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Recurrent, Idiopathic Spontaneous Hemoperitoneum Requiring Multiple Laparoscopic Evacuations: A Rare Case of Bleeding Adnexal Arteriovenous Malformation
Arteriovenous malformations (AVMs) are abnormal vascular connections that can form in many anatomic locations. The adnexa are particularly rare sites of AVM formation and the symptomatology is heterogeneous. Herein we present a case of life-threatening adnexal AVM. A 21-year-old female presented wit...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812936/ https://www.ncbi.nlm.nih.gov/pubmed/31656716 http://dx.doi.org/10.7759/cureus.5490 |
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author | Assimacopoulos, Aikaterina Mehta, Tej I Brockmeier, Catherine Yim, Douglas |
author_facet | Assimacopoulos, Aikaterina Mehta, Tej I Brockmeier, Catherine Yim, Douglas |
author_sort | Assimacopoulos, Aikaterina |
collection | PubMed |
description | Arteriovenous malformations (AVMs) are abnormal vascular connections that can form in many anatomic locations. The adnexa are particularly rare sites of AVM formation and the symptomatology is heterogeneous. Herein we present a case of life-threatening adnexal AVM. A 21-year-old female presented with abdominal pain and syncope, her third such presentation within 10 days. Her history was significant for ectopic pregnancy six months prior. Diagnostic laparoscopy revealed intraperitoneal blood without active bleeding. Transabdominal pelvic ultrasound revealed a large amount of complicated pelvic fluid and increased right-adnexal vascularity. Interventional radiology performed an urgent uterine arteriogram revealing a right-adnexal AVM with supply from both the right uterine and right ovarian arteries. The AVM was subsequently embolized, resolving her symptoms. AVMs are exceedingly rare, often unconsidered causes of occult pelvic bleeding. Pelvic, and in particular, adnexal AVMs should be considered in females with idiopathic spontaneous hemoperitoneum. |
format | Online Article Text |
id | pubmed-6812936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-68129362019-10-25 Recurrent, Idiopathic Spontaneous Hemoperitoneum Requiring Multiple Laparoscopic Evacuations: A Rare Case of Bleeding Adnexal Arteriovenous Malformation Assimacopoulos, Aikaterina Mehta, Tej I Brockmeier, Catherine Yim, Douglas Cureus Radiology Arteriovenous malformations (AVMs) are abnormal vascular connections that can form in many anatomic locations. The adnexa are particularly rare sites of AVM formation and the symptomatology is heterogeneous. Herein we present a case of life-threatening adnexal AVM. A 21-year-old female presented with abdominal pain and syncope, her third such presentation within 10 days. Her history was significant for ectopic pregnancy six months prior. Diagnostic laparoscopy revealed intraperitoneal blood without active bleeding. Transabdominal pelvic ultrasound revealed a large amount of complicated pelvic fluid and increased right-adnexal vascularity. Interventional radiology performed an urgent uterine arteriogram revealing a right-adnexal AVM with supply from both the right uterine and right ovarian arteries. The AVM was subsequently embolized, resolving her symptoms. AVMs are exceedingly rare, often unconsidered causes of occult pelvic bleeding. Pelvic, and in particular, adnexal AVMs should be considered in females with idiopathic spontaneous hemoperitoneum. Cureus 2019-08-26 /pmc/articles/PMC6812936/ /pubmed/31656716 http://dx.doi.org/10.7759/cureus.5490 Text en Copyright © 2019, Assimacopoulos et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Radiology Assimacopoulos, Aikaterina Mehta, Tej I Brockmeier, Catherine Yim, Douglas Recurrent, Idiopathic Spontaneous Hemoperitoneum Requiring Multiple Laparoscopic Evacuations: A Rare Case of Bleeding Adnexal Arteriovenous Malformation |
title | Recurrent, Idiopathic Spontaneous Hemoperitoneum Requiring Multiple Laparoscopic Evacuations: A Rare Case of Bleeding Adnexal Arteriovenous Malformation |
title_full | Recurrent, Idiopathic Spontaneous Hemoperitoneum Requiring Multiple Laparoscopic Evacuations: A Rare Case of Bleeding Adnexal Arteriovenous Malformation |
title_fullStr | Recurrent, Idiopathic Spontaneous Hemoperitoneum Requiring Multiple Laparoscopic Evacuations: A Rare Case of Bleeding Adnexal Arteriovenous Malformation |
title_full_unstemmed | Recurrent, Idiopathic Spontaneous Hemoperitoneum Requiring Multiple Laparoscopic Evacuations: A Rare Case of Bleeding Adnexal Arteriovenous Malformation |
title_short | Recurrent, Idiopathic Spontaneous Hemoperitoneum Requiring Multiple Laparoscopic Evacuations: A Rare Case of Bleeding Adnexal Arteriovenous Malformation |
title_sort | recurrent, idiopathic spontaneous hemoperitoneum requiring multiple laparoscopic evacuations: a rare case of bleeding adnexal arteriovenous malformation |
topic | Radiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812936/ https://www.ncbi.nlm.nih.gov/pubmed/31656716 http://dx.doi.org/10.7759/cureus.5490 |
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