Tazi Fadl, Ahsaini Mustapha, Khalouk Abdelhak, Mellas Soufiane, Stuurman-Wieringa Roos E, Elfassi Mohammed Jamal, Farih My Hassan
Department of Urology, Hospital University Center Hassan II, Fez, 30000 Morocco.
J Med Case Rep. 2012 Jul 30;6:226. doi: 10.1186/1752-1947-6-226.
Urachal diseases are rare and may develop from a congenital anomaly in which a persistent or partial reopening of the fetal communication between the bladder and the umbilicus persists. The most frequently reported urachal anomalies in adults are infected urachal cyst and urachal carcinoma. The diagnosis of this entity is not always easy because of the rarity of these diseases and the atypical symptoms at presentation. Imaging techniques, such as ultrasonography and computed tomography have a significant role in recognizing the presence of urachus-derived lesions.
Case presentation 1: A 25-year-old Arab-Berber man presented with a 10-day history of progressive lower abdominal pain accompanied by fever, vomiting, and low urinary tract symptoms to our emergency department. Laboratory data revealed leucocytosis. The diagnosis of an acute peritonitis was made initially. Abdominal ultrasonography revealed a hypoechoic tract from the umbilicus to the abdominal wall, and the diagnosis was rectified (infected urachal remnants). The patient was initially treated with intravenous antibiotics in combination with a percutaneous drainage. Afterwards an extraperitoneal excision of the urachal remnant including a cuff of bladder was performed. The histological analysis did not reveal a tumor of the urachal remnant. Follow-up examinations a few months later showed no abnormality.Case presentation 2: A 35-year-old Arab-Berber man, without prior medical history with one week of abdominal pain, nausea and vomiting, associated with fever but without lower urinary tract symptoms visited our emergency department. Laboratory data revealed leucocytosis. Abdominal ultrasonography was not conclusive. Computed tomography of the abdomen was the key to the investigation and the diagnosis of an abscess of urachal remnants was made. The patient underwent the same choice of medical-surgical treatment as previously described for case one, with a good follow-up result.Case presentation 3: A 22-year-old Arab-Berber man, with no relevant past medical history, presented to our emergency department because of suspected acute surgical abdomen. Physical examination revealed umbilical discharge with erythema and a tender umbilical mass. Abdominal ultrasonography and computed tomography scan confirmed the diagnosis of infected urachal sinus. Initial management was intravenous antibiotics associated with a percutaneous drainage with a good post-operative result, but a few days later, he was readmitted with the same complaint and the decision was made for surgical treatment consisting of excision of the infected urachal sinus. The clinical course was uneventful. Histological examination did not reveal any signs of malignancy.
We describe our clinical observations and an analysis of the existing literature to present the various clinical, radiological, pathological and therapeutic aspects of an abscess of urachal remnants. To the best of our knowledge, this manuscript is an original case report because this atypical presentation is rarely reported in the literature and only a few cases have been described.
脐尿管疾病较为罕见,可能源于先天性异常,即胎儿膀胱与脐之间的通道持续或部分重新开放。成人中最常报告的脐尿管异常是感染性脐尿管囊肿和脐尿管癌。由于这些疾病罕见且临床表现不典型,该实体的诊断并不总是容易的。超声和计算机断层扫描等成像技术在识别脐尿管源性病变的存在方面具有重要作用。
病例1:一名25岁的阿拉伯-柏柏尔族男性因进行性下腹痛10天,伴有发热、呕吐和下尿路症状,就诊于我院急诊科。实验室检查显示白细胞增多。最初诊断为急性腹膜炎。腹部超声显示从脐到腹壁的低回声通道,诊断得以纠正(感染性脐尿管残余物)。患者最初接受静脉抗生素联合经皮引流治疗。之后,对脐尿管残余物进行了包括膀胱袖口的腹膜外切除。组织学分析未发现脐尿管残余物肿瘤。几个月后的随访检查未发现异常。病例2:一名35岁的阿拉伯-柏柏尔族男性,无既往病史,因腹痛、恶心和呕吐1周,伴有发热但无下尿路症状,就诊于我院急诊科。实验室检查显示白细胞增多。腹部超声检查结果不明确。腹部计算机断层扫描是诊断的关键,诊断为脐尿管残余物脓肿。该患者接受了与病例1相同的内科-外科治疗选择,随访结果良好。病例3:一名22岁的阿拉伯-柏柏尔族男性,无相关既往病史,因疑似急性急腹症就诊于我院急诊科。体格检查发现脐部有分泌物、红斑和压痛性脐部肿块。腹部超声和计算机断层扫描证实诊断为感染性脐尿管窦。初始治疗为静脉抗生素联合经皮引流,术后效果良好,但几天后,他因同样的症状再次入院,决定进行手术治疗,切除感染性脐尿管窦。临床过程顺利。组织学检查未发现任何恶性迹象。
我们描述了我们的临床观察以及对现有文献的分析,以呈现脐尿管残余物脓肿的各种临床、放射学、病理学和治疗方面。据我们所知,本手稿是一份原始病例报告,因为这种非典型表现很少在文献中报道,仅描述了少数病例。