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Krukenberg Tumour in Adolescents: Rare but Possible

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Abstract

Krukenberg tumour is a rare ovarian metastatic carcinoma arising from a primary malignancy elsewhere, classically the gastrointestinal tract and breast. They are bilateral solid ovarian tumour which most commonly occurs between 40–60 years, and its occurrence in the second decade of life is extremely rare. In this short commentary, we present an unusual case of Krukenberg tumour in a 16-year old in which diagnosis was made intraoperatively and managed systematically, thus emphasising the need to suspect Krukenberg in all age groups.

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Correspondence to Anjana Annal.

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Informed consent was obtained from patient’s parents (as patient is not alive) for using patient’s personal health information in this case report.

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Anjana Annal is a M.B.B.S., M.S., D.N.B., Specialist in the Department of Obstetrics and Gynaecology, Aster Medicity, India; Shameema Anvar Sadath is a M.B.B.S, M.D, D.N.B, MRCOG, FICRS, MNAMS, FRCOG, Senior Consultant in the Department of Obstetrics and Gynaecology, Aster Medicity, India.

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Annal, A., Sadath, S.A. Krukenberg Tumour in Adolescents: Rare but Possible. J Obstet Gynecol India 72, 460–462 (2022). https://doi.org/10.1007/s13224-020-01414-5

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  • DOI: https://doi.org/10.1007/s13224-020-01414-5

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