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Abstract
Ovarian transitional cell tumors include Brenner tumors (BTs) and transitional
cell carcinoma (TCC; non-BTs) according to the most recent World Health
Organization classification. However, it remains a matter of debate
whether TCC represents a distinct entity or a morphologic variant of
high-grade serous adenocarcinoma (HG-SC). The purpose of this study was
to resolve the above question by clarifying the morphologic,
immunohistochemical, and molecular features of TCC. We reviewed 488
cases of epithelial ovarian carcinomas and reclassified them on the
basis of the most recent World Health Organization classification with
the modifications proposed by Köbel and colleagues, and 35 cases of TCC
were identified; 25 and 6 TCCs were admixed with HG-SC and endometrioid
adenocarcinoma (EC), respectively, and the remaining 4 cases were pure
TCC. TCC components were not observed in any clear cell carcinomas or
mucinous adenocarcinomas. Only 2 cases of malignant BT were identified.
In addition to TCCs, malignant BTs, and related adenocarcinomas, benign
and borderline BTs were included in the following immunohistochemical
and molecular analyses. Immunohistochemically, pure TCCs, TCCs admixed
with HG-SC, and pure HG-SCs were characterized by frequent aberrant p53
expression (diffuse or null pattern) and WT1/ER/PR/IMP2 immunophenotype,
whereas BTs, including benign, borderline, and malignant BTs, were
characterized by lack of aberrant p53 expression and WT1/ER/PR/IMP2
immunophenotype. In contrast to the BTs, pure ECs and TCCs admixed with
EC showed an ER/PR immunophenotype. Nearly all the tumors with a TP53
gene mutation by molecular analysis showed aberrant p53 staining
patterns. In conclusion, TCC is not a distinct entity but a poorly
differentiated form of serous or EC, as (1) most TCCs coexist with HG-SC
(mostly) or EC (occasionally), and (2) the immunophenotype and
molecular features are similar to those of HG-SC or EC but different
from those of BTs.
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