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Fetal axillary cystic hygroma detected by prenatal ultrasonography: a case report.
Fetal cystic hygroma is a rare developmental congenital anomaly of the lymphatic system, characterized by the formation of a multilocular, variable sized cystic mass. Most of cystic hygromas are found in the neck and other rare locations include axilla, mediastinum, and limbs. There are many papers...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Korean Academy of Medical Sciences
2002
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054879/ https://www.ncbi.nlm.nih.gov/pubmed/12068147 |
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author | Song, Tae-Bok Kim, Cheol-Hong Kim, Seok-Mo Kim, Yoon-Ha Byun, Ji-Soo Kim, Eun-Kyung |
author_facet | Song, Tae-Bok Kim, Cheol-Hong Kim, Seok-Mo Kim, Yoon-Ha Byun, Ji-Soo Kim, Eun-Kyung |
author_sort | Song, Tae-Bok |
collection | PubMed |
description | Fetal cystic hygroma is a rare developmental congenital anomaly of the lymphatic system, characterized by the formation of a multilocular, variable sized cystic mass. Most of cystic hygromas are found in the neck and other rare locations include axilla, mediastinum, and limbs. There are many papers about cystic hygroma colli, but there are only a few papers about fetal axillary cystic hygroma and no domestic papers. We present a case of fetal axillary cystic hygroma diagnosed antenatally followed by full-term delivery in a 30-yr-old woman. Operation was performed on the 8th day after birth and the mass was excised and confirmed as cystic hygroma. |
format | Text |
id | pubmed-3054879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-30548792011-03-15 Fetal axillary cystic hygroma detected by prenatal ultrasonography: a case report. Song, Tae-Bok Kim, Cheol-Hong Kim, Seok-Mo Kim, Yoon-Ha Byun, Ji-Soo Kim, Eun-Kyung J Korean Med Sci Research Article Fetal cystic hygroma is a rare developmental congenital anomaly of the lymphatic system, characterized by the formation of a multilocular, variable sized cystic mass. Most of cystic hygromas are found in the neck and other rare locations include axilla, mediastinum, and limbs. There are many papers about cystic hygroma colli, but there are only a few papers about fetal axillary cystic hygroma and no domestic papers. We present a case of fetal axillary cystic hygroma diagnosed antenatally followed by full-term delivery in a 30-yr-old woman. Operation was performed on the 8th day after birth and the mass was excised and confirmed as cystic hygroma. Korean Academy of Medical Sciences 2002-06 /pmc/articles/PMC3054879/ /pubmed/12068147 Text en |
spellingShingle | Research Article Song, Tae-Bok Kim, Cheol-Hong Kim, Seok-Mo Kim, Yoon-Ha Byun, Ji-Soo Kim, Eun-Kyung Fetal axillary cystic hygroma detected by prenatal ultrasonography: a case report. |
title | Fetal axillary cystic hygroma detected by prenatal ultrasonography: a case report. |
title_full | Fetal axillary cystic hygroma detected by prenatal ultrasonography: a case report. |
title_fullStr | Fetal axillary cystic hygroma detected by prenatal ultrasonography: a case report. |
title_full_unstemmed | Fetal axillary cystic hygroma detected by prenatal ultrasonography: a case report. |
title_short | Fetal axillary cystic hygroma detected by prenatal ultrasonography: a case report. |
title_sort | fetal axillary cystic hygroma detected by prenatal ultrasonography: a case report. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054879/ https://www.ncbi.nlm.nih.gov/pubmed/12068147 |
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