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Zinner’s Syndrome: A Confusing Diagnosis in the Face of Chronic Disabling Perineoscrotal Pain in the Young Subject, about a Case

机译:Zinner的综合征:面对年轻对象的慢性残疾患者的慢性致病症令人困惑的综合征

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摘要

Zinner syndrome is a rare congenital malformation related to an abnormality in the development of the Wolffian duct, the clinical picture of which consists of a triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and obstruction of the ejaculatory duct. Chronic perineoscrotal pain may be an indication of the diagnosis of Zïnner syndrome to some extent. We report the observation of a 23-year-old patient, married and father of one child, who presented with chronic perineo-scrotal pain revealing on morphological assessment (ultrasound, uroscanner, prostatic MRI) a cystic formation of the seminal vesicle, left renal agenesis with an empty left renal compartment. Given the patient’s refusal of any surgical procedure, treatment consisted of echo-guided puncture of the seminal vesicle cyst bringing back 30 cc of a seroviscous liquid whose analysis revealed spermatozoa, without atypical cells, compatible with a cyst. The clinical evolution was marked by a progressive remission of the scrotal pain with a delay of several months.
机译:Zinner综合征是一种罕见的先天性畸形,与德国管道发展的异常有关,临床图象由三合一体的单侧肾功能衰退,同侧精囊囊肿和肠梗阻阻塞组成。慢性PerineoScrotal疼痛可能是Zïnner综合征在一定程度上诊断的指示。我们举报了观察一名儿童23岁的患者,已婚和父亲,他介绍了在形态评估(超声,尿道,前列腺MRI)的囊性形成的血清囊泡的囊性形成,左肾脏呈现出慢性Perineo-Clottal疼痛患有空左肾隔室的刺激。鉴于患者拒绝任何外科手术,治疗组成,由半粒子囊泡的半囊泡囊肿的回声引导穿刺,其分析显示出细胞膜,没有非典型细胞,与囊肿相容。临床演变是由阴囊疼痛的渐进式缓解,延迟几个月。

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