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Spontaneous Heterotopic Pregnancy: Diagnosis and Management

BACKGROUND: Heterotopic pregnancies albeit rare are conceivably life-threatening if missed. With the development of assisted reproductive techniques, the incidence has increased. Confirmation of an intrauterine pregnancy (IUP) should not preclude the existence of a heterotopic pregnancy. CASE: A hea...

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Detalles Bibliográficos
Autores principales: Nguyen, Katie P., Hudspeth, Marlekah, Milestone, Honey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9345693/
https://www.ncbi.nlm.nih.gov/pubmed/35928785
http://dx.doi.org/10.1155/2022/2994808
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author Nguyen, Katie P.
Hudspeth, Marlekah
Milestone, Honey
author_facet Nguyen, Katie P.
Hudspeth, Marlekah
Milestone, Honey
author_sort Nguyen, Katie P.
collection PubMed
description BACKGROUND: Heterotopic pregnancies albeit rare are conceivably life-threatening if missed. With the development of assisted reproductive techniques, the incidence has increased. Confirmation of an intrauterine pregnancy (IUP) should not preclude the existence of a heterotopic pregnancy. CASE: A healthy 27-year-old patient (gravida 4, term 1, preterm 0, abortion 2, living 1) at approximately 5 weeks gestation through natural conception presented to the emergency room with acute abdominal pain and vaginal bleeding. Pelvic ultrasound showed evidence of an IUP and a right adnexal mass, raising suspicion for a heterotopic pregnancy. The patient underwent an uncomplicated laparoscopic right salpingectomy. An IUP was confirmed on ultrasound postoperatively. The patient had an early pregnancy loss at 8 weeks of gestation. CONCLUSION: With a high index of suspicion from clinical presentation and pelvic imaging, heterotopic pregnancy, while rare, should not be ruled out.
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spelling pubmed-93456932022-08-03 Spontaneous Heterotopic Pregnancy: Diagnosis and Management Nguyen, Katie P. Hudspeth, Marlekah Milestone, Honey Case Rep Obstet Gynecol Case Report BACKGROUND: Heterotopic pregnancies albeit rare are conceivably life-threatening if missed. With the development of assisted reproductive techniques, the incidence has increased. Confirmation of an intrauterine pregnancy (IUP) should not preclude the existence of a heterotopic pregnancy. CASE: A healthy 27-year-old patient (gravida 4, term 1, preterm 0, abortion 2, living 1) at approximately 5 weeks gestation through natural conception presented to the emergency room with acute abdominal pain and vaginal bleeding. Pelvic ultrasound showed evidence of an IUP and a right adnexal mass, raising suspicion for a heterotopic pregnancy. The patient underwent an uncomplicated laparoscopic right salpingectomy. An IUP was confirmed on ultrasound postoperatively. The patient had an early pregnancy loss at 8 weeks of gestation. CONCLUSION: With a high index of suspicion from clinical presentation and pelvic imaging, heterotopic pregnancy, while rare, should not be ruled out. Hindawi 2022-07-26 /pmc/articles/PMC9345693/ /pubmed/35928785 http://dx.doi.org/10.1155/2022/2994808 Text en Copyright © 2022 Katie P. Nguyen et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Nguyen, Katie P.
Hudspeth, Marlekah
Milestone, Honey
Spontaneous Heterotopic Pregnancy: Diagnosis and Management
title Spontaneous Heterotopic Pregnancy: Diagnosis and Management
title_full Spontaneous Heterotopic Pregnancy: Diagnosis and Management
title_fullStr Spontaneous Heterotopic Pregnancy: Diagnosis and Management
title_full_unstemmed Spontaneous Heterotopic Pregnancy: Diagnosis and Management
title_short Spontaneous Heterotopic Pregnancy: Diagnosis and Management
title_sort spontaneous heterotopic pregnancy: diagnosis and management
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9345693/
https://www.ncbi.nlm.nih.gov/pubmed/35928785
http://dx.doi.org/10.1155/2022/2994808
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