M. Alrawi, Muthanna N. Abdulqader, Hayder R. Salih, Saleh Abdulkareem Saleh, Mohammedbaqer Ali Al-Ghuraibawi, Mustafa M. Altaweel, M. Ismail, Samer S. Hoz
{"title":"一名两岁儿童的双侧基底节出血","authors":"M. Alrawi, Muthanna N. Abdulqader, Hayder R. Salih, Saleh Abdulkareem Saleh, Mohammedbaqer Ali Al-Ghuraibawi, Mustafa M. Altaweel, M. Ismail, Samer S. Hoz","doi":"10.25259/sni_973_2022","DOIUrl":null,"url":null,"abstract":"\n\nBasal 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.\n\n\n\nA 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.\n\n\n\nBilateral BGH is extremely rare, and to the best of our knowledge, this is the first case report in pediatric age groups.\n","PeriodicalId":38981,"journal":{"name":"Surgical Neurology International","volume":"3 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bilateral basal ganglia hemorrhage in a 2-year-old child\",\"authors\":\"M. Alrawi, Muthanna N. Abdulqader, Hayder R. Salih, Saleh Abdulkareem Saleh, Mohammedbaqer Ali Al-Ghuraibawi, Mustafa M. Altaweel, M. Ismail, Samer S. Hoz\",\"doi\":\"10.25259/sni_973_2022\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n\\nBasal 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.\\n\\n\\n\\nA 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.\\n\\n\\n\\nBilateral BGH is extremely rare, and to the best of our knowledge, this is the first case report in pediatric age groups.\\n\",\"PeriodicalId\":38981,\"journal\":{\"name\":\"Surgical Neurology International\",\"volume\":\"3 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Surgical Neurology International\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.25259/sni_973_2022\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Surgical Neurology International","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.25259/sni_973_2022","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
Bilateral basal ganglia hemorrhage in a 2-year-old child
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.