Uterine hemangioma in pregnancy: A case report and review of the literature.
Case report
Hemangioma
Pregnancy
Review
Uterine
Journal
Journal of gynecology obstetrics and human reproduction
ISSN: 2468-7847
Titre abrégé: J Gynecol Obstet Hum Reprod
Pays: France
ID NLM: 101701588
Informations de publication
Date de publication:
Jun 2022
Jun 2022
Historique:
received:
01
03
2022
revised:
24
04
2022
accepted:
26
04
2022
pubmed:
2
5
2022
medline:
25
5
2022
entrez:
1
5
2022
Statut:
ppublish
Résumé
Uterine hemangioma is a rare benign vascular tumor which can cause bleeding problems in various age groups. Current knowledge on this rare condition in pregnancy is limited. We report on a recent case of uterine hemangioma in a pregnancy that was already diagnosed during her first trimester. We also provide a literature review to summarize the characteristics and outcomes of uterine hemangioma cases in pregnant women. A systematic search was done of all published literature up to February 2021 using PubMed and Scopus databases. The selection process was registered using the online tool Rayyan QCRI. All data was described in a narrative format. The protocol was prospectively registered on PROSPERO (CRD42021237519). Fifteen case reports were included. In most cases, the diagnosis was established by antenatal ultrasound. More than half of the women developed a postpartum hemorrhage, necessitating a hysterectomy for bleeding control in half of the cases, although the risk for both seemed lower in those women in whom the hemangioma was diagnosed before delivery. One case of maternal mortality and two cases of fetal death were reported. There was one case of neonatal respiratory morbidity, although the neonatal data were not routinely reported upon. Current knowledge on uterine hemangioma in pregnancy is limited, but it seems to hold substantial risks for both pregnant women and their unborn child. We recommend routine screening for this condition at the standard mid-trimester anomaly scan. Pregnant women with uterine hemangioma should ideally be cared for in centers of expertise. An international registry will help to build a better understanding of this rare pathology.
Identifiants
pubmed: 35490987
pii: S2468-7847(22)00084-8
doi: 10.1016/j.jogoh.2022.102401
pii:
doi:
Types de publication
Case Reports
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
102401Informations de copyright
Copyright © 2022 The Author(s). Published by Elsevier Masson SAS.. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest No potential competing interest was reported by the authors.