首页> 外文期刊>International journal of urology: official journal of the Japanese Urological Association >Spontaneous rupture of adrenal pheochromocytoma with capsular invasion.
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Spontaneous rupture of adrenal pheochromocytoma with capsular invasion.

机译:肾上腺嗜铬细胞瘤自发破裂伴包膜浸润。

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Abstract A 67-year-old Japanese man developed a sudden onset of severe right-side upper abdominal pain, nausea and vomiting. On hospitalization, physical examination revealed sweating, tachycardia, hypertension and the appearance of peripheral vasoconstriction. An urgent computed tomography scan with contrast demonstrated a large hematoma in the right retroperitoneal space. A phentolamine test and an (131)iodine metaiodobenzylguanidine scan suggested pheochromocytoma. An elective right adrenalectomy was successfully performed after pretreatment for sufficient volume replacement with continuous administration of alpha- and beta-adrenergic blocking agents. Pathological diagnosis was an adrenal pheochromocytoma 9.0 x 6.5 cm in diameter with evidence of capsular invasion, which could be associated with a tear in the capsule.
机译:摘要一名67岁的日本男子突然发作严重的右侧上腹部疼痛,恶心和呕吐。住院时,体格检查发现出汗,心动过速,高血压和周围血管收缩的出现。紧急计算​​机断层扫描(对比)显示右腹膜后间隙有较大的血肿。苯酚胺试验和(131)碘间碘苄基胍扫描提示嗜铬细胞瘤。预处理后,通过连续施用α-和β-肾上腺素能阻断剂,成功进行了选择性右肾上腺切除术,以进行足够的体积置换。病理诊断为直径9.0 x 6.5 cm的肾上腺嗜铬细胞瘤,有荚膜浸润的迹象,这可能与囊膜撕裂有关。

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