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Subgaleal hematoma evacuation in a pediatric patient: A case report and review of the literature

BACKGROUND: Subgaleal hematoma (SGH) is generally documented within the neonatal period and is rarely reported as a result of trauma or hair braiding in children. While rare, complications of SGH can result in ophthalmoplegia, proptosis, visual deficit, and corneal ulceration secondary to hematoma e...

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Autores principales: Patchana, Tye, Ghanchi, Hammad, Taka, Taha, Calayag, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468241/
https://www.ncbi.nlm.nih.gov/pubmed/32905325
http://dx.doi.org/10.25259/SNI_207_2020
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author Patchana, Tye
Ghanchi, Hammad
Taka, Taha
Calayag, Mark
author_facet Patchana, Tye
Ghanchi, Hammad
Taka, Taha
Calayag, Mark
author_sort Patchana, Tye
collection PubMed
description BACKGROUND: Subgaleal hematoma (SGH) is generally documented within the neonatal period and is rarely reported as a result of trauma or hair braiding in children. While rare, complications of SGH can result in ophthalmoplegia, proptosis, visual deficit, and corneal ulceration secondary to hematoma extension into the orbit. Although conservative treatment is preferential, expanding SGH should be aspirated to reduce complications associated with further expansion. CASE DESCRIPTION: A 12-year-old African-American female with no recent history of trauma presented with a chief complaint of headache along with a 2-day history of enlarging 2–3 cm ballotable bilateral frontal mass. Hematological workup was negative. The patient’s family confirmed a long history of hair braiding. The patient was initially prescribed a period of observation but returned 1-week later with enlarging SGH, necessitating surgical aspiration. CONCLUSION: SGH is rare past the neonatal period, but can be found in pediatric and adolescent patients secondary to trauma or hair pulling. Standard workup includes evaluation of the patient’s hematological profile for bleeding or coagulation deficits, as well as evaluation for child abuse. Although most cases of SGH resolve spontaneously over the course of several weeks, close follow-up is recommended. The authors present a case of a 12-year-old female presenting with enlarging subgaleal hemorrhages who underwent surgical aspiration and drainage without recurrence. A literature review was also conducted with 32 pediatric cases identified, 20 of which were related to hair pulling, combing, or braiding. We review the clinical course, imaging characteristics, surgical management, as well as a review of the literature involving subgaleal hemorrhage in pediatric patients and hair pulling.
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spelling pubmed-74682412020-09-03 Subgaleal hematoma evacuation in a pediatric patient: A case report and review of the literature Patchana, Tye Ghanchi, Hammad Taka, Taha Calayag, Mark Surg Neurol Int Case Report BACKGROUND: Subgaleal hematoma (SGH) is generally documented within the neonatal period and is rarely reported as a result of trauma or hair braiding in children. While rare, complications of SGH can result in ophthalmoplegia, proptosis, visual deficit, and corneal ulceration secondary to hematoma extension into the orbit. Although conservative treatment is preferential, expanding SGH should be aspirated to reduce complications associated with further expansion. CASE DESCRIPTION: A 12-year-old African-American female with no recent history of trauma presented with a chief complaint of headache along with a 2-day history of enlarging 2–3 cm ballotable bilateral frontal mass. Hematological workup was negative. The patient’s family confirmed a long history of hair braiding. The patient was initially prescribed a period of observation but returned 1-week later with enlarging SGH, necessitating surgical aspiration. CONCLUSION: SGH is rare past the neonatal period, but can be found in pediatric and adolescent patients secondary to trauma or hair pulling. Standard workup includes evaluation of the patient’s hematological profile for bleeding or coagulation deficits, as well as evaluation for child abuse. Although most cases of SGH resolve spontaneously over the course of several weeks, close follow-up is recommended. The authors present a case of a 12-year-old female presenting with enlarging subgaleal hemorrhages who underwent surgical aspiration and drainage without recurrence. A literature review was also conducted with 32 pediatric cases identified, 20 of which were related to hair pulling, combing, or braiding. We review the clinical course, imaging characteristics, surgical management, as well as a review of the literature involving subgaleal hemorrhage in pediatric patients and hair pulling. Scientific Scholar 2020-08-15 /pmc/articles/PMC7468241/ /pubmed/32905325 http://dx.doi.org/10.25259/SNI_207_2020 Text en Copyright: © 2020 Surgical Neurology International http://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, tweak, 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
Patchana, Tye
Ghanchi, Hammad
Taka, Taha
Calayag, Mark
Subgaleal hematoma evacuation in a pediatric patient: A case report and review of the literature
title Subgaleal hematoma evacuation in a pediatric patient: A case report and review of the literature
title_full Subgaleal hematoma evacuation in a pediatric patient: A case report and review of the literature
title_fullStr Subgaleal hematoma evacuation in a pediatric patient: A case report and review of the literature
title_full_unstemmed Subgaleal hematoma evacuation in a pediatric patient: A case report and review of the literature
title_short Subgaleal hematoma evacuation in a pediatric patient: A case report and review of the literature
title_sort subgaleal hematoma evacuation in a pediatric patient: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468241/
https://www.ncbi.nlm.nih.gov/pubmed/32905325
http://dx.doi.org/10.25259/SNI_207_2020
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