Bilateral basal ganglia hemorrhage in a 2-year-old child

M. Alrawi, Muthanna N. Abdulqader, Hayder R. Salih, Saleh Abdulkareem Saleh, Mohammedbaqer Ali Al-Ghuraibawi, Mustafa M. Altaweel, M. Ismail, Samer S. Hoz
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Abstract

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. 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. Bilateral BGH is extremely rare, and to the best of our knowledge, this is the first case report in pediatric age groups.
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一名两岁儿童的双侧基底节出血
基底神经节出血(BGH)是一种位于尾状核、壳核、白球或邻近结构如丘脑或内囊的脑内出血亚型。双侧基底神经节受累极为罕见。在这里,我们报告一个2岁的女性谁被发现有自发性双侧BGH与一个独特的出血延伸。一名2岁女童表现为意识水平下降、癫痫发作和发烧,在影像学评估中发现双侧BGH,从尾状头部延伸到壳核、苍白球和内囊前肢。双侧BGH极为罕见,据我们所知,这是儿科年龄组的首例病例报告。
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CiteScore
1.30
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0.00%
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623
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