cystic dysplasia of the rete testis in an adolescent with vater association

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CLINICAL IMAGE Cystic dysplasia of the rete testis in an adolescent with VATER association Ellen Park & Stuart Morrison Received: 16 July 2007 / Revised: 20 August 2007 / Accepted: 31 August 2007 / Published online: 16 October 2007 # Springer-Verlag 2007 A 13-year-old was referred for scrotal US for painless enlargement of the right testicle. US showed multiple dilated fluid-filled spaces in the rete testis with compressed normal testicular parenchyma (Fig. 1). VATER association had been diagnosed with an absent right kidney. Cystic dysplasia of the rete testis is a rare entity with only 15 cases reported in the literature up to 2001 [1]. Congenital cystic dysplasia of the rete testis is a consequence of an early insult involving the development of the mesonephric duct. This explains the almost universal association with renal agenesis or multicystic dysplastic kidney on the same side, and also helps differentiate it from a malignant tumor. Confusion exists between congenital cystic dysplasia of the rete testis and the unrelated but similarly named incidental finding in elderly men called tubular ectasia of the mediastinum testis or ectasia of the rete testis [2]. This is often bilateral and not associated with testicular enlarge- ment or renal anomalies. References 1. Piotto L, LeQuesne GW, Gent R et al (2001) Congenital cystic dysplasia of the rete testis. Pediatr Radiol 31:724726 2. Brown D, Benson CB, Doherty FJ et al (1992) Cystic testicular mass caused by dilated rete testis: sonographic findings in 31 cases. AJR 158:12571259 Pediatr Radiol (2008) 38:123 DOI 10.1007/s00247-007-0646-3 E. Park : S. Morrison (*) Diagnostic Radiology, The Cleveland Clinic Childrens Hospital, 9500 Euclid Avenue, Cleveland, OH 44195, USA e-mail: [email protected] Fig. 1 Right testicular US

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Page 1: Cystic dysplasia of the rete testis in an adolescent with VATER association

CLINICAL IMAGE

Cystic dysplasia of the rete testis in an adolescentwith VATER association

Ellen Park & Stuart Morrison

Received: 16 July 2007 /Revised: 20 August 2007 /Accepted: 31 August 2007 / Published online: 16 October 2007# Springer-Verlag 2007

A 13-year-old was referred for scrotal US for painlessenlargement of the right testicle. US showed multipledilated fluid-filled spaces in the rete testis with compressednormal testicular parenchyma (Fig. 1). VATER associationhad been diagnosed with an absent right kidney.

Cystic dysplasia of the rete testis is a rare entity with only

15 cases reported in the literature up to 2001 [1]. Congenitalcystic dysplasia of the rete testis is a consequence of an earlyinsult involving the development of the mesonephric duct.This explains the almost universal association with renal

agenesis or multicystic dysplastic kidney on the same side,and also helps differentiate it from a malignant tumor.

Confusion exists between congenital cystic dysplasia ofthe rete testis and the unrelated but similarly namedincidental finding in elderly men called tubular ectasia ofthe mediastinum testis or ectasia of the rete testis [2]. This

is often bilateral and not associated with testicular enlarge-ment or renal anomalies.

References

1. Piotto L, LeQuesne GW, Gent R et al (2001) Congenital cysticdysplasia of the rete testis. Pediatr Radiol 31:724–726

2. Brown D, Benson CB, Doherty FJ et al (1992) Cystic testicularmass caused by dilated rete testis: sonographic findings in 31 cases.AJR 158:1257–1259

Pediatr Radiol (2008) 38:123DOI 10.1007/s00247-007-0646-3

E. Park : S. Morrison (*)Diagnostic Radiology, The Cleveland Clinic Children’s Hospital,9500 Euclid Avenue,Cleveland, OH 44195, USAe-mail: [email protected]

Fig. 1 Right testicular US