Pheochromocytoma in a pregnant woman.

F. H. Liu*, B. R. Hsu, J. S. Tsai

*此作品的通信作者

研究成果: 期刊稿件文章同行評審

4 引文 斯高帕斯(Scopus)

摘要

Pheochromocytoma is a rare cause of hypertension. It is even more unusual when associated with gestation. We report a 24-year-old housewife who developed episodic palpitations, flushed face and hypertension during the early postpartum period. Her symptoms were usually induced by abdominal palpation. Biochemical studies, anatomic localization with computed tomography and 131I-metaiodobenzylguanidine scan identified an adrenal tumor in the left adrenal gland. The patient underwent a left adrenalectomy without any complications. Pathologic examination of the tissue confirmed the clinical diagnosis of pheochromocytoma.

原文英語
頁(從 - 到)333-336
頁數4
期刊Journal of the Formosan Medical Association
95
發行號4
出版狀態已出版 - 04 1996
對外發佈

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