Cargando…
A spontaneous bilateral fallopian tube pregnancy with didelphic uterus: A case report
RATIONALE: In this article, we report interesting clinical manifestation of spontaneous bilateral fallopian tube pregnancies in a patient with a didelphic uterus. PATIENT CONCERNS: A 26-year-old female patient, gravida 2, para 0 + 1, suffered from progressive abdominal pain and vaginal bleeding. A l...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7808534/ https://www.ncbi.nlm.nih.gov/pubmed/33466216 http://dx.doi.org/10.1097/MD.0000000000024291 |
_version_ | 1783636919830183936 |
---|---|
author | Zeng, Xi Luo, Li Ou-Yang, Yun-Wei |
author_facet | Zeng, Xi Luo, Li Ou-Yang, Yun-Wei |
author_sort | Zeng, Xi |
collection | PubMed |
description | RATIONALE: In this article, we report interesting clinical manifestation of spontaneous bilateral fallopian tube pregnancies in a patient with a didelphic uterus. PATIENT CONCERNS: A 26-year-old female patient, gravida 2, para 0 + 1, suffered from progressive abdominal pain and vaginal bleeding. A laboratory exam revealed a human chorionic gonadotropin level of 1091 IU/L. Transvaginal ultrasound detected no embryo sacs in the uterus but revealed a didelphic uterus, and a mass measuring 39 mm x 32 mm in the left adnexa region with another mass measuring 42 x 28 mm in the right adnexa region. DIAGNOSES: An ectopic pregnancy in the left adnexa region and a corpus hemorrhagicum in the right adnexa region were suspected. INTERVENTIONS: Laparoscopic exploration operation confirmed a didelphic uterus, and pathological biopsy revealed bilateral fallopian tube pregnancies. OUTCOMES: The patient made a good recovery and the human chorionic gonadotropin became normal within the following 2 months. LESSONS: To the best of our knowledge, clinical manifestation of spontaneous bilateral fallopian tube pregnancies in a patient with a didelphic uterus has never been reported before. Based on the experience with this case, we suggest that if a gestational sac is found in 1 fallopian tube, the contralateral fallopian tube needs to be examined for an ectopic pregnancy during surgery. |
format | Online Article Text |
id | pubmed-7808534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-78085342021-01-21 A spontaneous bilateral fallopian tube pregnancy with didelphic uterus: A case report Zeng, Xi Luo, Li Ou-Yang, Yun-Wei Medicine (Baltimore) 5600 RATIONALE: In this article, we report interesting clinical manifestation of spontaneous bilateral fallopian tube pregnancies in a patient with a didelphic uterus. PATIENT CONCERNS: A 26-year-old female patient, gravida 2, para 0 + 1, suffered from progressive abdominal pain and vaginal bleeding. A laboratory exam revealed a human chorionic gonadotropin level of 1091 IU/L. Transvaginal ultrasound detected no embryo sacs in the uterus but revealed a didelphic uterus, and a mass measuring 39 mm x 32 mm in the left adnexa region with another mass measuring 42 x 28 mm in the right adnexa region. DIAGNOSES: An ectopic pregnancy in the left adnexa region and a corpus hemorrhagicum in the right adnexa region were suspected. INTERVENTIONS: Laparoscopic exploration operation confirmed a didelphic uterus, and pathological biopsy revealed bilateral fallopian tube pregnancies. OUTCOMES: The patient made a good recovery and the human chorionic gonadotropin became normal within the following 2 months. LESSONS: To the best of our knowledge, clinical manifestation of spontaneous bilateral fallopian tube pregnancies in a patient with a didelphic uterus has never been reported before. Based on the experience with this case, we suggest that if a gestational sac is found in 1 fallopian tube, the contralateral fallopian tube needs to be examined for an ectopic pregnancy during surgery. Lippincott Williams & Wilkins 2021-01-15 /pmc/articles/PMC7808534/ /pubmed/33466216 http://dx.doi.org/10.1097/MD.0000000000024291 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | 5600 Zeng, Xi Luo, Li Ou-Yang, Yun-Wei A spontaneous bilateral fallopian tube pregnancy with didelphic uterus: A case report |
title | A spontaneous bilateral fallopian tube pregnancy with didelphic uterus: A case report |
title_full | A spontaneous bilateral fallopian tube pregnancy with didelphic uterus: A case report |
title_fullStr | A spontaneous bilateral fallopian tube pregnancy with didelphic uterus: A case report |
title_full_unstemmed | A spontaneous bilateral fallopian tube pregnancy with didelphic uterus: A case report |
title_short | A spontaneous bilateral fallopian tube pregnancy with didelphic uterus: A case report |
title_sort | spontaneous bilateral fallopian tube pregnancy with didelphic uterus: a case report |
topic | 5600 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7808534/ https://www.ncbi.nlm.nih.gov/pubmed/33466216 http://dx.doi.org/10.1097/MD.0000000000024291 |
work_keys_str_mv | AT zengxi aspontaneousbilateralfallopiantubepregnancywithdidelphicuterusacasereport AT luoli aspontaneousbilateralfallopiantubepregnancywithdidelphicuterusacasereport AT ouyangyunwei aspontaneousbilateralfallopiantubepregnancywithdidelphicuterusacasereport AT zengxi spontaneousbilateralfallopiantubepregnancywithdidelphicuterusacasereport AT luoli spontaneousbilateralfallopiantubepregnancywithdidelphicuterusacasereport AT ouyangyunwei spontaneousbilateralfallopiantubepregnancywithdidelphicuterusacasereport |