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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Iranian Society of Pathology
2017
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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. |
format | Online Article Text |
id | pubmed-5835383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Iranian Society of Pathology |
record_format | MEDLINE/PubMed |
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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