Objectives
This study aimed to evaluate and compare the immunohistochemical expression of OCT-4
and SOX-2 and to determine their use in differentiating giant cell tumor (GCT) from
central giant cell granuloma (CGCG) and peripheral giant cell granuloma (PGCG).
Study Design
Formalin-fixed, paraffin-embedded tissue blocks of 10 histopathologically diagnosed
cases of GCT, CGCG, or PGCG were examined for anti–OCT-4 and anti–SOX-2 antibodies.
Nuclear staining of stromal mononuclear cells and multinucleated giant cells was considered
positive for OCT-4 and SOX-2 expression.
Results
Nuclear immunoexpression of OCT-4 in stromal mononuclear cells was observed in 80%
(8 of 10) of GCT cases, whereas none of the CGCG and PGCG cases showed OCT-4 immunoreactivity.
SOX-2 immunoreactivity was negative in GCT, CGCG, and PGCG.
Conclusions
OCT-4 immunopositivity in GCT can be used as a cancer stem cell marker to differentiate
GCT from CGCG and PGCG. The presence of OCT-4 in GCT versus its complete absence in
CGCG and PGCG suggests that these three conditions are separate entities. The absence
of stem cell marker OCT-4 and SOX-2 raises questions regarding their role in the pathogenesis
of CGCG and PGCG.
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Article info
Publication history
Published online: May 31, 2020
Accepted:
March 31,
2020
Received in revised form:
February 25,
2020
Received:
November 14,
2019
Identification
Copyright
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