کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
105231 161506 2012 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Immunohistochemical expression and prognostic significance of oestrogen receptor-alpha, oestrogen receptor-beta, and progesterone receptor in stage 1 adult-type granulosa cell tumour of the ovary
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی پزشکی قانونی
پیش نمایش صفحه اول مقاله
Immunohistochemical expression and prognostic significance of oestrogen receptor-alpha, oestrogen receptor-beta, and progesterone receptor in stage 1 adult-type granulosa cell tumour of the ovary
چکیده انگلیسی

SummaryAimsTo assess oestrogen receptor (ER)α, ERβ, and progesterone receptor (PR) expression in stage I ovarian adult-type granulosa cell tumours (AGCTs) and correlate the findings with clinical outcome.MethodsERα, ERβ and PR immunohistochemistry was performed on 56 primary, stage I AGCTs. Twelve cases (21%) recurred and hormone receptor staining was compared in the corresponding primary and metastatic tumours.ResultsAll primary AGCTs expressed ERβ and PR, usually with strong and diffuse staining, whereas only 20% of tumours were focally ERα positive. There was no correlation between ERα or PR expression and outcome. However, primary AGCTs with low ERβ expression had a significantly higher risk of recurrence. In contrast, all metastatic tumours exhibited strong ERβ staining. No relationship between ER staining and tumour morphology was identified but there was more consistent PR expression in cells at the tumour-stromal interface.ConclusionsPrimary AGCTs typically show an ERα negative and ERβ/PR positive immunophenotype. Low ERβ expression is an adverse prognostic factor in primary AGCT but metastatic tumours often show up-regulation of ERβ. Local microenvironmental factors may influence PR expression. Hormone receptor expression in AGCT may become increasingly relevant due to developments in selective therapy.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Pathology - Volume 44, Issue 7, December 2012, Pages 611-616