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Chinese Journal of Medical Ultrasound (Electronic Edition) ›› 2021, Vol. 18 ›› Issue (10): 985-990. doi: 10.3877/cma.j.issn.1672-6448.2021.10.015

• Pediatric Ultrasound • Previous Articles     Next Articles

Ultrasonographic features and pathological comparison of juvenile ovary granulose cell tumors

Huan Xiao1, Yi Tang1, qiao Wang1, Lirong Zhu1, Yang Gao1, Juan Xu1, Chunjiang Yang1,()   

  1. 1. Department of Ultrasound, Children's Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Pediatrics in Chongqing, National Clinical Research Center for Child Health and Disease (Chongqing), Chongqing Key Laboratory of Pediatrics, Chongqing International Science and Technology Cooperation Center for Child Development and Disorders, Chongqing 400014, China
  • Received:2021-02-26 Online:2021-10-01 Published:2021-11-02
  • Contact: Chunjiang Yang

Abstract:

Objective

To investigate the ultrasonographic and pathological features of juvenile granulosa cell tumors (JGCTs) of the ovary in children.

Methods

The clinical data and ultrasonographic findings of 14 children with JGCTs diagnosed by surgical pathology at Children's Hospital of Chongqing Medical University from January 2005 to December 2020 were retrospectively analyzed. The ultrasonographic images of the tumors were pattern classified according to the International Ovarian Tumor Analysis Organization (IOTA) standards, and compared with the histopathological results.

Results

Fourteen patients with JGCTs were included in this study. The maximum tumor diameter range of the 14 patients was 37~286 mm, and the mean standard deviation was (105±56) mm. According to IOTA standards, the ultrasonographic manifestations of tumor were classed into five types, namely, solid (6, 42.9%), multilocular cystic solid (4, 28.6%), multilocular cystic solid (2, 14.3%), single-locular cystic solid (1, 7.1%), and single-locular cystic (1, 7.1%). The pathological results showed that the solid mass consisted of diffuse proliferation of a large number of granulosa cells with scattered follicles of unequal size, necrosis and bleeding, and fibrous cord tissue. Multilocular cystic solid, single locular cystic solid, multiple locular cystic, and single locular cystic masses had varying numbers of large follicles, most of which had basophilic and/or eosinophilic fluid secreted by granulosa cells. Clinical endocrine manifestations included breast enlargement in five cases (35.7%), and vaginal bleeding and secretion in five cases (35.7%). Ultrasound revealed uterine enlargement in ten cases (71.4%), and vaginal bleeding and secretion in five cases (35.7%). The preoperative serum estradiol level was increased in all the children, with an average of (534.0±839.5) pmol/L.

Conclusion

The ultrasonic manifestations of JGCTs are diverse, and the mixed type of solid and multilocular cystic solid lesion is more common. The pathological characteristics of JGCTs are diffuse proliferation of large granular cells with scattered follicles of different sizes. The combination of ultrasonographic features, endocrine clinical manifestations, and serum estradiol elevation is helpful for clinical diagnosis.

Key words: Granulosa cell tumor, Ovary, Ultrasonography, Histopathology, Child

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