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Combination of cervical cancer and unilateral complete aplasia of the adnexa: a case report

https://doi.org/10.20538/1682-0363-2019-2-299-303

Abstract

We  present  a  rare  case  of  the  combination   of  cervical  cancer  and  unilateral complete   aplasia  of  the uterine  adnexa.    Female  genital  tract anomalies  account  for  about  4% of all congenital  malformations.

Congenital  malformations  of the  adnexa  are  very  rare,  accounting  for  less than  0.5%. In  the  presented case, this abnormality was found incidentally during surgery for cervical cancer. Medical genetic counseling confirmed  the presence  of the isolated congenital  pathology.

About the Authors

A. L. Chernyshova
Cancer Research Institute, Tomsk National Research Medical Center (TNRMC) SO RAS
Russian Federation

Chernyshova Alyona L. - DM, Senior  Research  Scientist, Gynecology Department, Cancer Research Institute, TNRMC.

5 Kooperativny lane, 634050, Tomsk.



L. A. Kolomiets
Cancer Research Institute, Tomsk National Research Medical Center (TNRMC) SO RAS
Russian Federation

Kolomiets  Larisa  A. - DM,  Professor,   Head  of Gynecology Department, Cancer Research Institute, TNRMC.

5 Kooperativny lane, 634050, Tomsk.



A. Yu. Kishkina
Cancer Research Institute, Tomsk National Research Medical Center (TNRMC) SO RAS
Russian Federation

Kishkina  Anastasia  Yu. - Postgraduate  Student, Gynecology Department, Cancer Research Institute.

5 Kooperativny lane, 634050, Tomsk.



М. O. Ochirov
Cancer Research Institute, Tomsk National Research Medical Center (TNRMC) SO RAS
Russian Federation

Ochirov  Maxim O. - Postgraduate Student,  Gynecology Department, Cancer Research Institute, TNRMC.

5 Kooperativny lane, 634050, Tomsk.



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Review

For citations:


Chernyshova A.L., Kolomiets L.A., Kishkina A.Yu., Ochirov М.O. Combination of cervical cancer and unilateral complete aplasia of the adnexa: a case report. Bulletin of Siberian Medicine. 2019;18(2):299-303. https://doi.org/10.20538/1682-0363-2019-2-299-303

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ISSN 1682-0363 (Print)
ISSN 1819-3684 (Online)