Nguyen Christopher M, Stauber Jessica, Baliss Michelle, Reynoso David
Internal Medicine, University of Texas Medical Branch at Galveston, Galveston, USA.
Medicine, University of Texas Medical Branch at Galveston, Galveston, USA.
Cureus. 2020 Jun 21;12(6):e8732. doi: 10.7759/cureus.8732.
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant genetic condition associated with mucocutaneous and visceral arteriovenous malformations (AVMs), including pulmonary AVMs, which predispose patients to systemic paradoxical emboli that can lead to brain abscesses. Intraventricular rupture of brain abscess (IVROBA) is a feared complication with a high mortality rate. Here, we present a case with brain abscesses complicated by IVROBA and ventriculitis as the initial presentation of HHT in an undiagnosed patient. We also discuss the diagnostic and therapeutic approach that resulted in this patient's clinical improvement.
遗传性出血性毛细血管扩张症(HHT)是一种常染色体显性遗传病,与皮肤黏膜及内脏动静脉畸形(AVM)相关,包括肺动静脉畸形,这使患者易发生可导致脑脓肿的系统性反常栓塞。脑脓肿脑室破裂(IVROBA)是一种可怕的并发症,死亡率很高。在此,我们报告一例以脑脓肿合并IVROBA及脑室炎为首发表现的未确诊HHT患者。我们还讨论了使该患者临床症状改善的诊断和治疗方法。