Đang cập nhật

Đang cập nhật

SUMMARY A basilar tip artery bifurcation aneurysm was diagnosed incidentally in a 69-year-old female patient. She was a normal her medical history. The MRI revealed a non-ruptured aneurysm with a maximum fundus diameter 4.9mm. Selective cerebral angiography confirmed the presence of a wide-necked aneurysm with a mean transverse diameter of 5mm and a mean height of 3mm; the neck width was 4.9mm. With this complex anatomy, the multidisciplinary team recommended endovascular treatment of the aneurysm with the WEB device. The procedure was performed with dual antiplatelet therapy (75 mg aspirin PO daily 3 days and 180 mg ticagrelor PO daily 2 days prior to the intervention). Immediately after placement of the WEB device, DSA showed complete occlusion of the aneurysm but has thromboembolic event in P3 posterior cerebral artery and no deficit. Postoperatively the patient received dual antiplatelet therapy for 5 days and continued 75 mg aspirin PO for 2 weeks, ticagrelor was discontinued. The patient was discharged 2 days after the intervention without any neurological symptoms. Follow-up by MRI at 3, 6, by MRI and DSA 12 months after treatment confirmed the stable obliteration of the aneurysm without recurrence or reperfusion. The value of the WEB device in the endovascular treatment of wide-necked basilar tip artery bifurcation aneurysms is the main topic of this chapter.

Bệnh nhân nữ 37 tuổi, đi kiểm tra sức khỏe. Tiền căn: không có tiền căn bệnh lý Các xét nghiệm SGOT, SGPT, bilirubin, CTM, chức năng thận trong giới hạn bình thường

Intracranial lipomas represent rare congenital malformations, accounting for less than 1% of intracranial tumours. Lipoma of corpus callosum, the commonest variety of all intracranial lipomas (40%-50%), is associated with varying degrees of dysgenesis of corpus callosum and generally remains asymptomatic.

Renal tumors in the Phakomatosis disease, what to note: two case report SUMMARY Phakomatosis are a group of neurocutaneous disorders characterised by involvement of structures that arise from the embryonic ectoderm , consist of central nervous system, skin ,eyes and others: kidney, heart, lung… In this article we focus on the incidence of renal tumors in Tuberous sclerosis, one of the common diseases in Phakomatosis. Tuberous sclerosis is a rare neurocutaneous disorder (phakomatosis) characterized by the development of multiple benign tumours in various organs, including the kidneys. Tuberous sclerosis complex has several renal manifestations including angiomyolipomas (AML) and renal epithelial neoplasms. Angiomyolipomas is found in 40% of patients with tuberous sclerosis, and its most common complication is ruptures due to aneurysms. We present two cases was diagnosed with bilateral angiomyolipomas in tuberculosis and emphasizes the importance of the diagnosis and choice of appropriate treatment for each patient. Key words : Phakomatosis, renal tumor