Coincidence of juvenile granulosa cell tumor and serous cystadenoma in a pediatric patient: Case report and literature review

Radiology Case Reports

Nguyen Minh Duc, MD,MSc¹  Le Hong Chien, MD²  Le Anh Viet, MD²  Hoang-Van Lan Duc, MD²  Dang Quang Hung, MD²  Nguyen-Thi Mai Anh, MD²  Hoang-Thi Kim Khuyen, MD²  Nguyen Hong Hai, MD²  Luu-Thi Bich Ngoc, MD² 

[1] Department of Radiology, Children's Hospital 2, Ho Chi Minh City, Vietnam;Department of Radiology, Vinmec Healthcare System, Ha Noi, Vietnam;

关键词: Granulosa cell tumor;    Juvenile granulosa cell tumor;    Ovarian serous cystadenoma;    Different bilateral ovarian tumors;   

DOI  :  

来源: DOAJ

【 摘 要 】

Juvenile granulosa cell tumor (GCT) is a rare ovarian tumor in children, presenting with a multiloculated cystic pattern and irregular wall-thickening on imaging and serous cystadenoma (SCA) is also another rare benign cystic ovarian tumor in children. The appearance of two uncommon types of ovarian tumors on both sides in children is extremely rare. We report the case of a 4-year-old female presenting with symptoms of precocious puberty and diagnosed with juvenile GCT on the left ovary after surgical resection. However, during follow-up 1 year after GCT resection, she presented with another multiloculated cystic mass in the right ovary, and diagnosed as SCA after surgical resection and histopathologic evaluations. The appearance of cystic ovarian tumor after primarily GCT resection need to differentiate between the recurrence of the primarily GCT and other cystic ovarian tumors although it is very uncommon. Furthermore, the imaging features played a key role in the differential diagnosis between benign and malignant ovarian tumors.

【 授权许可】

Unknown