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脐尿管瘘表现为脐部脓毒症:一名成年男性的罕见病例。

Urachal fistula presenting as umbilical sepsis: a rare case in an adult male.

作者信息

Hurreiz Hisham, Hussain Irshad, Hamo Ishrak

机构信息

Newham General Hospital, Glen Road, London, UK.

出版信息

Med Sci Monit. 2006 May;12(5):CS44-7.

Abstract

BACKGROUND

Urachal anomalies are rare normally presenting during childhood. They are difficult to diagnose and surgical treatment is always needed to prevent recurrence.

CASE REPORT

A 28 year old male presented with a red tender umbilical swelling that was confused with an umbilical hernia. The correct diagnosis of a urachal fistula was reached after performing a CT scan. The patient was initially treated with oral antibiotics and complete surgical excision of the fistulous tract was carried out at a later stage after controlling the infection.

CONCLUSIONS

Staged resection is the treatment of choice in urachal anomalies associated with sepsis. Surgical excision of the urachal remnant is necessary to prevent recurrence.

摘要

背景

脐尿管异常通常在儿童期出现,较为罕见。它们难以诊断,且总是需要手术治疗以防止复发。

病例报告

一名28岁男性出现红色、触痛的脐部肿胀,曾被误诊为脐疝。经CT扫描后确诊为脐尿管瘘。患者最初接受口服抗生素治疗,在控制感染后,后期进行了瘘管的完全手术切除。

结论

分期切除是伴有败血症的脐尿管异常的首选治疗方法。切除脐尿管残余组织对于预防复发是必要的。

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