与脑裂畸形相关的血管异常、脂肪瘤和多微脑回畸形:发育和诊断见解。说明性案例。

Kevin K Kumar, Angus Toland, Nancy Fischbein, Martha Morrell, Jeremy J Heit, Donald E Born, Gary K Steinberg
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引用次数: 0

摘要

背景:脑裂是一种罕见的中枢神经系统畸形。颅内脂肪瘤也很罕见,约占大脑“肿瘤”的0.1%。据信,它们源于持续性原发性脑膜,这是一种神经嵴衍生的间充质,发展为硬脑膜和软脑膜。观察结果:作者报告了一例22岁男性脑裂引起的异位脂肪组织和非狩猎性动脉血管畸形。影像学显示右额灰质异常,并伴有疑似动静脉畸形,有出血迹象。脑磁共振成像显示,右额多发性微脑回衬于开口唇裂,脑室周围异位灰质,裂内脂肪,梯度回波低强度,与既往出血有关。组织学评估显示,成熟的脂肪组织具有大口径、厚壁、不规则的动脉。观察到壁画钙化和内皮下垫,提示无层流血流。没有动脉化的静脉或从动脉到静脉的直接过渡。含铁血黄素沉积不足,未出现出血。最终诊断符合异位成熟脂肪组织和脑膜脑瘢痕动脉。经验教训:这个原发性半月板衍生物与皮质发育不良相关的复杂发育不良的例子突出了诊断检查过程中从放射学和组织学角度的独特挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Vascular anomaly, lipoma, and polymicrogyria associated with schizencephaly: developmental and diagnostic insights. Illustrative case.

Vascular anomaly, lipoma, and polymicrogyria associated with schizencephaly: developmental and diagnostic insights. Illustrative case.

Vascular anomaly, lipoma, and polymicrogyria associated with schizencephaly: developmental and diagnostic insights. Illustrative case.

Vascular anomaly, lipoma, and polymicrogyria associated with schizencephaly: developmental and diagnostic insights. Illustrative case.

Background: Schizencephaly is an uncommon central nervous system malformation. Intracranial lipomas are also rare, accounting for approximately 0.1% of brain "tumors." They are believed to be derived from a persistent meninx primitiva, a neural crest-derived mesenchyme that develops into the dura and leptomeninges.

Observations: The authors present a case of heterotopic adipose tissue and a nonshunting arterial vascular malformation arising within a schizencephalic cleft in a 22-year-old male. Imaging showed right frontal gray matter abnormality and an associated suspected arteriovenous malformation with evidence of hemorrhage. Brain magnetic resonance imaging revealed right frontal polymicrogyria lining an open-lip schizencephaly, periventricular heterotopic gray matter, fat within the schizencephalic cleft, and gradient echo hypointensity concerning for prior hemorrhage. Histological assessment demonstrated mature adipose tissue with large-bore, thick-walled, irregular arteries. Mural calcifications and subendothelial cushions suggesting nonlaminar blood flow were observed. There were no arterialized veins or direct transitions from the arteries to veins. Hemosiderin deposition was scant, and hemorrhage was not present. The final diagnosis was consistent with ectopic mature adipose tissue and arteries with meningocerebral cicatrix.

Lessons: This example of a complex maldevelopment of derivatives of the meninx primitiva in association with cortical maldevelopment highlights the unique challenges from both a radiological and histological perspective during diagnostic workup.

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