- 期刊
腎上腺嗜鉻細胞瘤之一病例報告
Adrenal Pheochromocytoma in a Child
摘要
13歲男孩，因發汗，頭痛及心悸住院。臨床檢查發現有持續性高血壓，尿液所含之vanilmandelic acid (VMA)，腎上腺素(epinephrine)，新腎上腺素(norepinephrine)及dopamine均有昇高，動脈血管攝影顯示右腎上方有血管性腫瘤。病人接受開刀治療，術後症狀消失，體重增加，同時尿液之磷苯二酚胺(catecholamine)也恢復正常。
關鍵字
無資料並列摘要
A 13-year old boy had the complaints of sweating, headache, palpitation and no body weight gain for two years. Physical examination revealed persistent hypertension and grade Ⅲ hypertensive retinopathy. Twenty-four hour urinary catecholamine (epinephrine, norephinephrine, dopamine) and VMA (vanilmandelic acid) secretions were increased. Selective suprarenal angiography showed a right side adrenal vascular tumor. A yellowish vascular tumor measuring 5×5×5cm in size was removed surgically with prompt relief of hypertension. It was later histologically proved to be a pheochromocytoma. The patient remained symptom free and his body weight increased 8kg in two months postoperatively.
延伸閱讀
- Huang, C. J., Lee, S. Y., Huang, J. J., Sung, J. M., Chang, K. C., & Liu, H. L. (2000). 腎上腺神經節神經瘤：一模仿嗜鉻細胞瘤之意外瘤. Acta Nephrologica, 14(3), 117-120. https://www.airitilibrary.com/Article/Detail?DocID=10131671-200007-14-3-117-120-a
- 馬鈞鼎、陳思達（2007）。腎上腺偶見腫瘤：病例報告及討論。中華民國內分泌暨糖尿病學會會刊，21(1)，11-19。https://doi.org/10.7101/ED.200710.0011
- 方俊慧、吳誠中、陳振鵬、吳天成、劉自嘉（1987）。腎上腺之髓脂瘤－病例報告。The Kaohsiung Journal of Medical Sciences，3(12)，783-787。https://doi.org/10.6452/KJMS.198712.0783
- Lin, J. T., Lee, Y. H., Jian, B. P., & Huang, J. K. (2001). 腎上腺神節細胞瘤：3病例報告. 中華民國泌尿科醫學會雜誌, 12(1), 42-45. https://doi.org/10.7024/JUAROC.200103.0042
- 林美慧（1991）。Congenital Adrenal Hyperplasia Present with precocious。慈濟醫學雜誌，3(4)，300-304。https://doi.org/10.6440/TZUCMJ.199112.0300