Sheikh Hassan Mohamed, Osman Sidow Nor, Adam Bakar Ali, Adani Abdulkamil Abdullahi
Department of Neurology, Mogadishu Somali Turkish Training and Research Hospital, Somalia.
Department of Internal Medicine, Mogadishu Somali Turkish Training and Research Hospital, Somalia.
Ann Med Surg (Lond). 2022 Apr 28;77:103674. doi: 10.1016/j.amsu.2022.103674. eCollection 2022 May.
and importance: Weber's syndrome is a rare type of brain stem stroke syndrome that is characterized by ipsilateral oculomotor nerve palsy and contralateral hemiparesis. The most common etiology is a midbrain infarction caused by occlusion of the paramedian branches of the posterior cerebral artery or the perforating branches of the basilar bifurcation. Although there are many multiple brainstem strokes, it is uncommon to see this syndrome.
Here we present a case of a 62-year-old male hypertensive patient who presented with a one-week history of cognitive dysfunction, left hemiparesis, right eye ptosis, and right medial gaze palsy (oculomotor nerve palsy). Diffusion MRI showed milimetric diffusion restriction in the right side of the mesencephalon, consistent with an acute infarct. Based on the clinical and radiological findings, a diagnosis of Weber's syndrome was made. The patient was treated with antiplatelet and Piracetam along with strict blood pressure control. There was a massive improvement in the patient's condition on the follow-up visit three weeks later.
Weber's syndrome is a rare brainstem stroke due to midbrain infarction and is characterized by crossing hemiplegia consisting of ipsilateral occulomotor nerve palsy and contralateral limb weakness due to damage to the corticospinal tract. Despite it being a brainstem stroke infarct, it carries a good prognosis if it is early treated along with strict control of the risk factors such as hypertension in this case. Our case had massive clinical improvement within three weeks of medical treatment and risk factor control.
This case highlights the classic rare syndrome of brainstem stroke presenting with crossing hemiparesis due to midbrain infarction. This syndrome has a favorable prognosis.
及其重要性:韦伯综合征是一种罕见的脑干卒中综合征,其特征为同侧动眼神经麻痹和对侧偏瘫。最常见的病因是大脑后动脉旁正中分支或基底动脉分叉处穿支闭塞导致的中脑梗死。虽然脑干有多处卒中,但出现这种综合征并不常见。
我们在此报告一例62岁男性高血压患者,有一周的认知功能障碍、左侧偏瘫、右眼上睑下垂和右内侧凝视麻痹(动眼神经麻痹)病史。磁共振扩散加权成像显示中脑右侧有毫米级的扩散受限,符合急性梗死表现。根据临床和影像学检查结果,诊断为韦伯综合征。患者接受了抗血小板药物和吡拉西坦治疗,并严格控制血压。三周后的随访中,患者病情有显著改善。
韦伯综合征是一种由中脑梗死引起的罕见脑干卒中,其特征为交叉性偏瘫,即同侧动眼神经麻痹和因皮质脊髓束受损导致的对侧肢体无力。尽管它是脑干梗死性卒中,但如果早期治疗并严格控制危险因素,如本例中的高血压,预后良好。我们的病例在药物治疗和危险因素控制三周内有显著的临床改善。
本病例突出了因中脑梗死导致交叉性偏瘫的典型罕见脑干卒中综合征。该综合征预后良好。