Ovarian Sex Cord Stromal Tumor, Steroid Cell, NOS in an Adolescent: A Case Report

被引:7
|
作者
Schnuckle, Emma M. [1 ]
Williamson, Amy [2 ]
Carpentieri, David [3 ]
Taylor, Steve [3 ]
机构
[1] Creighton Univ, Sch Med, Phoenix, AZ USA
[2] Phoenix Childrens Hosp, Dept Pediat & Adolescent Gynecol, Phoenix, AZ 85006 USA
[3] Phoenix Childrens Hosp, Dept Pathol, Phoenix, AZ 85006 USA
关键词
Sex cord stromal tumor; Steroid cell tumor; Virilization; Androgen; Adolescent; Salpingo-oophorectomy; Case report;
D O I
10.1016/j.jpag.2020.08.001
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Background: Ovarian steroid cell tumor, not otherwise specified (NOS), is a rare type of sex cord stromal tumor, which often presents with androgenic symptoms and has a high frequency of malignancy. Case: This is a case of a 14-year-old Native American girl who presented with acne, amenorrhea, and virilization and was found to have a 2.9-cm solid ovarian mass. Initial pathology revealed steroid-appearing cells with round nuclei, clear/vacuolated cytoplasm, and a low mitotic index. Final diagnosis was ovarian steroid cell tumor, NOS Stage IA. A laparoscopic left salpingo-oophorectomy was subsequently performed. No tumor recurrence was noted 2 years after her initial diagnosis. Summary and Conclusion: Long-term data on these tumors are limited; however, malignancy, recurrence, and death have been reported. This suggests that close follow-up is essential for appropriate management.
引用
收藏
页码:94 / 97
页数:4
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