29.12.2021 Views

Diagnostic ultrasound ( PDFDrive )

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

CHAPTER 39 The Fetal Urogenital Tract 1373

158. Epelman M, Daneman A, Donnelly LF, et al. Neonatal imaging evaluation

of common prenatally diagnosed genitourinary abnormalities. Semin

Ultrasound CT MR. 2014;35(6):528-554.

159. Laing FC, Burke VD, Wing VW, et al. Postpartum evaluation of fetal

hydronephrosis: optimal timing for follow-up sonography. Radiology.

1984;152(2):423-424.

160. de Bruyn R, Gordon I. Postnatal investigation of fetal renal disease. Prenat

Diagn. 2001;21(11):984-991.

161. Lidefelt KJ, Ek S, Mihocsa L. Is screening for vesicoureteral relux mandatory

in infants with antenatal renal pelvis dilatation? Acta Paediatr. 2006;

95(12):1653-1656.

162. Vivier PH, Dolores M, Taylor M, et al. MR urography in children. Part 1:

how we do the F0 technique. Pediatr Radiol. 2010;40(5):732-738.

163. Vivier PH, Dolores M, Taylor M, Dacher JN. MR urography in children.

Part 2: how to use ImageJ MR urography processing sotware. Pediatr Radiol.

2010;40(5):739-746.

164. Quirino IG, Diniz JS, Bouzada MC, et al. Clinical course of 822 children

with prenatally detected nephrouropathies. Clin J Am Soc Nephrol.

2012;7(3):444-451.

165. Chevalier RL, hornhill BA, Forbes MS, Kiley SC. Mechanisms of renal

injury and progression of renal disease in congenital obstructive nephropathy.

Pediatr Nephrol. 2010;25(4):687-697.

166. Gokce I, Biyikli N, Tugtepe H, et al. Clinical spectrum of antenatally detected

urinary tract abnormalities with respect to hydronephrosis at postnatal

ultrasound scan. Pediatr Surg Int. 2012;28(5):543-552.

167. Pates JA, Dashe JS. Prenatal diagnosis and management of hydronephrosis.

Early Hum Dev. 2006;82(1):3-8.

168. Alberti C. Congenital ureteropelvic junction obstruction: physiopathology,

decoupling of tout court pelvic dilatation-obstruction semantic connection,

biomarkers to predict renal damage evolution. Eur Rev Med Pharmacol

Sci. 2012;16(2):213-219.

169. Karnak I, Woo LL, Shah SN, et al. Results of a practical protocol for management

of prenatally detected hydronephrosis due to ureteropelvic junction

obstruction. Pediatr Surg Int. 2009;25(1):61-67.

170. Gorincour G, Rypens F, Toiviainen-Salo S, et al. Fetal urinoma: two new

cases and a review of the literature. Ultrasound Obstet Gynecol. 2006;28(6):

848-852.

171. Barker AP, Cave MM, homas DF, et al. Fetal pelvi-ureteric junction

obstruction: predictors of outcome. Br J Urol. 1995;76(5):649-652.

172. Liu HY, Dhillon HK, Yeung CK, et al. Clinical outcome and management

of prenatally diagnosed primary megaureters. J Urol. 1994;152(2 Pt

2):614-617.

173. Berrocal T, Lopez-Pereira P, Arjonilla A, Gutierrez J. Anomalies of the

distal ureter, bladder, and urethra in children: embryologic, radiologic, and

pathologic features. Radiographics. 2002;22(5):1139-1164.

174. McLellan DL, Retik AB, Bauer SB, et al. Rate and predictors of spontaneous

resolution of prenatally diagnosed primary nonreluxing megaureter. J Urol.

2002;168(5):2177-2180.

175. Shukla AR, Cooper J, Patel RP, et al. Prenatally detected primary megaureter:

a role for extended followup. J Urol. 2005;173(4):1353-1356.

176. Calisti A, Oriolo L, Perrotta ML, et al. he fate of prenatally diagnosed

primary nonreluxing megaureter: do we have reliable predictors for

spontaneous resolution? Urology. 2008;72(2):309-312.

177. Whitten SM, Wilcox DT. Duplex systems. Prenat Diagn.

2001;21(11):952-957.

178. Abuhamad AZ, Horton Jr CE, Horton SH, Evans AT. Renal duplication

anomalies in the fetus: clues for prenatal diagnosis. Ultrasound Obstet

Gynecol. 1996;7(3):174-177.

179. Vergani P, Ceruti P, Locatelli A, et al. Accuracy of prenatal ultrasonographic

diagnosis of duplex renal system. J Ultrasound Med. 1999;18(7):463-467.

180. Whitten SM, McHoney M, Wilcox DT, et al. Accuracy of antenatal fetal

ultrasound in the diagnosis of duplex kidneys. Ultrasound Obstet Gynecol.

2003;21(4):342-346.

181. Adiego B, Martinez-Ten P, Perez-Pedregosa J, et al. Antenatally diagnosed

renal duplex anomalies: sonographic features and long-term postnatal

outcome. J Ultrasound Med. 2011;30(6):809-815.

182. Godinho AB, Nunes C, Janeiro M, et al. Ureterocele: antenatal diagnosis

and management. Fetal Diagn her. 2013;34(3):188-191.

183. Torres Montebruno X, Martinez JM, Eixarch E, et al. Fetoscopic laser surgery

to decompress distal urethral obstruction caused by prolapsed ureterocele.

Ultrasound Obstet Gynecol. 2015;46(5):623-626.

184. Upadhyay J, Bolduc S, Braga L, et al. Impact of prenatal diagnosis on the

morbidity associated with ureterocele management. J Urol. 2002;167(6):

2560-2565.

185. Anderson NG, Allan RB, Abbott GD. Fluctuating fetal or neonatal renal

pelvis: marker of high-grade vesicoureteral relux. Pediatr Nephrol.

2004;19(7):749-753.

186. Zerin JM, Ritchey ML, Chang AC. Incidental vesicoureteral relux in neonates

with antenatally detected hydronephrosis and other renal abnormalities.

Radiology. 1993;187(1):157-160.

187. van Eerde AM, Meutgeert MH, de Jong TP, Giltay JC. Vesico-ureteral relux

in children with prenatally detected hydronephrosis: a systematic review.

Ultrasound Obstet Gynecol. 2007;29(4):463-469.

188. Ismaili K, Avni FE, Hall M. Results of systematic voiding cystourethrography

in infants with antenatally diagnosed renal pelvis dilation. J Pediatr.

2002;141(1):21-24.

189. Ismaili K, Hall M, Piepsz A, et al. Primary vesicoureteral relux detected

in neonates with a history of fetal renal pelvis dilatation: a prospective

clinical and imaging study. J Pediatr. 2006;148(2):222-227.

190. Penido Silva JM, Oliveira EA, Diniz JS, et al. Clinical course of prenatally

detected primary vesicoureteral relux. Pediatr Nephrol. 2006;21(1):

86-91.

191. Sebire NJ, Von Kaisenberg C, Rubio C, et al. Fetal megacystis at 10-14

weeks of gestation. Ultrasound Obstet Gynecol. 1996;8(6):387-390.

192. Yiee J, Wilcox D. Abnormalities of the fetal bladder. Semin Fetal Neonatal

Med. 2008;13(3):164-170.

193. Montemarano H, Bulas DI, Rushton HG, Selby D. Bladder distention and

pyelectasis in the male fetus: causes, comparisons, and contrasts. J Ultrasound

Med. 1998;17(12):743-749.

194. Liao AW, Sebire NJ, Geerts L, et al. Megacystis at 10-14 weeks of gestation:

chromosomal defects and outcome according to bladder length. Ultrasound

Obstet Gynecol. 2003;21(4):338-341.

195. Carroll SG, Soothill PW, Tizard J, Kyle PM. Vesicocentesis at 10-14 weeks

of gestation for treatment of fetal megacystis. Ultrasound Obstet Gynecol.

2001;18(4):366-370.

196. Bernardes LS, Aksnes G, Saada J, et al. Keyhole sign: how speciic is it for

the diagnosis of posterior urethral valves? Ultrasound Obstet Gynecol.

2009;34(4):419-423.

197. Perks AE, MacNeily AE, Blair GK. Posterior urethral valves. J Pediatr Surg.

2002;37(7):1105-1107.

198. Gonzalez R, De Filippo R, Jednak R, Barthold JS. Urethral atresia: long-term

outcome in 6 children who survived the neonatal period. J Urol. 2001;165(6

Pt 2):2241-2244.

199. Papantoniou N, Papoutsis D, Daskalakis G, et al. Prenatal diagnosis of

prune-belly syndrome at 13 weeks of gestation: case report and review of

literature. J Matern Fetal Neonatal Med. 2010;23(10):1263-1267.

200. Osborne NG, Bonilla-Musoles F, Machado LE, et al. Fetal megacystis:

diferential diagnosis. J Ultrasound Med. 2011;30(6):833-841.

201. Sepulveda W, Elorza C, Gutierrez J, et al. Congenital megalourethra: outcome

ater prenatal diagnosis in a series of 4 cases. J Ultrasound Med. 2005;24(9):

1303-1308.

202. Amsalem H, Fitzgerald B, Keating S, et al. Congenital megalourethra: prenatal

diagnosis and postnatal/autopsy indings in 10 cases. Ultrasound Obstet

Gynecol. 2011;37(6):678-683.

203. Fitzsimons RB, Keohane C, Galvin J. Prune belly syndrome with ultrasound

demonstration of reduction of megacystis in utero. Br J Radiol.

1985;58(688):374-376.

204. Garel C, Dreux S, Philippe-Chomette P, et al. Contribution of fetal magnetic

resonance imaging and amniotic luid digestive enzyme assays to the

evaluation of gastrointestinal tract abnormalities. Ultrasound Obstet Gynecol.

2006;28(3):282-291.

205. Muller F, Dreux S, Vaast P, et al. Prenatal diagnosis of megacystis-microcolon–

intestinal hypoperistalsis syndrome: contribution of amniotic luid digestive

enzyme assay and fetal urinalysis. Prenat Diagn. 2005;25(3):203-209.

206. Anneren G, Meurling S, Olsen L. Megacystis-microcolon–intestinal

hypoperistalsis syndrome (MMIHS), an autosomal recessive disorder: clinical

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!