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Pregnancy Complicated by Gorham–Stout Disease and Refractory Chylothorax
Introduction Gorham–Stout Disease (GSD) is a rare disorder of bony destruction due to lymphangiomatosis, and is often triggered by hormones. One complication of GSD is the development of chylothorax, which carries a high mortality rate. Very little experience has been published to guide management i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Thieme Medical Publishers
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050042/ https://www.ncbi.nlm.nih.gov/pubmed/27708981 http://dx.doi.org/10.1055/s-0036-1593443 |
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author | Hellyer, Jessica Oliver-Allen, Hunter Shafiq, Majid Tolani, Alisha Druzin, Maurice Jeng, Michael Rockson, Stanley Lowsky, Robert |
author_facet | Hellyer, Jessica Oliver-Allen, Hunter Shafiq, Majid Tolani, Alisha Druzin, Maurice Jeng, Michael Rockson, Stanley Lowsky, Robert |
author_sort | Hellyer, Jessica |
collection | PubMed |
description | Introduction Gorham–Stout Disease (GSD) is a rare disorder of bony destruction due to lymphangiomatosis, and is often triggered by hormones. One complication of GSD is the development of chylothorax, which carries a high mortality rate. Very little experience has been published to guide management in GSD during pregnancy to optimize both fetal and maternal health. Case Study A 20-year-old woman with known GSD presented with shortness of breath at 18 weeks of pregnancy, due to bilateral chylothoraces which required daily drainage. To minimize chylous fluid formation, she was placed on bowel rest with total parenteral nutrition (limiting lipid intake) and received octreotide to decrease splanchnic blood flow and chylous fluid drainage. Treatment options were limited due to her pregnancy. Twice daily home chest tube drainage of a single lung cavity, total parenteral nutrition, octreotide, and albumin infusions allowed successful delivery of a healthy 37 weeks' gestation infant by cesarean delivery. Discussion This case illustrates the management of a rare clinical disease of bone resorption and lymphangiomatosis complicated by bilateral, refractory chylothoraces, triggered by pregnancy, in whom treatment options are limited, and the need for a multidisciplinary health care team to ensure successful maternal and fetal outcomes. |
format | Online Article Text |
id | pubmed-5050042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Thieme Medical Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-50500422016-10-05 Pregnancy Complicated by Gorham–Stout Disease and Refractory Chylothorax Hellyer, Jessica Oliver-Allen, Hunter Shafiq, Majid Tolani, Alisha Druzin, Maurice Jeng, Michael Rockson, Stanley Lowsky, Robert AJP Rep Introduction Gorham–Stout Disease (GSD) is a rare disorder of bony destruction due to lymphangiomatosis, and is often triggered by hormones. One complication of GSD is the development of chylothorax, which carries a high mortality rate. Very little experience has been published to guide management in GSD during pregnancy to optimize both fetal and maternal health. Case Study A 20-year-old woman with known GSD presented with shortness of breath at 18 weeks of pregnancy, due to bilateral chylothoraces which required daily drainage. To minimize chylous fluid formation, she was placed on bowel rest with total parenteral nutrition (limiting lipid intake) and received octreotide to decrease splanchnic blood flow and chylous fluid drainage. Treatment options were limited due to her pregnancy. Twice daily home chest tube drainage of a single lung cavity, total parenteral nutrition, octreotide, and albumin infusions allowed successful delivery of a healthy 37 weeks' gestation infant by cesarean delivery. Discussion This case illustrates the management of a rare clinical disease of bone resorption and lymphangiomatosis complicated by bilateral, refractory chylothoraces, triggered by pregnancy, in whom treatment options are limited, and the need for a multidisciplinary health care team to ensure successful maternal and fetal outcomes. Thieme Medical Publishers 2016-10 /pmc/articles/PMC5050042/ /pubmed/27708981 http://dx.doi.org/10.1055/s-0036-1593443 Text en © Thieme Medical Publishers |
spellingShingle | Hellyer, Jessica Oliver-Allen, Hunter Shafiq, Majid Tolani, Alisha Druzin, Maurice Jeng, Michael Rockson, Stanley Lowsky, Robert Pregnancy Complicated by Gorham–Stout Disease and Refractory Chylothorax |
title | Pregnancy Complicated by Gorham–Stout Disease and Refractory Chylothorax |
title_full | Pregnancy Complicated by Gorham–Stout Disease and Refractory Chylothorax |
title_fullStr | Pregnancy Complicated by Gorham–Stout Disease and Refractory Chylothorax |
title_full_unstemmed | Pregnancy Complicated by Gorham–Stout Disease and Refractory Chylothorax |
title_short | Pregnancy Complicated by Gorham–Stout Disease and Refractory Chylothorax |
title_sort | pregnancy complicated by gorham–stout disease and refractory chylothorax |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050042/ https://www.ncbi.nlm.nih.gov/pubmed/27708981 http://dx.doi.org/10.1055/s-0036-1593443 |
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