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April 1, 2026Case Reports in Obstetrics and Gynecology0 citationsOpen Access

Bartholin’s Gland Hyperplasia and Type III Female Genital Mutilation: A Clinical Case Report and Literature Perspective

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ADAva DubessetDTDiane TurbergDBDiomidis Botsikas

Key Points

  • To explore the relationship between Bartholin’s gland hyperplasia and female genital mutilation type III in a clinical context.
  • Presented a clinical case of a young female with a left vulvar mass due to Bartholin’s gland hyperplasia.
  • Performed excision of the mass followed by pathological examination to confirm the diagnosis.
  • Reviewed literature to assess the association between FGM/C and Bartholin's gland conditions.
  • Bartholin’s gland hyperplasia was confirmed after excision and examination of the mass.
  • The case suggests that FGM/C may contribute to chronic inflammation leading to gland enlargement.
  • This linkage of Bartholin’s gland hyperplasia to FGM/C is previously unreported.

Abstract

An enlargement of the Bartholin’s gland can be caused by several conditions, both benign and malignant. Bartholin’s gland hyperplasia is a rare and relatively unknown diagnosis that can be overlooked or misdiagnosed due to unspecific clinical presentation. The patient presented in this case report is a young female with a bothersome left vulvar firm mass and a female genital mutilation/cutting (FGM/C) type IIIa. The mass was excised, and a Bartholin’s gland hyperplasia was confirmed by pathological examination. We hypothesize that FGM/C may have been an etiological factor for Bartholin’s gland hyperplasia in this patient, possibly associated with chronic inflammation, and thus is important to consider when presented with a Bartholin’s mass. To our knowledge, Bartholin’s gland hyperplasia associated with FGM represents a previously unreported condition, making this case a unique and valuable addition to the existing literature.

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Cite This Study

Dubesset et al. (2026) studied this question.

synapsesocial.com/papers/69cd7b065652765b073a8b13https://doi.org/10.1155/crog/8830282
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