Juvenile Granulosa Cell Tumors of the Ovary.

CONCLUSIONS: JGCT is a rare neoplasm with a wide morphologic spectrum and is easily confused with other tumors. Familiarity with the characteristics, rare atypical appearances, and immunohistochemical results may aid in obtaining a correct diagnosis.
PMID: 32561911 [PubMed - as supplied by publisher]

Source: American Journal of Clinical Pathology - June 19, 2020 Category: Pathology Authors: Ye Y, Lv C, Xu S, Chen Y, Qian R, Wang P, Wang S Tags: Am J Clin Pathol Source Type: research