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Brenner Tumors, Pathology of the Ovary

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Encyclopedia of Pathology

Part of the book series: Encyclopedia of Pathology ((EP))

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Benign Brenner Tumor

Definition

Benign Brenner tumor is a rare neoplasm with unknown etiology, deriving through metaplasia of the ovarian surface epithelium, from metaplastic transitional epithelium (Walthard nests) located in the hilar region of the ovary or beneath the serosa of the fallopian tube or from a teratoma. Benign Brenner tumor is composed of bland transitional-type epithelium, proliferating in a dense fibromatous stroma.

Clinical Features

  • Incidence

    Benign Brenner tumor is a rare condition in the ovary representing approximately 5% of all benign epithelial tumors (Herrington et al. 2020).

  • Age

    The tumor usually occurs in adult patients (fifth–seventh decade of life) but can develop at any age (Herrington et al. 2020).

  • Sex

    Female.

  • Site

    Ovary.

  • Treatment

    Surgical excision is indicated and is curative.

  • Outcome

    The tumor has no risk of recurrence or progression.

Macroscopy

Benign Brenner tumor is usually unilateral (with less than 10% being bilateral) and small (<2 cm), being...

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References and Further Reading

  • Esheba, G. E., Longacre, T. A., Atkins, K. A., et al. (2009). Expression of the urothelial differentiation markers GATA3 and placental S100 (S100P) in female genital tract transitional cell proloferation. The American Journal of Surgical Pathology, 33(3), 347–353.

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  • Herrington, C. S., Kim, K. R., Kong, C., et al. (2020). Tumours of the uterine cervix. W. C. o. T. E. B. F. g. tumours (pp. 336–389). Lyon: International Agency for Research on Cancer.

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  • Nasioudis, D., Sisti, G., Holcomb, K., et al. (2016). Malignant Brenner tumors of the ovary; A population-based analysis. Gynecologic Oncology, 142(1), 44–49.

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Stolnicu, S. (2022). Brenner Tumors, Pathology of the Ovary. In: van Krieken, J. (eds) Encyclopedia of Pathology. Encyclopedia of Pathology. Springer, Cham. https://doi.org/10.1007/978-3-319-28845-1_5657-1

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  • DOI: https://doi.org/10.1007/978-3-319-28845-1_5657-1

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  • Print ISBN: 978-3-319-28845-1

  • Online ISBN: 978-3-319-28845-1

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