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Composite Paraganglioma and Neuroblastoma of the Urinary Bladder: A Rare Histopathological Entity

机译:膀胱的复合伞菌和神经母细胞瘤:罕见的组织病理实体

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摘要

Paraganglioma of the urinary bladder is an uncommon clinical entity. Neuroblastoma of the urinary bladder is another rare tumor with only 7 reported cases, all in children. This report presents the case of a composite paraganglioma and neuroblastoma in a 45 year-old male who presented with dysuria and flank pain. On the computerized tomography scan, the bladder wall overlying the tumor was smooth and the mass had a large exophytic component. The initial diagnosis was paraganglioma on transurethral resection. Following partial cystectomy and bilateral pelvic lymph node dissection, pathology confirmed a composite tumor consisting of paraganglioma and neuroblastoma. To our knowledge, this is the first report of such a composite tumor involving the bladder.
机译:膀胱膀胱囊肿是一种罕见的临床实体。 膀胱的神经母细胞瘤是另一个罕见的肿瘤,只有7例患者,所有人都在儿童中。 本报告呈现了一个患有困扰和侧翼疼痛的45岁男性中复合伞菌性和神经母细胞瘤的情况。 在电脑断层扫描扫描上,覆盖肿瘤的膀胱壁是光滑的,并且质量具有大的突出组分。 初始诊断是经尿道切除术的伞菌。 在部分膀胱切除术和双侧骨盆淋巴结解剖后,病理学证实了一种由Paraganglioma和神经母细胞瘤组成的复合肿瘤。 据我们所知,这是第一份涉及膀胱的复合肿瘤的报告。

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