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Ginecología y obstetricia de México

versión impresa ISSN 0300-9041

Resumen

CASTILLO-ROSALES, Silda; GONZALEZ-PADRON, Elena; VELASQUEZ-CASTELLANOS, Patricia Inés  y  MACIAS-VERA, Norah Nalleli. Buschke-Löwenstein tumor resection in a pregnant women: A case report and literature review. Ginecol. obstet. Méx. [online]. 2022, vol.90, n.12, pp.1010-1016.  Epub 14-Abr-2023. ISSN 0300-9041.  https://doi.org/10.24245/gom.v90i12.5247.

BACKGROUND:

Buschke-Löwenstein tumor is associatted with the human papillomavirus (HPV), which is considered a sexually transmitted infection, characterized by the presence of a giant wart, exophytic condyloma with the shape of a cauliflower, slow growth, but during pregnancy it can grow fast as a solitary condyloma, affecting other structures. This case provides a better understanding of an unusual pathology, which with surgical treatment was obtained aesthetic results and with adequate functionality of external genitalia.

CLINICAL CASE

18-year-old female, primiparous with 35 weeks pregnant, with no significant history, 4 previous months begins with the presence of warts in the perineal region with accelerated increase in size in the last 30 days, associated with intense pain on mobilization, fetid discharge, and area oferythema and intergluteal irritation, friable tumor with a tendency to bleed with areas of necrosis.

CONCLUSIONS:

The Buschke-Löwenstein tumor is a rare pathology caused by HPV, which can present accelerated growth due to the hormonal stimulus of the gestational state, this tumor does not resolve spontaneously, so the surgical approach is considered top of the line. The follow-up of these patients must be close due to the high rate of recurrence.

Palabras llave : Buschke-Löwenstein tumor; giant condyloma; Human Papillomavirus; wart.

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