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Cystic lymphatic malformation of bladder presenting as a pelvic mass.

机译:膀胱的囊性淋巴畸形,表现为盆腔包块。

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摘要

We report a 5-year-old boy with a cystic lymphatic malformation (LM) of bladder, and the imaging characteristics of the lesion are reported. Cystic LM of the urinary system is rare, and a location in the bladder is extremely rare. The exact mechanism of the lesion that occurs in bladder is unknown. This case is different from the 3 cases reported before, for it is only presented with a palpable pelvic mass and the lesion did not penetrate full thickness of bladder. Although imaging examinations are helpful in the definition of cystic LMs, no characteristic findings are available to diagnose a cystic LM of the bladder before surgery. The diagnosis is always made after surgical intervention. Surgical excision is ideal, and an extensive operation is not warranted because the lesion is benign. Once excised completely, the prognosis of the disease is good.
机译:我们报告了一个5岁的男孩与膀胱囊性淋巴畸形(LM),并报告了病变的影像学特征。泌尿系统的囊性LM很少见,膀胱中的位置极为罕见。膀胱中病变的确切机制尚不清楚。该病例与之前报道的3例不同,因为仅表现为可触及的骨盆肿块,且病变未穿透膀胱的整个厚度。尽管影像学检查有助于确定囊性LM,但尚无特征性发现可用于手术前诊断膀胱的囊性LM。诊断始终在手术干预后进行。手术切除是理想的,并且由于病变是良性的,因此不宜进行广泛的手术。一旦完全切除,该病的预后良好。

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