Spontaneous regression of suspected cystic dysplasia of the rete testis in three neonates

• Published in: Journal of pediatric urology 2016-12, Vol.12 (6), p.387.e1-387.e4
• Main Authors: Gelas, T, Deslandes, L. Margain, Mestrallet, G, Pracros, J.P, Mouriquand, P
• Format: Article
• Language: English
• Subjects: Cyst; Cysts - diagnosis; Cysts - therapy; Dysplasia; Humans; Infant, Newborn; Male; Pediatrics; Rete Testis; Testicular Diseases - diagnosis; Testicular Diseases - therapy; Urology
• ISSN: 1477-5131; 1873-4898
• DOI: 10.1016/j.jpurol.2016.05.032

Summary Introduction Cystic dysplasia of the rete testis (CDRT) is a rare cause of scrotal swelling during infancy. It is a benign lesion that is often associated with ipsilateral renal, ureteral or genital abnormalities. Leissring and Oppenheimer described it for the first time in 1973. Case reports Since 2006, three neonates were referred to the present institution because of a scrotal swelling related to intra-testicular cysts. Physical examination showed enlarged testicles without pain or inflammation. The ultrasound scan (USS) showed enlarged testicles related to multiple small cysts surrounded by normal parenchyma, and no other urinary abnormalities. As CDRT was suspected, a conservative strategy was proposed with repeated clinical examinations and USS. The cysts gradually regressed and disappeared in all cases, with a mean follow-up of 52 months. Discussion As reported by Jeyaratnam et al., mean age at presentation was around 6 years. The most frequently associated urinary abnormalities were renal agenesis and multicystic dysplasia of the kidney. Differential diagnosis of CDRT included single testicular cyst, epidermoid cyst, albugina cyst, teratoma, cystic lymphangioma, testicular juvenile granulosa cell tumor, cystic transformation after orchitis, or spermatic cord torsion. Ultrasonography was the method of choice for the diagnosis of CDRT and its follow-up. The USS showed multiple small cysts with normal, but compressed, surrounding testicular parenchyma. A high-frequency transducer was mandatory to exclude other causes of scrotal swelling. With the involution of the cysts, the aspect of the parenchyma could be slightly heterogeneous or confused with microlithiasis. Historically, orchidectomy was the proposed treatment. However, because of a more precise diagnosis with USS, a conservative approach has been proposed. Nonetheless, recurrence after sparing surgery was frequent, as reported by many authors. Non-surgical management was reported in selected cases, sometimes after a surgical biopsy to confirm a benign lesion. Spontaneous regression of DRT without any sequelae has been reported in six cases (see Summary Table ) but long-term follow-up in the adult population has never been published. Limitations of the present series were related to the small number of cases, the absence of follow-up beyond puberty, and the absence of biopsy to confirm the diagnosis of CDRT. Conclusion Spontaneous regression of CDRT was possible, and conservative attitud