Cisneros Oscar, Rehmani Razia, Garcia de de Jesus Katherine
Internal Medicine, St. Barnabas Hospital Health System / Albert Einstein College of Medicine, Bronx, USA.
Neuroradiology, St. Barnabas Hospital Health System, Bronx, USA.
Cureus. 2019 Apr 3;11(4):e4371. doi: 10.7759/cureus.4371.
Cavernous malformations are congenital or acquired vascular abnormalities. They are uncommon entities with an incidence of 0.5% of the general population and usually are unnoticed until a hemorrhagic event occurs. Cavernomas can be concurrently seen with developmental venous anomalies (DVAs) in 20% (range 20%-40%) of cases, in which case they are known as mixed vascular malformations. We report a case of a healthy young adult, who presented with acute onset of headache, dizziness, and nausea with intermittent episodes of vomiting for four days. Brain tomography imaging at presentation revealed likely multiple foci of intracranial hemorrhage; however, magnetic resonance imaging (MRI) showed findings suggestive of an underlying cavernoma that had bled, in addition to a coexisting DVA. The patient was discharged home with no deficits. Outpatient follow-up five months later revealed no symptoms or neurologic deficits.
海绵状血管畸形是先天性或后天性血管异常。它们是罕见的病变,在普通人群中的发病率为0.5%,通常在出血事件发生之前未被发现。在20%(范围为20%-40%)的病例中,海绵状血管瘤可与发育性静脉异常(DVA)同时出现,在这种情况下,它们被称为混合性血管畸形。我们报告一例健康年轻成年人病例,该患者出现急性头痛、头晕和恶心,并伴有间歇性呕吐四天。就诊时的脑部断层扫描成像显示可能存在多个颅内出血灶;然而,磁共振成像(MRI)显示除了并存的DVA外,还发现有潜在的已出血海绵状血管瘤的迹象。患者出院时无功能缺损。五个月后的门诊随访显示无任何症状或神经功能缺损。