Vilela P, Saraiva P, Goulão A
Serviço de Neurorradiologia, Hospital Garcia de Orta, Av. Prof. Torrado Silva. Pragal, 2801-591, Almada, Portugal.
Neuroradiology. 2005 Feb;47(2):91-6. doi: 10.1007/s00234-004-1290-3. Epub 2005 Jan 21.
A 33-year-old female with a longstanding history of seizures was admitted to our hospital with subarachnoid haemorrhage (SAH). Computed tomography (CT), magnetic resonance imaging (MRI) and digital subtraction angiography (DSA) depicted a vascular fat-containing lesion overlying a right frontal cortical polymicrogyria. The diagnosis of angiolipoma was established. Conservatory management was undertaken with full recovery. She has been followed for 5 years since, with neither re-bleeding nor morphologic change of the lesion. This is a rare intracranial lesion, with only 11 intracranial angiolipomas published in the literature, and is the first case reported which is associated with SAH caused by this lesion.
一名有长期癫痫病史的33岁女性因蛛网膜下腔出血(SAH)入住我院。计算机断层扫描(CT)、磁共振成像(MRI)和数字减影血管造影(DSA)显示右额叶皮质多小脑回上方有一个含血管脂肪的病变。确诊为血管脂肪瘤。采取保守治疗,患者完全康复。此后对她进行了5年的随访,病变既未再次出血,形态也未改变。这是一种罕见的颅内病变,文献中仅报道过11例颅内血管脂肪瘤,该病例是首例报道的由该病变导致SAH的病例。