Bilateral basal ganglia hemorrhage in a 2-year-old child.
Autor: | Alrawi MA; Department of Neurosurgery, Neurosurgery Teaching Hospital, Baghdad, Iraq., Abdulqader MN; Department of Neurosurgery, Neurosurgery Teaching Hospital, Baghdad, Iraq., Salih HR; Department of Neurosurgery, Neurosurgery Teaching Hospital, Baghdad, Iraq., Saleh SA; Department of Neurosurgery, College of Medicine, University of Baghdad, Baghdad, Iraq., Al-Ghuraibawi MA; Department of Neurosurgery, College of Medicine, University of Warith Al-Anbiyaa, Karbala, Iraq., Altaweel MM; Department of Neurosurgery, Neurosurgery Teaching Hospital, Baghdad, Iraq., Ismail M; Department of Neurosurgery, Neurosurgery Teaching Hospital, Baghdad, Iraq., Hoz SS; Department of Neurosurgery, University of Cincinnati, Cincinnati, Ohio, United States. |
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Jazyk: | angličtina |
Zdroj: | Surgical neurology international [Surg Neurol Int] 2023 Dec 01; Vol. 14, pp. 415. Date of Electronic Publication: 2023 Dec 01 (Print Publication: 2023). |
DOI: | 10.25259/SNI_973_2022 |
Abstrakt: | Background: Basal ganglia hemorrhage (BGH) is an intracerebral subtype of hemorrhage located in the caudate nucleus, putamen, globus pallidus, or adjacent structures such as the thalamus or internal capsule. Bilateral involvement of both basal ganglia is exceedingly infrequent. Herein, we report a case of a 2-year-old female who was discovered to have spontaneous bilateral BGH with a unique hemorrhagic extension. Case Description: A 2-year-old female child who presented with a decreased level of consciousness, seizure, and fever was discovered to have bilateral BGH during imaging evaluation that extended from the head of the caudate to involve the putamen, globus pallidus, and anterior limb of the internal capsule. Conclusion: Bilateral BGH is extremely rare, and to the best of our knowledge, this is the first case report in pediatric age groups. Competing Interests: There are no conflicts of interest (Copyright: © 2023 Surgical Neurology International.) |
Databáze: | MEDLINE |
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