Juvenile granulosa cell tumor in pregnancy: case series and literature review

被引:0
作者
Ndhlovu, Elijah [1 ]
Deng, Hui [2 ]
Dai, Jun [1 ]
Dong, Xiyuan [1 ]
Liu, Lili [3 ]
Chen, Biao [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Hosp, Dept Obstet & Gynecol, Tongji Med Coll, Wuhan 430030, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Hosp, Dept Pathol, Tongji Med Coll, Wuhan 430030, Peoples R China
[3] Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Wuhan Maternal & Child Healthcare Hosp, Dept Pathol,Tongji Med Coll, Wuhan 430016, Peoples R China
关键词
Juvenile granulosa cell tumor; Pregnancy ovarian tumor; Ovarian cancer; CORD-STROMAL TUMORS; OVARIAN-CANCER; SERUM INHIBIN; PROGESTERONE; MANAGEMENT; MALIGNANCIES; CARCINOMA; APOPTOSIS; PROLIFERATION; EXPRESSION;
D O I
10.1007/s00404-021-06283-5
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Background Pregnancy complicated with juvenile granulosa cell tumor (JGCT) is very rare; thus, the experience on clinical diagnosis and management is limited. Cases Two patients presented with abdominal pain, two were incidentally discovered, one by ultrasonography, and one during a caesarian section. One case received an emergency caesarian section because of tumor rupture at 38th week's gestation, the rest were treated at full term and no abnormalities were detected in the newborns. Three cases received further staging surgery, two of which received postoperative adjuvant chemotherapy. No patient had recurrent disease after a follow-up period spanning from 13 to 57 months. Conclusion In the absence of emergency, surgery can be delayed without affecting the fetus. More research is needed to determine the value of chemotherapy in FIGO stage I patients.
引用
收藏
页码:1299 / 1310
页数:12
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