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A unique case of diagnosis of a heterotopic pregnancy at 26 weeks – case report and literature review
BACKGROUND: Heterotopic pregnancy (HP) is a rare condition when at least two pregnancies are present simultaneously at different implantation sites and only one located in the uterine cavity. The majority of cases are diagnosed in the first trimester. CASE PRESENTATION: We present a unique case of H...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814709/ https://www.ncbi.nlm.nih.gov/pubmed/33461507 http://dx.doi.org/10.1186/s12884-020-03465-y |
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author | Kajdy, Anna Muzyka-Placzyńska, Katarzyna Filipecka-Tyczka, Dagmara Modzelewski, Jan Stańczyk, Marek Rabijewski, Michał |
author_facet | Kajdy, Anna Muzyka-Placzyńska, Katarzyna Filipecka-Tyczka, Dagmara Modzelewski, Jan Stańczyk, Marek Rabijewski, Michał |
author_sort | Kajdy, Anna |
collection | PubMed |
description | BACKGROUND: Heterotopic pregnancy (HP) is a rare condition when at least two pregnancies are present simultaneously at different implantation sites and only one located in the uterine cavity. The majority of cases are diagnosed in the first trimester. CASE PRESENTATION: We present a unique case of HP diagnosed at 26 weeks of spontaneous pregnancy in a patient without any relevant risk factors. We performed an extensive review of HP cases from MEDLINE (PUBMED) published in English between 2005-2019 to prove this case's uniqueness. A 24-year-old woman presented because of threatened preterm birth. Despite treatment, pain aggravated, without progression of labor. An emergency ultrasound exam revealed free fluid in the abdominal cavity. Suspicion of active bleeding prompted the medical team to perform an exploratory laparotomy. The surgery team found a ruptured heterotopic pregnancy. This was an unexpected cause of nontraumatic hemoperitoneum at such advanced gestational age. The postoperative period was uneventful, and the intrauterine pregnancy continued to term. The final review included 86 out of 124 records. A total number of 509 cases were identified, but not all of them had complete data. The maximum reported gestational age at the time of diagnosis was 16 weeks of pregnancy, while our case became symptomatic and was diagnosed at 26 weeks of pregnancy. CONCLUSIONS: Regardless of pregnancy age, HP can be a cause of hemoperitoneum, and it should be included in the differential diagnosis of acute abdomen in the second trimester. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12884-020-03465-y. |
format | Online Article Text |
id | pubmed-7814709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78147092021-01-21 A unique case of diagnosis of a heterotopic pregnancy at 26 weeks – case report and literature review Kajdy, Anna Muzyka-Placzyńska, Katarzyna Filipecka-Tyczka, Dagmara Modzelewski, Jan Stańczyk, Marek Rabijewski, Michał BMC Pregnancy Childbirth Case Report BACKGROUND: Heterotopic pregnancy (HP) is a rare condition when at least two pregnancies are present simultaneously at different implantation sites and only one located in the uterine cavity. The majority of cases are diagnosed in the first trimester. CASE PRESENTATION: We present a unique case of HP diagnosed at 26 weeks of spontaneous pregnancy in a patient without any relevant risk factors. We performed an extensive review of HP cases from MEDLINE (PUBMED) published in English between 2005-2019 to prove this case's uniqueness. A 24-year-old woman presented because of threatened preterm birth. Despite treatment, pain aggravated, without progression of labor. An emergency ultrasound exam revealed free fluid in the abdominal cavity. Suspicion of active bleeding prompted the medical team to perform an exploratory laparotomy. The surgery team found a ruptured heterotopic pregnancy. This was an unexpected cause of nontraumatic hemoperitoneum at such advanced gestational age. The postoperative period was uneventful, and the intrauterine pregnancy continued to term. The final review included 86 out of 124 records. A total number of 509 cases were identified, but not all of them had complete data. The maximum reported gestational age at the time of diagnosis was 16 weeks of pregnancy, while our case became symptomatic and was diagnosed at 26 weeks of pregnancy. CONCLUSIONS: Regardless of pregnancy age, HP can be a cause of hemoperitoneum, and it should be included in the differential diagnosis of acute abdomen in the second trimester. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12884-020-03465-y. BioMed Central 2021-01-18 /pmc/articles/PMC7814709/ /pubmed/33461507 http://dx.doi.org/10.1186/s12884-020-03465-y Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Kajdy, Anna Muzyka-Placzyńska, Katarzyna Filipecka-Tyczka, Dagmara Modzelewski, Jan Stańczyk, Marek Rabijewski, Michał A unique case of diagnosis of a heterotopic pregnancy at 26 weeks – case report and literature review |
title | A unique case of diagnosis of a heterotopic pregnancy at 26 weeks – case report and literature review |
title_full | A unique case of diagnosis of a heterotopic pregnancy at 26 weeks – case report and literature review |
title_fullStr | A unique case of diagnosis of a heterotopic pregnancy at 26 weeks – case report and literature review |
title_full_unstemmed | A unique case of diagnosis of a heterotopic pregnancy at 26 weeks – case report and literature review |
title_short | A unique case of diagnosis of a heterotopic pregnancy at 26 weeks – case report and literature review |
title_sort | unique case of diagnosis of a heterotopic pregnancy at 26 weeks – case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814709/ https://www.ncbi.nlm.nih.gov/pubmed/33461507 http://dx.doi.org/10.1186/s12884-020-03465-y |
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