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Placental Mesenchymal Dysplasia With Normal Fetus: A Rare Case Report

Placental mesenchymal dysplasia (PMD) is a rare benign placental abnormality. It is characterized by hydropic degeneration of stem villi, placentomegaly, and increased maternal serum alpha-fetoprotein (AFP). It can be associated with different congenital abnormalities, karyotype abnormalities, and f...

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Autores principales: Pal, Subrata, Bose, Kingshuk, Ch Mondal, Prabhat, Chakrabarti, Srabani, Sikder, Mrinal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Society of Pathology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835383/
https://www.ncbi.nlm.nih.gov/pubmed/29531560
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author Pal, Subrata
Bose, Kingshuk
Ch Mondal, Prabhat
Chakrabarti, Srabani
Sikder, Mrinal
author_facet Pal, Subrata
Bose, Kingshuk
Ch Mondal, Prabhat
Chakrabarti, Srabani
Sikder, Mrinal
author_sort Pal, Subrata
collection PubMed
description Placental mesenchymal dysplasia (PMD) is a rare benign placental abnormality. It is characterized by hydropic degeneration of stem villi, placentomegaly, and increased maternal serum alpha-fetoprotein (AFP). It can be associated with different congenital abnormalities, karyotype abnormalities, and feto-maternal morbidities. It is difficult to differentiate PMDfrom partial mole, complete mole with twin pregnancy in ultrasound, and in macroscopic examination. The current paper presentsa rare case of placental mesenchymal dysplasia in a young primigravida mother who delivered a normal fetus withnormal karyotype.
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spelling pubmed-58353832018-03-12 Placental Mesenchymal Dysplasia With Normal Fetus: A Rare Case Report Pal, Subrata Bose, Kingshuk Ch Mondal, Prabhat Chakrabarti, Srabani Sikder, Mrinal Iran J Pathol Case Report Placental mesenchymal dysplasia (PMD) is a rare benign placental abnormality. It is characterized by hydropic degeneration of stem villi, placentomegaly, and increased maternal serum alpha-fetoprotein (AFP). It can be associated with different congenital abnormalities, karyotype abnormalities, and feto-maternal morbidities. It is difficult to differentiate PMDfrom partial mole, complete mole with twin pregnancy in ultrasound, and in macroscopic examination. The current paper presentsa rare case of placental mesenchymal dysplasia in a young primigravida mother who delivered a normal fetus withnormal karyotype. Iranian Society of Pathology 2017 2017-07-01 /pmc/articles/PMC5835383/ /pubmed/29531560 Text en © 2017, IRANIAN JOURNAL OF PATHOLOGY. This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Pal, Subrata
Bose, Kingshuk
Ch Mondal, Prabhat
Chakrabarti, Srabani
Sikder, Mrinal
Placental Mesenchymal Dysplasia With Normal Fetus: A Rare Case Report
title Placental Mesenchymal Dysplasia With Normal Fetus: A Rare Case Report
title_full Placental Mesenchymal Dysplasia With Normal Fetus: A Rare Case Report
title_fullStr Placental Mesenchymal Dysplasia With Normal Fetus: A Rare Case Report
title_full_unstemmed Placental Mesenchymal Dysplasia With Normal Fetus: A Rare Case Report
title_short Placental Mesenchymal Dysplasia With Normal Fetus: A Rare Case Report
title_sort placental mesenchymal dysplasia with normal fetus: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835383/
https://www.ncbi.nlm.nih.gov/pubmed/29531560
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