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Congenital thrombotic thrombocytopenic purpura (TTP) with placental abruption despite maternal improvement: a case report
BACKGROUND: Thrombotic thrombocytopenic purpura (TTP) is a rare but serious complication in pregnancy that places the mother and fetus at high risk for morbidity and mortality. This case illustrates novel pregnancy complications associated with this rare medical condition. CASE PRESENTATION: A 31-ye...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296940/ https://www.ncbi.nlm.nih.gov/pubmed/32539690 http://dx.doi.org/10.1186/s12884-020-03051-2 |
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author | Soffer, Marti D. Bendapudi, Pavan K. Roberts, Drucilla J. Edelson, P. Kaitlyn Kuter, David J. Ecker, Jeffrey L. Bryant, Allison Goldfarb, Ilona T. |
author_facet | Soffer, Marti D. Bendapudi, Pavan K. Roberts, Drucilla J. Edelson, P. Kaitlyn Kuter, David J. Ecker, Jeffrey L. Bryant, Allison Goldfarb, Ilona T. |
author_sort | Soffer, Marti D. |
collection | PubMed |
description | BACKGROUND: Thrombotic thrombocytopenic purpura (TTP) is a rare but serious complication in pregnancy that places the mother and fetus at high risk for morbidity and mortality. This case illustrates novel pregnancy complications associated with this rare medical condition. CASE PRESENTATION: A 31-year-old G3P0020 at 28 weeks and 1 day was admitted with severe thrombocytopenia and was ultimately diagnosed with TTP. With therapeutic plasma exchange (TPE), maternal status improved. At 28 weeks 6 days, however, non-reassuring fetal testing prompted cesarean delivery with placental abruption noted intraoperatively. Pathology examination confirmed placental abruption and also revealed multiple placental infarcts. CONCLUSION: While medical management of TTP can significantly improve the health of the mother, this case highlights the potential role of TTP in abruption and other placental pathology and thus, the need for close fetal surveillance throughout an affected pregnancy. |
format | Online Article Text |
id | pubmed-7296940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72969402020-06-16 Congenital thrombotic thrombocytopenic purpura (TTP) with placental abruption despite maternal improvement: a case report Soffer, Marti D. Bendapudi, Pavan K. Roberts, Drucilla J. Edelson, P. Kaitlyn Kuter, David J. Ecker, Jeffrey L. Bryant, Allison Goldfarb, Ilona T. BMC Pregnancy Childbirth Case Report BACKGROUND: Thrombotic thrombocytopenic purpura (TTP) is a rare but serious complication in pregnancy that places the mother and fetus at high risk for morbidity and mortality. This case illustrates novel pregnancy complications associated with this rare medical condition. CASE PRESENTATION: A 31-year-old G3P0020 at 28 weeks and 1 day was admitted with severe thrombocytopenia and was ultimately diagnosed with TTP. With therapeutic plasma exchange (TPE), maternal status improved. At 28 weeks 6 days, however, non-reassuring fetal testing prompted cesarean delivery with placental abruption noted intraoperatively. Pathology examination confirmed placental abruption and also revealed multiple placental infarcts. CONCLUSION: While medical management of TTP can significantly improve the health of the mother, this case highlights the potential role of TTP in abruption and other placental pathology and thus, the need for close fetal surveillance throughout an affected pregnancy. BioMed Central 2020-06-15 /pmc/articles/PMC7296940/ /pubmed/32539690 http://dx.doi.org/10.1186/s12884-020-03051-2 Text en © The Author(s) 2020 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 Soffer, Marti D. Bendapudi, Pavan K. Roberts, Drucilla J. Edelson, P. Kaitlyn Kuter, David J. Ecker, Jeffrey L. Bryant, Allison Goldfarb, Ilona T. Congenital thrombotic thrombocytopenic purpura (TTP) with placental abruption despite maternal improvement: a case report |
title | Congenital thrombotic thrombocytopenic purpura (TTP) with placental abruption despite maternal improvement: a case report |
title_full | Congenital thrombotic thrombocytopenic purpura (TTP) with placental abruption despite maternal improvement: a case report |
title_fullStr | Congenital thrombotic thrombocytopenic purpura (TTP) with placental abruption despite maternal improvement: a case report |
title_full_unstemmed | Congenital thrombotic thrombocytopenic purpura (TTP) with placental abruption despite maternal improvement: a case report |
title_short | Congenital thrombotic thrombocytopenic purpura (TTP) with placental abruption despite maternal improvement: a case report |
title_sort | congenital thrombotic thrombocytopenic purpura (ttp) with placental abruption despite maternal improvement: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296940/ https://www.ncbi.nlm.nih.gov/pubmed/32539690 http://dx.doi.org/10.1186/s12884-020-03051-2 |
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