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基底节区缓慢进展性扩大血肿:3例报告及文献复习

[Slowly progressive expanding hematoma in the Basal Ganglia: a report of 3 cases and a literature review].

作者信息

Fujii Mutsumi, Takada Yoshiaki, Ohno Kikuo, Hokari Mitsuhiko, Arai Toshinari

机构信息

Department of Neurosurgery, Tokyo Medical and Dental University, Tokyo, Japan.

出版信息

Brain Nerve. 2012 Mar;64(3):295-302.

Abstract

We demonstrate and discuss slowly progressive expanding hematoma (SPEH) in the basal ganglia, which expands over 2 weeks. To our knowledge, there have been only 5 cases of sudden-onset SPEH of the basal ganglia. To this, we add 3 cases admitted our hospitals because of putaminal hemorrhage within 1.5 hours of onset. All hematomas exhibited "2 components of hematoma sign" on initial CT scans, which we termed the "TCH sign" characterized as an anterolateral fluid portion and a posteromedial solid portion. Follow-up CT scans revealed gradual expansion of the fluid component of the hematoma without rebleeding for the subacute phase. Two cases were treated surgically. The first case, a 47-year-old man, underwent ultrasonically guided hematoma aspiration on day 17 and the second case, a 37-year-old man, underwent hematoma removal by craniotomy on day 23 after onset. Their postoperative courses were uneventful. The third case, a 57-year-old man, improved without surgical treatment and the hematoma dissolved completely within 2 months. To an extent, the TCH sign on a CT scan can be related to SPEH. We reviewed previous reports, including those an chronic expanding intracerebral hematomas and chronic encapsulated intracerebral hematomas, and concluded that it requires approximately 1 month for encapsulation of the hematoma to emerge. We suggest a possible progressive mechanism of SPEH. At first, the hematoma is divided into a fluid and a solid portion. Local generation of osmotically active molecules by clot degradation may allow intravascular fluid to escape into the fluid portion of the hematoma. Edema fluid with leakage via the disrupted blood-brain barrier may also aggravate the fluid portion of the hematoma. The continuing inflammatory response leads to the emergence of a hematoma capsule similar to the membrane observed in cases of chronic subdural hematoma, followed by the secondary causes of hematoma expansion. We discuss feasible timing and surgical treatment methods.

摘要

我们展示并讨论了基底节区缓慢进展性扩大血肿(SPEH),其在2周内逐渐扩大。据我们所知,基底节区突发SPEH仅有5例。在此基础上,我们补充了3例因发病1.5小时内出现壳核出血而入住我院的病例。所有血肿在初次CT扫描时均表现出“血肿征的两个成分”,我们将其称为“TCH征”,其特征为前外侧液性部分和后内侧实性部分。随访CT扫描显示血肿的液性成分逐渐扩大,亚急性期无再出血。2例接受了手术治疗。第一例为47岁男性,在第17天接受了超声引导下血肿抽吸术;第二例为37岁男性,在发病后第23天接受了开颅血肿清除术。他们的术后病程顺利。第三例为57岁男性,未经手术治疗病情好转,血肿在2个月内完全溶解。在一定程度上,CT扫描上的TCH征可能与SPEH有关。我们回顾了既往报告,包括慢性扩大性脑内血肿和慢性包裹性脑内血肿的报告,并得出结论,血肿包膜的出现大约需要1个月时间。我们提出了一种可能的SPEH进展机制。起初,血肿分为液性和实性部分。血凝块降解产生的具有渗透活性的分子可能使血管内液体渗入血肿的液性部分。通过受损血脑屏障漏出的水肿液也可能加重血肿的液性部分。持续的炎症反应导致出现类似于慢性硬膜下血肿病例中观察到的血肿包膜,随后是血肿扩大的继发原因。我们讨论了可行的时机和手术治疗方法。

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