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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

Zinner’s Syndrome: A Confusing Diagnosis in the Face of Chronic Disabling Perineoscrotal Pain in the Young Subject, about a Case
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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 Z<span style="white-space:nowrap;">&iuml;</span>nner 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. 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 Z<span style="white-space:nowrap;">&iuml;</span>nner 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.
作者 Ntambwe Nkashama Jean-Louis Mouhssine Errehan Kwizera Juvenal Mamoutou Mody Keita Lakmichi Mohamed Amine Dahami Zakaria Moudouni Mohamed Sarf Ismail Ntambwe Nkashama Jean-Louis;Mouhssine Errehan;Kwizera Juvenal;Mamoutou Mody Keita;Lakmichi Mohamed Amine;Dahami Zakaria;Moudouni Mohamed;Sarf Ismail(Service d’Urologie, Chu Mohamed Vi De Marrakech, Marrakech, Maroc)
机构地区 Service d’Urologie
出处 《Case Reports in Clinical Medicine》 2021年第5期141-145,共5页 临床医学病理报告(英文)
关键词 AGENESIS Congenital Malformation KIDNEY Perineoscrotal Pain Seminal Vesicles Zinner’s Syndrome Agenesis Congenital Malformation Kidney Perineoscrotal Pain Seminal Vesicles Zinner’s Syndrome
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