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Pseudopapillary Granulosa Cell Tumor: A Case of This Rare Subtype
Accepted manuscript   Open access   Peer reviewed

Pseudopapillary Granulosa Cell Tumor: A Case of This Rare Subtype

Debra Heller, Andrew Haddad and Bernadette Cracchiolo
International Journal of Surgical Pathology, Vol.24(5), pp.425-426
2016
DOI:
https://doi.org/10.7282/T3VD71P1

Abstract

Ovarian neoplasms Granulosa cell tumor Diagnosis Differential
Background: The pseudopapillary pattern of granulosa cell tumor is rare. Case:We describe a the case of a 35-year-old woman who presented with an initial diagnosis of papillary serous cystadenocarcinoma Results: Evaluation, including immunohistochemistry, led to the diagnosis of pseudopapillary granulosa cell tumor. 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.
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Accepted Manuscript (AM) Open Access
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http://dx.doi.org/10.1177/1066896916640361View
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