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Original Research

Chlamydia trachomatis infection in primary fallopian tube and high-grade serous ovarian cancers: a pilot study

, , , , , , , , & show all
Pages 199-205 | Published online: 22 Mar 2019
 

Abstract

Background

The aim of this study was to evaluate the association of Chlamydia trachomatis (CT) infection with primary tubal and high-grade serous ovarian cancers.

Methods

This is a cross-sectional, retrospective study conducted at Ain Shams University Maternity Hospital, Egypt, from February 2008 to October 2017. Sixty-seven paraffin archival blocks specimens were retrieved from cases who underwent staging laparotomy due to high-grade serous ovarian cancer (30 cases), primary tubal serous cancer (25 cases), and control specimens of (12) tubal specimens from cases of benign gynecological conditions. All samples were examined for CT DNA using semiquantitative qRT-PCR.

Results

CT DNA was detected in 84% of high-grade tubal serous cancer, 16.7% of high-grade serous ovarian cancer, and 13.3% in controls (P<0.0005). Mean CT DNA relative quantity was significantly high (256) in tubal carcinoma, in comparison to that in high-grade serous ovarian cancer and controls (13.5 and 0.28, respectively; P<0.0005).

Conclusion

To the best of our knowledge, this is the first report on relation of CT to the tubal serous cancer, so the responsibility of CT tubal infection in the pathogenesis of primary tubal cancer needs to be considered.

Supplementary materials

Figure S1 High-grade serous tubal carcinoma is seen distending the tubal lumen (H&E ×10).

Figure S1 High-grade serous tubal carcinoma is seen distending the tubal lumen (H&E ×10).

Figure S2 High-grade serous tubal carcinoma arises from tubal mucosa and infiltrates the submucosa (H&E ×10).

Figure S2 High-grade serous tubal carcinoma arises from tubal mucosa and infiltrates the submucosa (H&E ×10).

Disclosure

The authors report no conflicts of interest in this work.