No. 32 (2025): Jul - Sep
Case Report

Bilateral Axillary Polymastia - Clinical Case

Joana Duarte Teixeira
USF do Villa, São Braz de Alportel
Marta Mendonça
USF do Villa, São Braz de Alportel

Published 04/09/2026

Keywords

  • pregnancy,
  • subclinical hyperthyroidism,
  • iron deficiency anemia,
  • accessory breast tissue,
  • umbilical cord prolapse,
  • emergent cesarean section
  • ...More
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How to Cite

1.
Duarte Teixeira J, Mendonça M. Bilateral Axillary Polymastia - Clinical Case. Alg Med [Internet]. 2026 Apr. 9 [cited 2026 Apr. 18];(32):30-3. Available from: https://algarvemedico.org/index.php/am/article/view/21

Abstract

We report the case of a 25-year-old woman with a history of subclinical hyperthyroidism, chronic iron deficiency anemia, and anxiety, followed throughout her first pregnancy. During gestation, bilateral axillary accessory breast tissue was detected and confirmed by breast ultrasound (BI-RADS 1). Pregnancy was globally uneventful, with occasional discomfort, fatigue, and Braxton Hicks contractions in the third trimester. At 37+3 weeks, premature rupture of membranes complicated by umbilical cord prolapse led to an emergent cesarean section for fetal distress. The male newborn weighed 2770 g with an Apgar score of 10/10. In the early postpartum period, the mother opted for lactation inhibition with cabergoline due to symptomatic enlargement of accessory breast tissue. This case highlights the importance of integrated monitoring of pre-existing conditions, proper investigation of uncommon clinical findings, and prompt obstetric intervention in emergencies.

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