Mixed ovarian epithelial carcinomas with clear cell and serous components are variants of high-grade serous carcinoma: An interobserver correlative and immunohistochemical study of 32 cases Journal Article


Authors: Han, G.; Gilks, C. B.; Leung, S.; Ewanowich, C. A.; Irving, J. A.; Longacre, T. A.; Soslow, R. A.
Article Title: Mixed ovarian epithelial carcinomas with clear cell and serous components are variants of high-grade serous carcinoma: An interobserver correlative and immunohistochemical study of 32 cases
Abstract: There are conflicting data about chemoresistance and prognosis in ovarian clear cell carcinoma (CCC). This could be due to significant interobserver variation in the diagnosis of CCC and other ovarian surface epithelial tumors containing clear cells. Thirty-two cases previously diagnosed as CCC, high-grade ovarian serous carcinoma (SC), and mixed surface epithelial carcinoma (SEC) with clear cell and serous components were reviewed by 4 gynecologic pathologists blinded to the original diagnoses. Interobserver reproducibility was evaluated. Each case was also assessed using immunohistochemical markers Wilm tumor 1, estrogen receptor, and p53. The interobserver reproducibility was greatest for pure CCC (κ of 0.82), and lowest for the mixed SEC (κ of 0.32). Moderate agreement was seen in the pure SC category (κ of 0.59). All pure SC and most mixed SEC presented as stage III or IV diseases. Most pure CCC presented as stage I or II diseases. Immunoreactivities of the mixed SECs were similar to those of pure SC, but significantly different from those of pure CCC for Wilm tumor 1 (P=0.0011 for both components), estrogen receptor (P=0.0003 for clear cell component, P=0.0001 for serous component), and p53 (P=0.0062 for both components). The serous and clear cell components of mixed SEC showed higher mitotic rates than pure CCC (P=0.004 and P=0.023, respectively), but the mitotic rate of pure SC was similar to the mixed SEC. We conclude that (1) pure CCC is reproducibly diagnosed. (2) The diagnosis of mixed ovarian SEC with clear cell component is not reproducible. (3) Mixed SEC with clear cell and serous components show similar stage, mitotic activities, and immunoreactivities to those of pure SC, and likely represent SC with clear cell changes. © 2008 by Lippincott Williams & Wilkins.
Keywords: immunohistochemistry; clinical article; controlled study; human tissue; middle aged; unclassified drug; cancer staging; neoplasm staging; cancer grading; adenocarcinoma; mitosis; ovarian neoplasms; reproducibility; biological marker; reproducibility of results; apoptosis; observer variation; tumor markers, biological; pathology; immunoreactivity; protein p53; tumor marker; chemistry; ovary tumor; carcinoma; ovary carcinoma; clear cell carcinoma; ovarian carcinoma; adenocarcinoma, clear cell; cystadenocarcinoma, serous; estrogen receptor; multiple cancer; neoplasms, multiple primary; serous carcinoma; cystadenocarcinoma; mixed epithelial carcinoma; clear cell; serous; diagnostic reproducibility; protein wilm tumo 1
Journal Title: American Journal of Surgical Pathology
Volume: 32
Issue: 7
ISSN: 0147-5185
Publisher: Lippincott Williams & Wilkins  
Date Published: 2008-07-01
Start Page: 955
End Page: 964
Language: English
DOI: 10.1097/PAS.0b013e318164edf7
PUBMED: 18460981
PROVIDER: scopus
DOI/URL:
Notes: --- - "Cited By (since 1996): 13" - "Export Date: 17 November 2011" - "CODEN: AJSPD" - "Source: Scopus"
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
  1. Robert Soslow
    793 Soslow