- 期刊
- OpenAccess
Malignant Pheochromocytoma of the Adrenal Gland: a case Report and Review of the Literature
惡性嗜鉻細胞瘤：病例報告及文獻回顧
並列摘要
Pheochromocytoma is a rare urological disease. The ”classic triad” consists of headache, palpitation, and diaphoresis. Hypertension is the leading clinical manifestation. Herein, we report a 44-year-old male who was admitted with the chief complaint of knowing to have an intra-abdominal tumor in a general healthy examination. A series of studies were done which revealed: I) A huge ill-defined, central necrotic lesion occupied the left supra-renal area; 2) Vanillymandelic acid: 37.8 mg/24hrs urine. Exploratory laparotomy with adrenalectomy and nephrectomy via Chevron incision was done. The final clinic pathological diagnosis was pheochromocytoma of left adrenal gland with left kidney invasion. So far, this patient has been regularly followed at our outpatient clinic with a stable condition. The literatures were reviewed.
延伸閱讀
- 張天鈞（2004）。文獻選粹：轉移性嗜鉻細胞瘤定位的新方法。當代醫學，(363)，28-28。https://doi.org/10.29941/MT.200401.0010
- 翁錦興（2001）。兼論嗜鉻細胞瘤之實驗室診斷。中華民國內分泌暨糖尿病學會會訊，15(1)，20-22。https://doi.org/10.7101/EDA.200110.0020
- 黃天祥（1993）。嗜鉻細胞瘤的病理生理，診斷治療之新進展。中華民國內分泌暨糖尿病學會會訊，7(1)，6-8。https://www.airitilibrary.com/Article/Detail?DocID=a0000079-199310-7-1-6-8-a
- 翁錦興（2003）。論文評述─兼論嗜鉻細胞瘤患者之基因篩檢。中華民國內分泌暨糖尿病學會會訊，16(2)，16-18。https://doi.org/10.7101/EDA.200301.0016
- Lin, C. W., Kuo, H. T., Chen, P. J., Tzen, C. Y., & Lu, Y. T. (2004). 後縱膈腔內嗜鉻細胞瘤之病例報告及文獻回顧. 胸腔醫學, 19(6), 517-523. https://doi.org/10.29806/TM.200412.0013