A Case of Recurrent Hemorrhages due to a Chronic Expanding Encapsulated Intracranial Hematoma

Few case reports of encapsulated intracranial hematoma (EIH) exist, and the mechanisms underlying the onset and enlargement of EIH remain unclear. Here, we report on a 39-year-old woman with an EIH that repeatedly hemorrhaged and swelled and was ultimately surgically removed. In June 2012, the patie...

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Main Authors: Akiko Marutani, Kiyoshi Nagata, Jun Deguchi, Yuji Nikaido, Syuji Kazuki
Format: Article
Language:English
Published: Karger Publishers 2015-09-01
Series:Case Reports in Neurology
Subjects:
Online Access:http://www.karger.com/Article/FullText/440610
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spelling doaj-aa0f1c2f4a4b4ab5a0ee5e4076dcafbf2020-11-24T22:39:34ZengKarger PublishersCase Reports in Neurology1662-680X2015-09-017317318010.1159/000440610440610A Case of Recurrent Hemorrhages due to a Chronic Expanding Encapsulated Intracranial HematomaAkiko MarutaniKiyoshi NagataJun DeguchiYuji NikaidoSyuji KazukiFew case reports of encapsulated intracranial hematoma (EIH) exist, and the mechanisms underlying the onset and enlargement of EIH remain unclear. Here, we report on a 39-year-old woman with an EIH that repeatedly hemorrhaged and swelled and was ultimately surgically removed. In June 2012, the patient visited her local doctor, complaining of headaches. A magnetic resonance imaging (MRI) scan identified a small hemorrhage of approximately 7 mm in her right basal ganglia, and a wait-and-see approach was adopted. Six months later, her headaches recurred. She was admitted to our department after MRI showed tumor lesions accompanying the intermittent hemorrhaging in the right basal ganglia. After admission, hemorrhaging was again observed, with symptoms progressing to left-sided hemiplegia and fluctuating consciousness; thus, a craniotomy was performed. No obvious abnormal blood vessels were observed on the preoperative cerebral angiography. We accessed the lesion using a transcortical approach via a right frontotemporal craniotomy and removed the subacute hematoma by extracting the encapsulated tumor as a single mass. Subsequent pathological examinations showed that the hematoma exhibited abnormal internal vascularization and was covered with a capsule formed from growing capillaries and accumulating collagen fibers, suggesting that it was an EIH. No lingering neurological symptoms were noted upon postoperative follow-up. This type of hematoma expands slowly and is asymptomatic, with reported cases consisting of patients that already have neurological deficits due to progressive hematoma growth. Our report is one of a few to provide a clinical picture of the initial stages that occur prior to hematoma encapsulation.http://www.karger.com/Article/FullText/440610Encapsulated intracranial hematomaFibrous capsuleAngiographically occult intracranial vascular malformationChronic encapsulated hematoma
collection DOAJ
language English
format Article
sources DOAJ
author Akiko Marutani
Kiyoshi Nagata
Jun Deguchi
Yuji Nikaido
Syuji Kazuki
spellingShingle Akiko Marutani
Kiyoshi Nagata
Jun Deguchi
Yuji Nikaido
Syuji Kazuki
A Case of Recurrent Hemorrhages due to a Chronic Expanding Encapsulated Intracranial Hematoma
Case Reports in Neurology
Encapsulated intracranial hematoma
Fibrous capsule
Angiographically occult intracranial vascular malformation
Chronic encapsulated hematoma
author_facet Akiko Marutani
Kiyoshi Nagata
Jun Deguchi
Yuji Nikaido
Syuji Kazuki
author_sort Akiko Marutani
title A Case of Recurrent Hemorrhages due to a Chronic Expanding Encapsulated Intracranial Hematoma
title_short A Case of Recurrent Hemorrhages due to a Chronic Expanding Encapsulated Intracranial Hematoma
title_full A Case of Recurrent Hemorrhages due to a Chronic Expanding Encapsulated Intracranial Hematoma
title_fullStr A Case of Recurrent Hemorrhages due to a Chronic Expanding Encapsulated Intracranial Hematoma
title_full_unstemmed A Case of Recurrent Hemorrhages due to a Chronic Expanding Encapsulated Intracranial Hematoma
title_sort case of recurrent hemorrhages due to a chronic expanding encapsulated intracranial hematoma
publisher Karger Publishers
series Case Reports in Neurology
issn 1662-680X
publishDate 2015-09-01
description Few case reports of encapsulated intracranial hematoma (EIH) exist, and the mechanisms underlying the onset and enlargement of EIH remain unclear. Here, we report on a 39-year-old woman with an EIH that repeatedly hemorrhaged and swelled and was ultimately surgically removed. In June 2012, the patient visited her local doctor, complaining of headaches. A magnetic resonance imaging (MRI) scan identified a small hemorrhage of approximately 7 mm in her right basal ganglia, and a wait-and-see approach was adopted. Six months later, her headaches recurred. She was admitted to our department after MRI showed tumor lesions accompanying the intermittent hemorrhaging in the right basal ganglia. After admission, hemorrhaging was again observed, with symptoms progressing to left-sided hemiplegia and fluctuating consciousness; thus, a craniotomy was performed. No obvious abnormal blood vessels were observed on the preoperative cerebral angiography. We accessed the lesion using a transcortical approach via a right frontotemporal craniotomy and removed the subacute hematoma by extracting the encapsulated tumor as a single mass. Subsequent pathological examinations showed that the hematoma exhibited abnormal internal vascularization and was covered with a capsule formed from growing capillaries and accumulating collagen fibers, suggesting that it was an EIH. No lingering neurological symptoms were noted upon postoperative follow-up. This type of hematoma expands slowly and is asymptomatic, with reported cases consisting of patients that already have neurological deficits due to progressive hematoma growth. Our report is one of a few to provide a clinical picture of the initial stages that occur prior to hematoma encapsulation.
topic Encapsulated intracranial hematoma
Fibrous capsule
Angiographically occult intracranial vascular malformation
Chronic encapsulated hematoma
url http://www.karger.com/Article/FullText/440610
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