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Traumatic subgaleal hematoma in patient with Ehlers-Danlos syndrome: A rare case report
BACKGROUND: A subgaleal hematoma (SGH) describes scalp bleeding in the potential space between the periosteum and the galea aponeurosis. This hematoma generally occurs after vacuum-assisted and forceps delivery, but may also be seen following head trauma. Despite its benign course, SGHs may complica...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282823/ https://www.ncbi.nlm.nih.gov/pubmed/35855180 http://dx.doi.org/10.25259/SNI_186_2022 |
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author | Gurses, Muhammet Enes Bahadir, Siyar Bilginer, Burcak |
author_facet | Gurses, Muhammet Enes Bahadir, Siyar Bilginer, Burcak |
author_sort | Gurses, Muhammet Enes |
collection | PubMed |
description | BACKGROUND: A subgaleal hematoma (SGH) describes scalp bleeding in the potential space between the periosteum and the galea aponeurosis. This hematoma generally occurs after vacuum-assisted and forceps delivery, but may also be seen following head trauma. Despite its benign course, SGHs may complicate by life-threatening events. CASE DESCRIPTION: We report a case of a 10-year-old male with Ehlers-Danlos syndrome presenting with scalp swelling following minor head trauma. On examination, a small swelling was observed in the occipital region. During the follow up, as the volume of subgaleal hematoma was increasing, we performed needle aspiration to achieve volume reduction, and dressed with a cap like bandage that wrapped and compressed scalp. The patient was hospitalized due to hemodynamic instability and a blood transfusion was performed. Due to extended usage of compressive bandage, a large area of scalp tissue became necrotic. The necrotic scalp tissue was debrided and reconstructed by plastic and reconstructive surgery. After surgery, another hematoma formed extending from the front of the ear to the ipsilateral neck caused facial paralysis, this hematoma was evacuated and a drain was placed. The patient was followed up for 1 year and no recurrent cephalhematoma was observed. CONCLUSION: Ehlers-Danlos is a rarely encountered connective tissue syndrome, this case underscores the importance for neurosurgery physicians to recognize the potential catastrophes, these patients may present with following even minor injury. |
format | Online Article Text |
id | pubmed-9282823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-92828232022-07-18 Traumatic subgaleal hematoma in patient with Ehlers-Danlos syndrome: A rare case report Gurses, Muhammet Enes Bahadir, Siyar Bilginer, Burcak Surg Neurol Int Case Report BACKGROUND: A subgaleal hematoma (SGH) describes scalp bleeding in the potential space between the periosteum and the galea aponeurosis. This hematoma generally occurs after vacuum-assisted and forceps delivery, but may also be seen following head trauma. Despite its benign course, SGHs may complicate by life-threatening events. CASE DESCRIPTION: We report a case of a 10-year-old male with Ehlers-Danlos syndrome presenting with scalp swelling following minor head trauma. On examination, a small swelling was observed in the occipital region. During the follow up, as the volume of subgaleal hematoma was increasing, we performed needle aspiration to achieve volume reduction, and dressed with a cap like bandage that wrapped and compressed scalp. The patient was hospitalized due to hemodynamic instability and a blood transfusion was performed. Due to extended usage of compressive bandage, a large area of scalp tissue became necrotic. The necrotic scalp tissue was debrided and reconstructed by plastic and reconstructive surgery. After surgery, another hematoma formed extending from the front of the ear to the ipsilateral neck caused facial paralysis, this hematoma was evacuated and a drain was placed. The patient was followed up for 1 year and no recurrent cephalhematoma was observed. CONCLUSION: Ehlers-Danlos is a rarely encountered connective tissue syndrome, this case underscores the importance for neurosurgery physicians to recognize the potential catastrophes, these patients may present with following even minor injury. Scientific Scholar 2022-06-23 /pmc/articles/PMC9282823/ /pubmed/35855180 http://dx.doi.org/10.25259/SNI_186_2022 Text en Copyright: © 2022 Surgical Neurology International https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Gurses, Muhammet Enes Bahadir, Siyar Bilginer, Burcak Traumatic subgaleal hematoma in patient with Ehlers-Danlos syndrome: A rare case report |
title | Traumatic subgaleal hematoma in patient with Ehlers-Danlos syndrome: A rare case report |
title_full | Traumatic subgaleal hematoma in patient with Ehlers-Danlos syndrome: A rare case report |
title_fullStr | Traumatic subgaleal hematoma in patient with Ehlers-Danlos syndrome: A rare case report |
title_full_unstemmed | Traumatic subgaleal hematoma in patient with Ehlers-Danlos syndrome: A rare case report |
title_short | Traumatic subgaleal hematoma in patient with Ehlers-Danlos syndrome: A rare case report |
title_sort | traumatic subgaleal hematoma in patient with ehlers-danlos syndrome: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282823/ https://www.ncbi.nlm.nih.gov/pubmed/35855180 http://dx.doi.org/10.25259/SNI_186_2022 |
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