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已发表论文
阴道副神经节瘤：一个病例报导与文献综述
Authors Cai T, Li YC, Jiang QM, Wang D, Huang Y
Published Date June 2014 Volume 2014:7 Pages 965—968
DOI http://dx.doi.org/10.2147/OTT.S62174
Received 10 February 2014, Accepted 6 April 2014, Published 10 June 2014
Abstract: Vaginal paraganglioma is a rare and unusual tumor occurring in the vaginal wall. It is a solitary primary paraganglioma, especially in atypical sites. Herein, we report an unusual case of a 17-year-old woman who had not experienced vomiting, or hypertension. She was found to have an immobile solid mass in the right side of her vaginal wall. Positron emission tomography/computed tomography scans revealed a well-defined solid ovoid mass adjacent to the bladder and pelvic floor. Tumor markers were within the normal range. A transient blood pressure increase occurred during the biopsy. After oral administration of antihypertensive drugs, surgery was performed to completely remove the mass. Histopathological examination indicated that it was a paraganglioma of the vagina. Repeat computed tomography examination did not reveal any local recurrence or distant metastasis during the 12-month follow-up period.
Keywords: vaginal paraganglioma, neuroendocrine tumor, clinical features, treatment
