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Testicular Ectopia in the Anterior Abdominal Wall of a Neonate: A Rare Site of Ectopic Testis

机译:新生儿前腹壁的睾丸异位症:异位睾丸的罕见部位

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Patient: Male, 3-day Final Diagnosis: Ectopic right testis in anterior abdominal wall Symptoms: — Medication: — Clinical Procedure: Testicular ultrasound and MRI abdomen Specialty: Radiology Objective: Unusual clinical course Background: Abnormal testicular descent can either be undescended or, less commonly, ectopic. Most undescended testes complete the course of descent by the first year of life only if these remain in the normal path of descent. The deviation of the testis may occur to an ectopic location during the transinguinal phase. Of the known ectopic sites, the anterior abdominal wall is the rarest site of testicular ectopia and to our knowledge only 3 cases of this nature have been reported in the available literature to date. Case Report: This rare case of testicular ectopia occurred in a 3-day-old boy in whom the right scrotal sac was empty; on abdominal ultrasound, the right testis was found in the subcutaneous tissues of the right antero-lateral abdominal wall. These findings were confirmed on abdominal MRI, where the right testis was seen beneath the skin between the subcutaneous tissues and external oblique aponeurosis. No aponeurotic or muscular defect was appreciable under the abdominal wall. The neonate underwent orchiopexy at the age of 6 months and remained uneventful postoperatively. Conclusions: Preoperative imaging is recommended to detect and confirm the ectopic site as well as the morphology of testis, thereby increasing the chance of surveillance and preservation of an ectopic testis. Imaging can serve as preoperative road mapping to localize the exact site for surgical exploration of an ectopic testis if there is no apparent or palpable swelling over the anterior abdominal wall.
机译:患者:男性,为期3天最终诊断:前腹壁异位右睾丸症状:—药物治疗:—临床方法:睾丸超声和MRI腹部专长:放射学目的:异常的临床病程背景:睾丸后裔异常下降可以是不希望的,或者不常见的是异位。多数未下降的睾丸只有在其正常下降路径下才能在生命的第一年完成下降过程。睾丸期可能在异位发生睾丸偏离。在已知的异位部位中,前腹壁是睾丸异位的最罕见部位,据我们所知,迄今为止,现有文献中仅报道了3例这种性质的病例。病例报告:这种罕见的睾丸外翻病例发生在一个3天大的男孩中,其中右阴囊为空。在腹部超声检查中,在右前腹壁的皮下组织中发现了右睾丸。这些发现在腹部MRI上得到了证实,其中在皮下组织与外斜肌腱膜之间的皮肤下方看到了右睾丸。在腹壁下没有明显的腱膜或肌肉缺陷。新生儿在6个月大时进行了睾丸检查,术后无异常。结论:建议术前影像学检查以发现并确认异位部位以及睾丸的形态,从而增加监视和保存异位睾丸的机会。如果在前腹壁上没有明显的或可触及的肿胀,影像学可以作为术前的路测图,以定位用于外科手术探查异位睾丸的确切部位。

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