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Spontaneous Subgaleal Hematoma in a Sickle Cell Disease Patient: A Case Report
Moayad Majed Alqurashi1, Omar Muntaser Raslan2,3, Giamal Edin Gmati4,5,6
1Department of Medicine, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Abstract:
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.
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