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Successful Management of Pregnancy Complicated by Klippel-Trenaunay Syndrome Using MR Angiography-Based Evaluation
Klippel-Trenaunay syndrome (KTS) is a rare congenital disease, and extensive cutaneous hemangiomas and abnormal venous vessels are characteristic. In our case, to manage her pregnancy with KTS, whole-body MRA was performed before delivery. A 29-year-old woman was referred at 28 weeks because of prom...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335629/ https://www.ncbi.nlm.nih.gov/pubmed/22567516 http://dx.doi.org/10.1155/2011/723467 |
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author | Tanaka, Reiko Fujita, Yasuyuki Ishibashi Hiasa, Kana Yumoto, Yasuo Hidaka, Nobuhiro Fukushima, Kotaro Wake, Norio |
author_facet | Tanaka, Reiko Fujita, Yasuyuki Ishibashi Hiasa, Kana Yumoto, Yasuo Hidaka, Nobuhiro Fukushima, Kotaro Wake, Norio |
author_sort | Tanaka, Reiko |
collection | PubMed |
description | Klippel-Trenaunay syndrome (KTS) is a rare congenital disease, and extensive cutaneous hemangiomas and abnormal venous vessels are characteristic. In our case, to manage her pregnancy with KTS, whole-body MRA was performed before delivery. A 29-year-old woman was referred at 28 weeks because of prominent vulvovaginal varicosities due to KTS. At 35 weeks, hypertrophy and multiple venous varicosities of her leg as well as massive vulvovaginal varicosities became prominent with a normal coagulation profile. Systematic MRAs revealed hemangiomas and varicosities in the right leg, the lower abdomen, and the pubic region, while no obvious AVM was detected around the bronchial tube and spine. We decided to deliver her baby by cesarean section at 37 weeks under general anesthesia, and a healthy baby was delivered. No blood transfusion was required. Prophylaxis against thrombosis was performed after the operation. She was discharged with her baby. Her vulvovaginal varicosities shrunk considerably one month later. |
format | Online Article Text |
id | pubmed-3335629 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-33356292012-05-07 Successful Management of Pregnancy Complicated by Klippel-Trenaunay Syndrome Using MR Angiography-Based Evaluation Tanaka, Reiko Fujita, Yasuyuki Ishibashi Hiasa, Kana Yumoto, Yasuo Hidaka, Nobuhiro Fukushima, Kotaro Wake, Norio Case Rep Obstet Gynecol Case Report Klippel-Trenaunay syndrome (KTS) is a rare congenital disease, and extensive cutaneous hemangiomas and abnormal venous vessels are characteristic. In our case, to manage her pregnancy with KTS, whole-body MRA was performed before delivery. A 29-year-old woman was referred at 28 weeks because of prominent vulvovaginal varicosities due to KTS. At 35 weeks, hypertrophy and multiple venous varicosities of her leg as well as massive vulvovaginal varicosities became prominent with a normal coagulation profile. Systematic MRAs revealed hemangiomas and varicosities in the right leg, the lower abdomen, and the pubic region, while no obvious AVM was detected around the bronchial tube and spine. We decided to deliver her baby by cesarean section at 37 weeks under general anesthesia, and a healthy baby was delivered. No blood transfusion was required. Prophylaxis against thrombosis was performed after the operation. She was discharged with her baby. Her vulvovaginal varicosities shrunk considerably one month later. Hindawi Publishing Corporation 2011 2011-10-27 /pmc/articles/PMC3335629/ /pubmed/22567516 http://dx.doi.org/10.1155/2011/723467 Text en Copyright © 2011 Reiko Tanaka et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Tanaka, Reiko Fujita, Yasuyuki Ishibashi Hiasa, Kana Yumoto, Yasuo Hidaka, Nobuhiro Fukushima, Kotaro Wake, Norio Successful Management of Pregnancy Complicated by Klippel-Trenaunay Syndrome Using MR Angiography-Based Evaluation |
title | Successful Management of Pregnancy Complicated by Klippel-Trenaunay Syndrome Using MR Angiography-Based Evaluation |
title_full | Successful Management of Pregnancy Complicated by Klippel-Trenaunay Syndrome Using MR Angiography-Based Evaluation |
title_fullStr | Successful Management of Pregnancy Complicated by Klippel-Trenaunay Syndrome Using MR Angiography-Based Evaluation |
title_full_unstemmed | Successful Management of Pregnancy Complicated by Klippel-Trenaunay Syndrome Using MR Angiography-Based Evaluation |
title_short | Successful Management of Pregnancy Complicated by Klippel-Trenaunay Syndrome Using MR Angiography-Based Evaluation |
title_sort | successful management of pregnancy complicated by klippel-trenaunay syndrome using mr angiography-based evaluation |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335629/ https://www.ncbi.nlm.nih.gov/pubmed/22567516 http://dx.doi.org/10.1155/2011/723467 |
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