertension from a unilateral multicystic dysplastic kidney. J Urol 133:664–665PubMed Chen YH, Stapleton FB, Roy S 3rd, Noe HN (1985) Neonatal hypertension from a unilateral multicystic dysplastic kidney. J Urol 133:664–665PubMed
45.
Zurück zum Zitat Husmann DA (1998) Renal dysplasia: the risks and consequences of leaving dysplastic tissue in situ. Urology 52:533–536PubMed Husmann DA (1998) Renal dysplasia: the risks and consequences of leaving dysplastic tissue in situ. Urology 52:533–536PubMed
46.
Zurück zum Zitat Snodgrass WT (2000) Hypertension associated with multicystic dysplastic kidney in children. J Urol 164:472–473; discussion 473–474PubMed Snodgrass WT (2000) Hypertension associated with multicystic dysplastic kidney in children. J Urol 164:472–473; discussion 473–474PubMed
47.
Zurück zum Zitat Pardo de la Vega R, Herrero Morin D, Ordonez Alvarez FA, Martinez Suarez V, Santos Rodriguez F, Malaga Guerrero S (2003) Ambulatory blood pressure monitoring in multicystic dysplastic kidney disease. An Pediatr (Barc) 58:545–549 Pardo de la Vega R, Herrero Morin D, Ordonez Alvarez FA, Martinez Suarez V, Santos Rodriguez F, Malaga Guerrero S (2003) Ambulatory blood pressure monitoring in multicystic dysplastic kidney disease. An Pediatr (Barc) 58:545–549
48.
Zurück zum Zitat Narchi H (2005) Risk of hypertension with multicystic kidney disease: a systematic review. Arch Dis Child 90:921–924PubMedPubMedCentral Narchi H (2005) Risk of hypertension with multicystic kidney disease: a systematic review. Arch Dis Child 90:921–924PubMedPubMedCentral
49.
Zurück zum Zitat Selzman AA, Elder JS (1995) Contralateral vesicoureteral reflux in children with a multicystic kidney. J Urol 153:1252–1254PubMed Selzman AA, Elder JS (1995) Contralateral vesicoureteral reflux in children with a multicystic kidney. J Urol 153:1252–1254PubMed
50.
Zurück zum Zitat Birken G, King D, Vane D, Lloyd T (1985) Renal cell carcinoma arising in a multicystic dysplastic kidney. J Pediatr Surg 20:619–621PubMed Birken G, King D, Vane D, Lloyd T (1985) Renal cell carcinoma arising in a multicystic dysplastic kidney. J Pediatr Surg 20:619–621PubMed
51.
Zurück zum Zitat Hartman GE, Smolik LM, Shochat SJ (1986) The dilemma of the multicystic dysplastic kidney. Am J Dis Child 140:925–928PubMed Hartman GE, Smolik LM, Shochat SJ (1986) The dilemma of the multicystic dysplastic kidney. Am J Dis Child 140:925–928PubMed
52.
Zurück zum Zitat Webb NJ, Lewis MA, Bruce J, Gough DC, Ladusans EJ, Thomson AP, Postlethwaite RJ (1997) Unilateral multicystic dysplastic kidney: the case for nephrectomy. Arch Dis Child 76:31–34PubMedPubMedCentral Webb NJ, Lewis MA, Bruce J, Gough DC, Ladusans EJ, Thomson AP, Postlethwaite RJ (1997) Unilateral multicystic dysplastic kidney: the case for nephrectomy. Arch Dis Child 76:31–34PubMedPubMedCentral
53.
Zurück zum Zitat Homsy YL, Anderson JH, Oudjhane K, Russo P (1997) Wilms tumor and multicystic dysplastic kidney disease. J Urol 158:2256–2259; discussion 2259–2260PubMed Homsy YL, Anderson JH, Oudjhane K, Russo P (1997) Wilms tumor and multicystic dysplastic kidney disease. J Urol 158:2256–2259; discussion 2259–2260PubMed
54.
Zurück zum Zitat Narchi H (2005) Risk of Wilms’ tumour with multicystic kidney disease: a systematic review. Arch Dis Child 90:147–149PubMedPubMedCentral Narchi H (2005) Risk of Wilms’ tumour with multicystic kidney disease: a systematic review. Arch Dis Child 90:147–149PubMedPubMedCentral
55.
Zurück zum Zitat Cambio AJ, Evans CP, Kurzrock EA (2008) Non-surgical management of multicystic dysplastic kidney. BJU Int 101:804–808PubMed Cambio AJ, Evans CP, Kurzrock EA (2008) Non-surgical management of multicystic dysplastic kidney. BJU Int 101:804–808PubMed
56.
Zurück zum Zitat Mingin GC, Gilhooly P, Sadeghi-Nejad H (2000) Transitional cell carcinoma in a multicystic dysplastic kidney. J Urol 163:544PubMed Mingin GC, Gilhooly P, Sadeghi-Nejad H (2000) Transitional cell carcinoma in a multicystic dysplastic kidney. J Urol 163:544PubMed
57.
Zurück zum Zitat Rackley RR, Angermeier KW, Levin H, Pontes JE, Kay R (1994) Renal cell carcinoma arising in a regressed multicystic dysplastic kidney. J Urol 152:1543–1545PubMed Rackley RR, Angermeier KW, Levin H, Pontes JE, Kay R (1994) Renal cell carcinoma arising in a regressed multicystic dysplastic kidney. J Urol 152:1543–1545PubMed
58.
Zurück zum Zitat Oliveira EA, Diniz JS, Vilasboas AS, Rabelo EA, Silva JM, Filgueiras MT (2001) Multicystic dysplastic kidney detected by fetal sonography: conservative management and follow-up. Pediatr Surg Int 17:54–57PubMed Oliveira EA, Diniz JS, Vilasboas AS, Rabelo EA, Silva JM, Filgueiras MT (2001) Multicystic dysplastic kidney detected by fetal sonography: conservative management and follow-up. Pediatr Surg Int 17:54–57PubMed
59.
Zurück zum Zitat van Eijk L, Cohen-Overbeek TE, den Hollander NS, Nijman JM, Wladimiroff JW (2002) Unilateral multicystic dysplastic kidney: a combined pre- and postnatal assessment. Ultrasound Obstet Gynecol 19:180–183PubMed van Eijk L, Cohen-Overbeek TE, den Hollander NS, Nijman JM, Wladimiroff JW (2002) Unilateral multicystic dysplastic kidney: a combined pre- and postnatal assessment. Ultrasound Obstet Gynecol 19:180–183PubMed
60.
Zurück zum Zitat Avni FE, Garel L, Cassart M, Massez A, Eurin D, Didier F, Hall M, Teele RL (2006) Perinatal assessment of hereditary cystic renal diseases: the contribution of sonography. Pediatr Radiol 36:405–414PubMed Avni FE, Garel L, Cassart M, Massez A, Eurin D, Didier F, Hall M, Teele RL (2006) Perinatal assessment of hereditary cystic renal diseases: the contribution of sonography. Pediatr Radiol 36:405–414PubMed
61.
Zurück zum Zitat Singh I, Sharma D, Singh N, Jain BK, Minocha VR (2002) Hydronephrotic obstructed kidney mimicking a congenital multicystic kidney: case report with review of literature. Int Urol Nephrol 34:179–182PubMed Singh I, Sharma D, Singh N, Jain BK, Minocha VR (2002) Hydronephrotic obstructed kidney mimicking a congenital multicystic kidney: case report with review of literature. Int Urol Nephrol 34:179–182PubMed
62.
Zurück zum Zitat Woodward M, Frank D (2002) Postnatal management of antenatal hydronephrosis. BJU Int 89:149–156PubMed Woodward M, Frank D (2002) Postnatal management of antenatal hydronephrosis. BJU Int 89:149–156PubMed
63.
Zurück zum Zitat Choyke PL, Siegel MJ, Craft AW, Green DM, DeBaun MR (1999) Screening for Wilms tumor in children with Beckwith-Wiedemann syndrome or idiopathic hemihypertrophy. Med Pediatr Oncol 32:196–200PubMed Choyke PL, Siegel MJ, Craft AW, Green DM, DeBaun MR (1999) Screening for Wilms tumor in children with Beckwith-Wiedemann syndrome or idiopathic hemihypertrophy. Med Pediatr Oncol 32:196–200PubMed
64.
Zurück zum Zitat Ismaili K, Avni FE, Alexander M, Schulman C, Collier F, Hall M (2005) Routine voiding cystourethrography is of no value in neonates with unilateral multicystic dysplastic kidney. J Pediatr 146:759–763PubMed Ismaili K, Avni FE, Alexander M, Schulman C, Collier F, Hall M (2005) Routine voiding cystourethrography is of no value in neonates with unilateral multicystic dysplastic kidney. J Pediatr 146:759–763PubMed
65.
Zurück zum Zitat Flack CE, Bellinger MF (1993) The multicystic dysplastic kidney and contralateral vesicoureteral reflux: protection of the solitary kidney. J Urol 150:1873–1874PubMed Flack CE, Bellinger MF (1993) The multicystic dysplastic kidney and contralateral vesicoureteral reflux: protection of the solitary kidney. J Urol 150:1873–1874PubMed
66.
Zurück zum Zitat McMann LP, Kirsch AJ, Scherz HC, Smith EA, Jones RA, Shehata BM, Kozielski R, Grattan-Smith JD (2006) Magnetic resonance urography in the evaluation of prenatally diagnosed hydronephrosis and renal dysgenesis. J Urol 176:1786–1792PubMed McMann LP, Kirsch AJ, Scherz HC, Smith EA, Jones RA, Shehata BM, Kozielski R, Grattan-Smith JD (2006) Magnetic resonance urography in the evaluation of prenatally diagnosed hydronephrosis and renal dysgenesis. J Urol 176:1786–1792PubMed
67.
Zurück zum Zitat Rodriguez LV, Spielman D, Herfkens RJ, Shortliffe LD (2001) Magnetic resonance imaging for the evaluation of hydronephrosis, reflux and renal scarring in children. J Urol 166:1023–1027PubMed Rodriguez LV, Spielman D, Herfkens RJ, Shortliffe LD (2001) Magnetic resonance imaging for the evaluation of hydronephrosis, reflux and renal scarring in children. J Urol 166:1023–1027PubMed
68.
Zurück zum Zitat National High Blood Pressure Education Program Working Group on High Blood Pressure in Children and Adolescents (2004) The fourth report on the diagnosis, evaluation, and treatment of high blood pressure in children and adolescents. Pediatrics 114:555–576 National High Blood Pressure Education Program Working Group on High Blood Pressure in Children and Adolescents (2004) The fourth report on the diagnosis, evaluation, and treatment of high blood pressure in children and adolescents. Pediatrics 114:555–576
69.
Zurück zum Zitat Kaneko K, Yamashiro Y, Yamataka A, Miyano T (2005) Nephrectomy for multicystic dysplastic kidneys: a new therapeutic option. Pediatr Nephrol 20:690–691PubMed Kaneko K, Yamashiro Y, Yamataka A, Miyano T (2005) Nephrectomy for multicystic dysplastic kidneys: a new therapeutic option. Pediatr Nephrol 20:690–691PubMed
70.
Zurück zum Zitat Steven LC, Li AG, Driver CP, Mahomed AA (2005) Laparoscopic nephrectomy for unilateral multicystic dysplastic kidney in children. Surg Endosc 19:1135–1138PubMed Steven LC, Li AG, Driver CP, Mahomed AA (2005) Laparoscopic nephrectomy for unilateral multicystic dysplastic kidney in children. Surg Endosc 19:1135–1138PubMed
Metadaten
Titel
Management and etiology of the unilateral multicystic dysplastic kidney: a review
verfasst von
David S. Hains
Carlton M. Bates
Susan Ingraham
Andrew L. Schwaderer
Publikationsdatum
01.02.2009
Verlag
Springer Berlin Heidelberg
Erschienen in
Pediatric Nephrology / Ausgabe 2/2009
Print ISSN: 0931-041X
Elektronische ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-008-0828-8

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