副神經節瘤:病例報告
張朋暉1、林宜佳1,2、黃一勝1,2
新光吳火獅紀念醫院 外科部 泌尿科1
輔仁大學 醫學系2
Pheochromocytoma of Organ of Zuckerkandl: A Case Report and Literature Review
Peng-Hui Chang1, Yi-Chia Lin1,2, Chao-Yen Ho1, Te-Fu Tsai1,2, Thomas I.S. Hwang1,2
Division of Urology, Department of Surgery, Shin Kong WHS Memorial Hospital1
School of Medicine, Fu-Jen Catholic University2
 
Abstract:
Paraganglioma, also known as extra-adrenal pheochromocytoma, is a rare seen catecholamines-secreting neuroendocrine tumor. Excessive secretion of catecholamine cause nonspecific symptoms and signs such as headache, episodic sudden perspiration, and tachycardia. One of the common sites of extra-adrenal pheochromocytoma is organ of Zuckerkandl. Herein, we report a 61 years-old female who came to our hospital with occasional palpitation and hot flush. Intermittent hypertension was noted, too. A computed tomography scan with contrast showed a left infra-renal tumor with obstructive uropathy and involving organ of Zuckerkandl. Further lab study showed increased in only dopamine level. Her epinephrine and nor-epinephrine were within normal range. Robotic-assisted retroperitoneal tumor excision was done uneventfully. The pathology study proved the functional extra-adrenal paraganglioma. The patient did not experience further palpitation and hot flush after operation. Follow-up computed tomography showed no recurrence or metastasis and her dopamine level returned to normal. The literatures were reviewed and discussed.
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    TUA秘書處
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    台灣泌尿科醫學會
    建立
    2019-07-12 16:06:51
    最近修訂
    2019-07-12 16:30:58
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