Giant plancental chorioangioma, case report

Authors

  • Marta Rondón Tapia Médica cirujana, Residente del Post-grado de Ginecología y Obstetricia, Servicio de Obstetricia y Ginecología - Maternidad "Dr. Nerio Belloso", Hospital Central "Dr. Urquinaona", Maracaibo, Estado Zulia, Venezuela
  • Eduardo Reyna Villasmil Doctor en Ciencias Médicas, Especialista en Ginecología y Obstetricia, Servicio de Obstetricia y Ginecología - Maternidad "Dr. Nerio Belloso", Hospital Central "Dr. Urquinaona", Maracaibo, Estado Zulia, Venezuela
  • Duly Torres Cepeda Doctor en Ciencias Médicas, Especialista en Ginecología y Obstetricia, Servicio de Obstetricia y Ginecología - Maternidad "Dr. Nerio Belloso", Hospital Central "Dr. Urquinaona", Maracaibo, Estado Zulia, Venezuela

DOI:

https://doi.org/10.31403/rpgo.v62i1950

Abstract

Placental chorioangiomas are benign vascular tumors and are the most common placental tumors, with a prevalence of 1%. It rarely surpasses 4 - 5 centimeters in length and, when it happens, is referred to as giant chorioangioma. Pregnancies with giant chorioangiomas are associated with maternal and fetal complications, such as severe microangiopathic haemolytic anemia, preterm labor, polyhidramnios, intrauterine growth restriction, thrombocytopenia and hydrops. A case of giant chorioangioma diagnosed at 22 weeks is presented. Despite close follow-up, delivery occurred at 30 weeks of pregnancy due to polyhidramnios and premature rupture of membranes. Both mother and newborn recovered without complications.

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Published

2017-01-09

How to Cite

Rondón Tapia, M., Reyna Villasmil, E., & Torres Cepeda, D. (2017). Giant plancental chorioangioma, case report. The Peruvian Journal of Gynecology and Obstetrics, 62(4), 455–458. https://doi.org/10.31403/rpgo.v62i1950

Issue

Section

Casos Clínicos

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