Nanni Lorenzo, Buonuomo Valentina, Gessi Marco, Lauriola Libero, Pintus Claudio
Department of Pediatrics, Division of Pediatric Surgery, Università Cattolica del Sacro Cuore, Policlinico A. Gemelli, Roma, Italy.
Arch Ital Urol Androl. 2005 Dec;77(4):199-201.
A case of cystic dysplasia of the rete testis (CDRT) is reported. Nine months after right orchidopexy, a 10-year-old boy presented a palpable mass in the ipsilateral hemi-scrotum. Preoperative ultrasound showed a cystic lesion involving almost the whole testis. Radical orchidectomy was performed and at gross examination a hilar multiloculated cystic lesion was confirmed; microscopic examination showed cystic spaces lined by benign appearing monostratified epithelium with atrophy of the surrounding testicular parenchyma. These findings were consistent with the diagnosis of cystic dysplasia of the rete testis. Immunohistochemical investigation evidenced a pattern similar to that of a normal rete testis. Renal ultrasound and DTPA scintigraphy performed after pathological diagnosis documented the absence of the ipsilateral kidney. CDRT is a rare cause of scrotal swelling in the pediatric patient. When diagnosis is suspected, based on clinical and sonographic findings, conservative surgery may be considered.
本文报告一例睾丸网囊性发育异常(CDRT)病例。一名10岁男孩在右侧睾丸固定术9个月后,同侧半阴囊出现可触及的肿块。术前超声显示一个几乎累及整个睾丸的囊性病变。行根治性睾丸切除术,大体检查证实为 hilar 多房囊性病变;显微镜检查显示囊性腔隙内衬良性单层上皮,周围睾丸实质萎缩。这些发现符合睾丸网囊性发育异常的诊断。免疫组织化学研究显示其模式与正常睾丸网相似。病理诊断后进行的肾脏超声和二巯基丁二酸(DTPA)闪烁扫描显示同侧肾脏缺如。CDRT 是小儿患者阴囊肿胀的罕见原因。当根据临床和超声检查结果怀疑诊断时,可考虑保守手术。