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

机译:复合膀胱副神经节瘤和神经母细胞瘤:罕见的组织病理学实体。

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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:膀胱神经节旁瘤是罕见的临床实体。膀胱神经母细胞瘤是另一种罕见的肿瘤,仅报告了7例,均为儿童。本报告介绍了一名患有排尿困难和胁腹痛的45岁男性复合神经节旁瘤和神经母细胞瘤的病例。在计算机断层扫描中,覆盖在肿瘤上的膀胱壁是光滑的,肿块具有较大的外生成分。初步诊断为经尿道切除的神经节旁瘤。膀胱部分切除术和双侧盆腔淋巴结清扫术后,病理证实为由副神经节瘤和神经母细胞瘤组成的复合瘤。据我们所知,这是这种涉及膀胱的复合肿瘤的首次报道。

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