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Bilateral Spontaneous Resolution of Traumatic Epidural Hematoma: A Case Report and Literature Review

Epidural hematomas (EDHs) are a neurosurgical emergency characterized by the accumulation of blood in the epidural space surrounding the dura mater. Spontaneous resolution of EDH is an exceptionally rare occurrence, with only 16 cases reported in the medical literature where resolution occurred with...

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Autores principales: Aleid, Abdulsalam, Alzahrani, Basmah S, Alameer, Murtadha H, Alhassan, Abdulsalam J, Alahmed, Ibrahim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207977/
https://www.ncbi.nlm.nih.gov/pubmed/37228352
http://dx.doi.org/10.7759/cureus.39379
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author Aleid, Abdulsalam
Alzahrani, Basmah S
Alameer, Murtadha H
Alhassan, Abdulsalam J
Alahmed, Ibrahim
author_facet Aleid, Abdulsalam
Alzahrani, Basmah S
Alameer, Murtadha H
Alhassan, Abdulsalam J
Alahmed, Ibrahim
author_sort Aleid, Abdulsalam
collection PubMed
description Epidural hematomas (EDHs) are a neurosurgical emergency characterized by the accumulation of blood in the epidural space surrounding the dura mater. Spontaneous resolution of EDH is an exceptionally rare occurrence, with only 16 cases reported in the medical literature where resolution occurred within 24 hours of onset. In this case report, we present a unique instance of a chronic EDH that spontaneously resolved over a period of seven months. This case adds to the scientific literature by highlighting an extremely prolonged duration of spontaneous EDH resolution, which, to our knowledge, has not been previously documented. A 59-year-old male suffered a head injury following a fall. He presented with a progressively worsening headache and nausea, raising concerns for a potential EDH. A computed tomography (CT) scan confirmed the presence of a large right parietal EDH measuring 58 × 23 × ​​​​​​​17 mm and a large left frontoparietal EDH measuring 90 × 20 ×​​​​​​​ 12 mm. These findings were crucial in establishing the primary diagnosis and guiding subsequent interventions. Upon diagnosis of the EDHs, the patient received conservative treatment and was closely monitored. Over a period of seven months, follow-up imaging revealed complete resolution of both EDHs, with restoration of normal midline structures and ventricular sizes. Notably, this represents the longest duration of spontaneous EDH resolution reported in the literature. We attribute this uncommon outcome to the activation of endogenous fibrinolytic pathways, which are responsible for dissolving blood clots and hematomas. In addition, the formation of new collateral blood vessels around the hematoma may help facilitate its resolution. This case underscores the significance of early recognition and vigilant monitoring of EDH cases. While immediate surgical intervention remains essential in most instances, conservative management can be considered in select cases. Our report demonstrates the possibility of spontaneous resolution of EDHs over an extended period, emphasizing the importance of continued observation and appropriate management. By shedding light on this rare occurrence, this case report contributes to the limited existing literature on the topic, providing valuable insights and adding to our understanding of EDH management.
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spelling pubmed-102079772023-05-24 Bilateral Spontaneous Resolution of Traumatic Epidural Hematoma: A Case Report and Literature Review Aleid, Abdulsalam Alzahrani, Basmah S Alameer, Murtadha H Alhassan, Abdulsalam J Alahmed, Ibrahim Cureus Neurosurgery Epidural hematomas (EDHs) are a neurosurgical emergency characterized by the accumulation of blood in the epidural space surrounding the dura mater. Spontaneous resolution of EDH is an exceptionally rare occurrence, with only 16 cases reported in the medical literature where resolution occurred within 24 hours of onset. In this case report, we present a unique instance of a chronic EDH that spontaneously resolved over a period of seven months. This case adds to the scientific literature by highlighting an extremely prolonged duration of spontaneous EDH resolution, which, to our knowledge, has not been previously documented. A 59-year-old male suffered a head injury following a fall. He presented with a progressively worsening headache and nausea, raising concerns for a potential EDH. A computed tomography (CT) scan confirmed the presence of a large right parietal EDH measuring 58 × 23 × ​​​​​​​17 mm and a large left frontoparietal EDH measuring 90 × 20 ×​​​​​​​ 12 mm. These findings were crucial in establishing the primary diagnosis and guiding subsequent interventions. Upon diagnosis of the EDHs, the patient received conservative treatment and was closely monitored. Over a period of seven months, follow-up imaging revealed complete resolution of both EDHs, with restoration of normal midline structures and ventricular sizes. Notably, this represents the longest duration of spontaneous EDH resolution reported in the literature. We attribute this uncommon outcome to the activation of endogenous fibrinolytic pathways, which are responsible for dissolving blood clots and hematomas. In addition, the formation of new collateral blood vessels around the hematoma may help facilitate its resolution. This case underscores the significance of early recognition and vigilant monitoring of EDH cases. While immediate surgical intervention remains essential in most instances, conservative management can be considered in select cases. Our report demonstrates the possibility of spontaneous resolution of EDHs over an extended period, emphasizing the importance of continued observation and appropriate management. By shedding light on this rare occurrence, this case report contributes to the limited existing literature on the topic, providing valuable insights and adding to our understanding of EDH management. Cureus 2023-05-23 /pmc/articles/PMC10207977/ /pubmed/37228352 http://dx.doi.org/10.7759/cureus.39379 Text en Copyright © 2023, Aleid et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Neurosurgery
Aleid, Abdulsalam
Alzahrani, Basmah S
Alameer, Murtadha H
Alhassan, Abdulsalam J
Alahmed, Ibrahim
Bilateral Spontaneous Resolution of Traumatic Epidural Hematoma: A Case Report and Literature Review
title Bilateral Spontaneous Resolution of Traumatic Epidural Hematoma: A Case Report and Literature Review
title_full Bilateral Spontaneous Resolution of Traumatic Epidural Hematoma: A Case Report and Literature Review
title_fullStr Bilateral Spontaneous Resolution of Traumatic Epidural Hematoma: A Case Report and Literature Review
title_full_unstemmed Bilateral Spontaneous Resolution of Traumatic Epidural Hematoma: A Case Report and Literature Review
title_short Bilateral Spontaneous Resolution of Traumatic Epidural Hematoma: A Case Report and Literature Review
title_sort bilateral spontaneous resolution of traumatic epidural hematoma: a case report and literature review
topic Neurosurgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207977/
https://www.ncbi.nlm.nih.gov/pubmed/37228352
http://dx.doi.org/10.7759/cureus.39379
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