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Spontaneous subgaleal hematoma in a patient with sickle cell disease: A case report and literature review
Sickle cell disease (SCD) is a common hemoglobin disorder with variable clinical manifestations. Spontaneous subgaleal hematoma is rare, with sporadic cases reported in patients with SCD. Most cases resolve with conservative measures. Skull bone infarction should be considered a possible cause of se...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878059/ https://www.ncbi.nlm.nih.gov/pubmed/31788283 http://dx.doi.org/10.1002/ccr3.2435 |
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author | Foula, Mohammed S. Hassan, Ali AlQurashi, Ahmed Alsaihati, Amna Sharroufna, Mohammed |
author_facet | Foula, Mohammed S. Hassan, Ali AlQurashi, Ahmed Alsaihati, Amna Sharroufna, Mohammed |
author_sort | Foula, Mohammed S. |
collection | PubMed |
description | Sickle cell disease (SCD) is a common hemoglobin disorder with variable clinical manifestations. Spontaneous subgaleal hematoma is rare, with sporadic cases reported in patients with SCD. Most cases resolve with conservative measures. Skull bone infarction should be considered a possible cause of severe acute headache in patients with SCD. |
format | Online Article Text |
id | pubmed-6878059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68780592019-11-29 Spontaneous subgaleal hematoma in a patient with sickle cell disease: A case report and literature review Foula, Mohammed S. Hassan, Ali AlQurashi, Ahmed Alsaihati, Amna Sharroufna, Mohammed Clin Case Rep Case Reports Sickle cell disease (SCD) is a common hemoglobin disorder with variable clinical manifestations. Spontaneous subgaleal hematoma is rare, with sporadic cases reported in patients with SCD. Most cases resolve with conservative measures. Skull bone infarction should be considered a possible cause of severe acute headache in patients with SCD. John Wiley and Sons Inc. 2019-10-09 /pmc/articles/PMC6878059/ /pubmed/31788283 http://dx.doi.org/10.1002/ccr3.2435 Text en © 2019 King Fahd Hospital of the University. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Case Reports Foula, Mohammed S. Hassan, Ali AlQurashi, Ahmed Alsaihati, Amna Sharroufna, Mohammed Spontaneous subgaleal hematoma in a patient with sickle cell disease: A case report and literature review |
title | Spontaneous subgaleal hematoma in a patient with sickle cell disease: A case report and literature review |
title_full | Spontaneous subgaleal hematoma in a patient with sickle cell disease: A case report and literature review |
title_fullStr | Spontaneous subgaleal hematoma in a patient with sickle cell disease: A case report and literature review |
title_full_unstemmed | Spontaneous subgaleal hematoma in a patient with sickle cell disease: A case report and literature review |
title_short | Spontaneous subgaleal hematoma in a patient with sickle cell disease: A case report and literature review |
title_sort | spontaneous subgaleal hematoma in a patient with sickle cell disease: a case report and literature review |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878059/ https://www.ncbi.nlm.nih.gov/pubmed/31788283 http://dx.doi.org/10.1002/ccr3.2435 |
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