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DOI 10.1111/cyt.12844

Медицинская библиотека · Cytopathology : official journal of the British Society for Clinical Cytology · 2020

Assessment of micronuclei counts as tumour marker in cervical carcinogenesis: A follow-up study.

Srivastava Anand Narain, Misra Jata Shanker, Ahmad Rumana

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Аннотация

OBJECTIVE

Micronuclei counts were performed in cervical smears with low-grade squamous intraepithelial lesions of the cervix (LSIL) to assess its potentiality as tumour marker in cervical carcinogenesis.

METHODS

The cases studied were from the ongoing rural cervical cancer screening in west Lucknow, India. Micronuclei counts were performed in the cervical smears of 100 LSIL cases, and the number of cells with micronuclei was defined as micronucleated cells (MNC) and the number of micronuclei per 1000 cells as MNC score. Human papillomavirus (HPV) DNA testing was also done in 100 LSIL cases by GeneNav qPCR test.

RESULTS

A high MNC score was found in 20 of the 100 LSIL cases while the counts were low in the remaining 80. Persistence of LSIL was seen in 19 of the 20 LSIL cases with high MNC score while only six cases of the 80 cases with low MNC score showed persistence. The persistence of LSIL was very high in cases with high MNC score. The multiple high-risk HPV types such as 18, 31, 33 and 35 were seen in 12 of the 100 LSIL cases and a high positivity rate was seen in women with high MNC score. The persistence of LSIL was also higher with HPV positivity.

CONCLUSION

The study revealed correlation between high MNC score, persistence of LSIL and HPV positivity. Hence, MNC score can prove to be very useful in discriminating high-risk LSIL cases that are less likely to regress and possibly may progress to high-grade squamous intraepithelial lesions or carcinoma.

Для цитирования: Srivastava Anand Narain, Misra Jata Shanker, Ahmad Rumana. Assessment of micronuclei counts as tumour marker in cervical carcinogenesis: A follow-up study.. Cytopathology : official journal of the British Society for Clinical Cytology. 2020. DOI: 10.1111/cyt.12844.

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