{"title":"Acute hemorrhagic leukoencephalopathy: a case report and literature review","authors":"Bassel Achmeh, Mohamad Nabil Wahbi, Huda Daood","doi":"10.1097/ms9.0000000000002353","DOIUrl":null,"url":null,"abstract":"\n \n Acute hemorrhagic leukoencephalopathy (AHLE) is a rare and devastating condition that can present with various neurological symptoms. The predisposing and initiating factors of AHLE are not fully understood. AHLE has a high morbidity and significant mortality rates, however, our case presents a surviving young girl.\n \n \n \n 13 years old previously healthy girl was referred to the emergency department due to drowsiness, preceded by an upper respiratory infection 10 days earlier. Firstly, she was treated empirical with anti viral medication (Acyclovir) directed to herpes simplex virus and intra venous ( IV) methylprednisolone pulses. When She did not respond well, intravenous immunoglobulin (IVIG) was administrated, which helped with the end-result diagnosis based on clinical and imaging findings.\n \n \n \n AHLE is a fatal rare demyelinating disease characterized by an acute rapidly progressive fulminant inflammation of the white matter, it is usually misdiagnosed due to being a diagnosis of exclusion, and the much more common other diseases, including infectious encephalitis, meningitis, fulminant multiple sclerosis, other causes of acute disseminated encephalomyelitis (ADEM). different types of CNS infiltrates, such as neutrophils in AHLE and lymphocytes in ADEM, do not support the idea of differentiating the two diseases. The process of differentiating between these two diseases relies mostly on laboratory and imaging findings, which are well demonstrated in this case report.\n \n \n \n We conclude this report by highlighting the dearth in published knowledge about this disease, and encouraging further studies be conducted about this topic.\n","PeriodicalId":503882,"journal":{"name":"Annals of Medicine & Surgery","volume":"7 12","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Medicine & Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/ms9.0000000000002353","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Acute hemorrhagic leukoencephalopathy (AHLE) is a rare and devastating condition that can present with various neurological symptoms. The predisposing and initiating factors of AHLE are not fully understood. AHLE has a high morbidity and significant mortality rates, however, our case presents a surviving young girl.
13 years old previously healthy girl was referred to the emergency department due to drowsiness, preceded by an upper respiratory infection 10 days earlier. Firstly, she was treated empirical with anti viral medication (Acyclovir) directed to herpes simplex virus and intra venous ( IV) methylprednisolone pulses. When She did not respond well, intravenous immunoglobulin (IVIG) was administrated, which helped with the end-result diagnosis based on clinical and imaging findings.
AHLE is a fatal rare demyelinating disease characterized by an acute rapidly progressive fulminant inflammation of the white matter, it is usually misdiagnosed due to being a diagnosis of exclusion, and the much more common other diseases, including infectious encephalitis, meningitis, fulminant multiple sclerosis, other causes of acute disseminated encephalomyelitis (ADEM). different types of CNS infiltrates, such as neutrophils in AHLE and lymphocytes in ADEM, do not support the idea of differentiating the two diseases. The process of differentiating between these two diseases relies mostly on laboratory and imaging findings, which are well demonstrated in this case report.
We conclude this report by highlighting the dearth in published knowledge about this disease, and encouraging further studies be conducted about this topic.