Pseudopapillary Granulosa Cell Tumor: A Case of This Rare Subtype

Conclusion. The pseudopapillary pattern of granulosa cell tumor is rare and must be suspected in order to utilize appropriate immunohistochemistry and reach the correct diagnosis. Inhibin positivity is particularly helpful.

Source: International Journal of Surgical Pathology - June 27, 2016 Category: Pathology Authors: Heller, D., Haddad, A., Cracchiolo, B. Tags: Pitfalls in Pathology Source Type: research