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A patient with neurofibromatosis type 1 presenting with bilateralfrontal lobe infarctions following anterior communicating artery aneurysmrupture

机译:1型神经纤维瘤病患者伴双侧前交通动脉瘤后额叶梗死破裂

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摘要

Neurofibromatosis is a neurocutaneous genetic condition with dysplasia of the mesodermal and ectodermal tissues. Vascular abnormalities are well recognized in neurofibromatosis and cerebral aneurysms are rarely reported in literature. Here, we present a 20-year-old Sri Lankan female presented with headache, altered personality, disinhibited behaviour, and urinary incontinence. On imaging, she was found to have infarctions of both frontal lobes and evidence of a ruptured anterior communicating artery aneurysm with a small subarachnoid haemorrhage. Another small middle cerebral artery aneurysm was also seen in the angiogram. She was managed conservatively and gradually recovered. Because aneurysms in neurofibromatosis are usually asymptomatic and as rupture of such an aneurysm is rare, regular vascular screening is not recommended to all patients with neurofibromatosis. This is the first case report in literature in which a patient with neurofibromatosis presented with infarctions of both frontal lobes due to rupture of an anterior communicating artery aneurysm.
机译:神经纤维瘤病是具有中胚层和外胚层组织发育异常的神经皮肤遗传病。血管异常在神经纤维瘤病中广为人知,并且在文献中很少报道脑动脉瘤。在这里,我们介绍了一名20岁的斯里兰卡女性,她出现头痛,性格改变,行为减退和尿失禁。影像学检查发现她既有额叶梗塞,又有前交通动脉瘤破裂和少量蛛网膜下腔出血的证据。在血管造影中还发现了另一个小的大脑中动脉瘤。她被保守地对待并逐渐康复。由于神经纤维瘤病中的动脉瘤通常是无症状的,而且这种动脉瘤破裂的情况很少,因此不建议对所有神经纤维瘤病患者定期进行血管筛查。这是文献中第一个病例报告,其中神经纤维瘤病患者由于前交通动脉瘤破裂而出现两个额叶梗塞。

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