pheochromocytomas

pheochromocytomas

美 　英

• 網絡腎上腺嗜鉻細胞瘤；嗜鉻色素細胞瘤

例句

Pheochromocytomas can be asymptomatic but may cause sustained or episodic hypertension.

但也可引起持續或癥狀性高血壓。

Conclusion Multislice Spiral CT scans and MRP for diagnose pheochromocytomas have higher value.

結論多層螺旋CT掃描及MRP對嗜鉻細胞瘤的定性和定位診斷有較高價值。

Methods 18 cases by surgery and pathology adrenal pheochromocytomas imaging data were analyzed retrospectively.

方法回顧性分析經手術和病理證實18例腎上腺嗜鉻細胞瘤的患者的影像學的資料。

Only about 2% of pheochromocytomas in children are malignant but most of those are extra-adrenal.

僅約2%的幼童嗜鉻細胞瘤為惡性的，且大多數是位于腎上腺外。

Pheochromocytomas are rare tumors that occur in approximately 0. 1% of patients with hypertension.

嗜鉻細胞瘤為一罕見之腫瘤，約0.1%之高血壓病人可發現有此腫瘤。

Objective: To study the angiographic manifestations and complications in patients with adrenal pheochromocytomas.

目的：探討腎上腺嗜鉻細胞瘤的血管造影表現及并發癥。