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Fetal subdural hematoma, sickle cell disease and storage pool disease: A case report
A fetal subdural hematoma (SDH) was diagnosed in a patient with sickle cell disease (SCD) during a routine ultrasound exam in the 30th week of pregnancy. A scan performed a few days earlier had revealed no abnormalities. After interdisciplinary consultation with neurosurgeons and neonatologists, a c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057149/ https://www.ncbi.nlm.nih.gov/pubmed/32154119 http://dx.doi.org/10.1016/j.crwh.2020.e00183 |
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author | Iannaccone, Antonella Darkwah Oppong, Marvin Dammann, Philipp Kimmig, Rainer Köninger, Angela |
author_facet | Iannaccone, Antonella Darkwah Oppong, Marvin Dammann, Philipp Kimmig, Rainer Köninger, Angela |
author_sort | Iannaccone, Antonella |
collection | PubMed |
description | A fetal subdural hematoma (SDH) was diagnosed in a patient with sickle cell disease (SCD) during a routine ultrasound exam in the 30th week of pregnancy. A scan performed a few days earlier had revealed no abnormalities. After interdisciplinary consultation with neurosurgeons and neonatologists, a cesarean section was performed since acute subdural bleeding was hypothesized and the mother's condition was critical. After surgery, the diagnostic procedures revealed that the child and the mother had also suffered from thrombocytopathy, which probably jointly contributed to causing the bleeding; in general, anemia and hypoxia may also play an important role. The newborn had a good neurological outcome. Ultrasound features do not reflect the underlying cause and therefore predicting the prognosis is challenging. In most cases, prenatal counseling is difficult because of the unknown underlying cause and because there are no ultrasound or magnetic resonance imaging criteria to define which cases can benefit from delivery or expectant management. Where there is acute bleeding, the child could benefit from delivery and surgical evacuation of the hematoma. Further investigation to identify the cause of the bleeding can improve management and prognosis. |
format | Online Article Text |
id | pubmed-7057149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-70571492020-03-09 Fetal subdural hematoma, sickle cell disease and storage pool disease: A case report Iannaccone, Antonella Darkwah Oppong, Marvin Dammann, Philipp Kimmig, Rainer Köninger, Angela Case Rep Womens Health Article A fetal subdural hematoma (SDH) was diagnosed in a patient with sickle cell disease (SCD) during a routine ultrasound exam in the 30th week of pregnancy. A scan performed a few days earlier had revealed no abnormalities. After interdisciplinary consultation with neurosurgeons and neonatologists, a cesarean section was performed since acute subdural bleeding was hypothesized and the mother's condition was critical. After surgery, the diagnostic procedures revealed that the child and the mother had also suffered from thrombocytopathy, which probably jointly contributed to causing the bleeding; in general, anemia and hypoxia may also play an important role. The newborn had a good neurological outcome. Ultrasound features do not reflect the underlying cause and therefore predicting the prognosis is challenging. In most cases, prenatal counseling is difficult because of the unknown underlying cause and because there are no ultrasound or magnetic resonance imaging criteria to define which cases can benefit from delivery or expectant management. Where there is acute bleeding, the child could benefit from delivery and surgical evacuation of the hematoma. Further investigation to identify the cause of the bleeding can improve management and prognosis. Elsevier 2020-02-20 /pmc/articles/PMC7057149/ /pubmed/32154119 http://dx.doi.org/10.1016/j.crwh.2020.e00183 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Iannaccone, Antonella Darkwah Oppong, Marvin Dammann, Philipp Kimmig, Rainer Köninger, Angela Fetal subdural hematoma, sickle cell disease and storage pool disease: A case report |
title | Fetal subdural hematoma, sickle cell disease and storage pool disease: A case report |
title_full | Fetal subdural hematoma, sickle cell disease and storage pool disease: A case report |
title_fullStr | Fetal subdural hematoma, sickle cell disease and storage pool disease: A case report |
title_full_unstemmed | Fetal subdural hematoma, sickle cell disease and storage pool disease: A case report |
title_short | Fetal subdural hematoma, sickle cell disease and storage pool disease: A case report |
title_sort | fetal subdural hematoma, sickle cell disease and storage pool disease: a case report |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057149/ https://www.ncbi.nlm.nih.gov/pubmed/32154119 http://dx.doi.org/10.1016/j.crwh.2020.e00183 |
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