肾上腺外嗜铬细胞瘤伴严重血尿及排尿后头痛，一种罕见膀胱肿瘤实体的病例报告
Extraadrenal pheochromocytoma presenting with severe hematuria and postmicturition cephalgia, a case report of a rare bladder tumor entity.
作者信息
Sonderer Julian, Krull Ina, Schmid Hans-Peter, Müllhaupt Gautier
机构信息
Department of Urology, Institute for Medicine, University St.Gallen, Rorschacher Strasse 95, 9000, St.Gallen, Switzerland.
Department of Endocrinology, Institute for Medicine, University St.Gallen, Rorschacher Strasse 95, 9000, St.Gallen, Switzerland.
出版信息
Urol Case Rep. 2022 Jul 18;44:102170. doi: 10.1016/j.eucr.2022.102170. eCollection 2022 Sep.
Paraganglioma (PGL) of the urinary bladder are a very rare tumor entity. Treatment of a PGL requires a multidisciplinary approach. We report on a case of a malignant pheochromocytoma (PHEO) of the bladder in a male adult due to a succinate dehydrogenase B (SDHB) subunit gene mutation where a partial cystectomy was perfomed after preoperative alpha blocking.
膀胱副神经节瘤（PGL）是一种非常罕见的肿瘤类型。PGL的治疗需要多学科方法。我们报告一例成年男性因琥珀酸脱氢酶B（SDHB）亚基基因突变导致的膀胱恶性嗜铬细胞瘤（PHEO）病例，该患者在术前进行α受体阻滞剂治疗后接受了部分膀胱切除术。
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