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Evaluation of placental vascularization in thrombophilia and intrauterine growth restriction (IUGR)

The placenta is an essential organ in the proper development of pregnancy, and it can present a lot of structural and vascular lesions that can affect fetal development. One of the pathologies associated with pregnancy, which can change the placental structure is thrombophilia (TPh), and this can be...

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Autores principales: Voicu, Nicoleta-Loredana, Bohîlţea, Roxana Elena, Berceanu, Sabina, Busuioc, Cristina Jana, Roşu, Gabriela-Camelia, Paitici, Ştefan, Istrate-Ofiţeru, Anca-Maria, Berceanu, Costin, Diţescu, Damian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864309/
https://www.ncbi.nlm.nih.gov/pubmed/33544798
http://dx.doi.org/10.47162/RJME.61.2.16
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author Voicu, Nicoleta-Loredana
Bohîlţea, Roxana Elena
Berceanu, Sabina
Busuioc, Cristina Jana
Roşu, Gabriela-Camelia
Paitici, Ştefan
Istrate-Ofiţeru, Anca-Maria
Berceanu, Costin
Diţescu, Damian
author_facet Voicu, Nicoleta-Loredana
Bohîlţea, Roxana Elena
Berceanu, Sabina
Busuioc, Cristina Jana
Roşu, Gabriela-Camelia
Paitici, Ştefan
Istrate-Ofiţeru, Anca-Maria
Berceanu, Costin
Diţescu, Damian
author_sort Voicu, Nicoleta-Loredana
collection PubMed
description The placenta is an essential organ in the proper development of pregnancy, and it can present a lot of structural and vascular lesions that can affect fetal development. One of the pathologies associated with pregnancy, which can change the placental structure is thrombophilia (TPh), and this can be correlated with an intrauterine growth restriction (IUGR) of the fetus. Maternal clinical aspects (age, weight) can be correlated with fetal ones (weight, gender), but also with the structural and vascular aspect of the placenta. The placental structure associated with TPh and IUGR shows macroscopic changes, such as fibrin deposition, calcifications and placental infarctions, but microscopic lesions are best highlighted by classical staining techniques: Hematoxylin–Eosin (HE), Masson’s trichrome (MT) and Periodic Acid–Schiff (PAS)–Hematoxylin, but also by immunohistochemistry technique with the help of anti-cluster of differentiation 34 (CD34) antibody that could make it possible to quantify vascular density depending on the pathology. Microscopic changes were massive infarcts caused by vascular ischemia, intravenous and extravillous fibrin deposits, calcifications, and vascular thrombosis. All these clinical, morphological and morphopathological data are interconnected and may vary in the presence of TPh and IUGR.
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spelling pubmed-78643092021-02-08 Evaluation of placental vascularization in thrombophilia and intrauterine growth restriction (IUGR) Voicu, Nicoleta-Loredana Bohîlţea, Roxana Elena Berceanu, Sabina Busuioc, Cristina Jana Roşu, Gabriela-Camelia Paitici, Ştefan Istrate-Ofiţeru, Anca-Maria Berceanu, Costin Diţescu, Damian Rom J Morphol Embryol Original Paper The placenta is an essential organ in the proper development of pregnancy, and it can present a lot of structural and vascular lesions that can affect fetal development. One of the pathologies associated with pregnancy, which can change the placental structure is thrombophilia (TPh), and this can be correlated with an intrauterine growth restriction (IUGR) of the fetus. Maternal clinical aspects (age, weight) can be correlated with fetal ones (weight, gender), but also with the structural and vascular aspect of the placenta. The placental structure associated with TPh and IUGR shows macroscopic changes, such as fibrin deposition, calcifications and placental infarctions, but microscopic lesions are best highlighted by classical staining techniques: Hematoxylin–Eosin (HE), Masson’s trichrome (MT) and Periodic Acid–Schiff (PAS)–Hematoxylin, but also by immunohistochemistry technique with the help of anti-cluster of differentiation 34 (CD34) antibody that could make it possible to quantify vascular density depending on the pathology. Microscopic changes were massive infarcts caused by vascular ischemia, intravenous and extravillous fibrin deposits, calcifications, and vascular thrombosis. All these clinical, morphological and morphopathological data are interconnected and may vary in the presence of TPh and IUGR. Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest 2020 2020-09-17 /pmc/articles/PMC7864309/ /pubmed/33544798 http://dx.doi.org/10.47162/RJME.61.2.16 Text en Copyright © 2020, Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an open-access article distributed under the terms of a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Public License, which permits unrestricted use, adaptation, distribution and reproduction in any medium, non-commercially, provided the new creations are licensed under identical terms as the original work and the original work is properly cited.
spellingShingle Original Paper
Voicu, Nicoleta-Loredana
Bohîlţea, Roxana Elena
Berceanu, Sabina
Busuioc, Cristina Jana
Roşu, Gabriela-Camelia
Paitici, Ştefan
Istrate-Ofiţeru, Anca-Maria
Berceanu, Costin
Diţescu, Damian
Evaluation of placental vascularization in thrombophilia and intrauterine growth restriction (IUGR)
title Evaluation of placental vascularization in thrombophilia and intrauterine growth restriction (IUGR)
title_full Evaluation of placental vascularization in thrombophilia and intrauterine growth restriction (IUGR)
title_fullStr Evaluation of placental vascularization in thrombophilia and intrauterine growth restriction (IUGR)
title_full_unstemmed Evaluation of placental vascularization in thrombophilia and intrauterine growth restriction (IUGR)
title_short Evaluation of placental vascularization in thrombophilia and intrauterine growth restriction (IUGR)
title_sort evaluation of placental vascularization in thrombophilia and intrauterine growth restriction (iugr)
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864309/
https://www.ncbi.nlm.nih.gov/pubmed/33544798
http://dx.doi.org/10.47162/RJME.61.2.16
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