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Spontaneous Subgaleal Hematoma in a Sickle Cell Disease Patient: A Case Report
Sickle cell disease (SCD) is one of the most commonly inherited conditions on the Arabian Peninsula. We report a case of a 17-year-old boy, who had previously been diagnosed with SCD and glucose-6-phosphate dehydrogenase (G6PD) deficiency and recently presented to our hospital with spontaneous subga...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elmer Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383627/ https://www.ncbi.nlm.nih.gov/pubmed/34434360 http://dx.doi.org/10.14740/jmc3433 |
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author | Alqurashi, Moayad Majed Raslan, Omar Muntaser Gmati, Giamal Edin |
author_facet | Alqurashi, Moayad Majed Raslan, Omar Muntaser Gmati, Giamal Edin |
author_sort | Alqurashi, Moayad Majed |
collection | PubMed |
description | Sickle cell disease (SCD) is one of the most commonly inherited conditions on the Arabian Peninsula. We report a case of a 17-year-old boy, who had previously been diagnosed with SCD and glucose-6-phosphate dehydrogenase (G6PD) deficiency and recently presented to our hospital with spontaneous subgaleal hematoma (SGH), which was managed conservatively. We also present a literature review on the topic of spontaneous intra- and/or extra-cranial bleeds. |
format | Online Article Text |
id | pubmed-8383627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elmer Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-83836272021-08-24 Spontaneous Subgaleal Hematoma in a Sickle Cell Disease Patient: A Case Report Alqurashi, Moayad Majed Raslan, Omar Muntaser Gmati, Giamal Edin J Med Cases Case Report Sickle cell disease (SCD) is one of the most commonly inherited conditions on the Arabian Peninsula. We report a case of a 17-year-old boy, who had previously been diagnosed with SCD and glucose-6-phosphate dehydrogenase (G6PD) deficiency and recently presented to our hospital with spontaneous subgaleal hematoma (SGH), which was managed conservatively. We also present a literature review on the topic of spontaneous intra- and/or extra-cranial bleeds. Elmer Press 2020-02 2020-02-28 /pmc/articles/PMC8383627/ /pubmed/34434360 http://dx.doi.org/10.14740/jmc3433 Text en Copyright 2020, Alqurashi et al. https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Alqurashi, Moayad Majed Raslan, Omar Muntaser Gmati, Giamal Edin Spontaneous Subgaleal Hematoma in a Sickle Cell Disease Patient: A Case Report |
title | Spontaneous Subgaleal Hematoma in a Sickle Cell Disease Patient: A Case Report |
title_full | Spontaneous Subgaleal Hematoma in a Sickle Cell Disease Patient: A Case Report |
title_fullStr | Spontaneous Subgaleal Hematoma in a Sickle Cell Disease Patient: A Case Report |
title_full_unstemmed | Spontaneous Subgaleal Hematoma in a Sickle Cell Disease Patient: A Case Report |
title_short | Spontaneous Subgaleal Hematoma in a Sickle Cell Disease Patient: A Case Report |
title_sort | spontaneous subgaleal hematoma in a sickle cell disease patient: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383627/ https://www.ncbi.nlm.nih.gov/pubmed/34434360 http://dx.doi.org/10.14740/jmc3433 |
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