Akins Paul T, Axelrod Yekaterina K, Ji Cheng, Ciporen Jeremy N, Arshad Syed T, Hawk Mark W, Guppy Kern H
Department of Neurosurgery, Permanente Medical Group, Kaiser Sacramento Medical Center, Sacramento, CA 95825.
Surg Neurol Int. 2013 Jun 19;4:85. doi: 10.4103/2152-7806.113651. Print 2013.
Cerebral venous sinus thrombosis (CVST) can cause elevated intracranial pressure, hemorrhagic venous infarct, and cortical subarachnoid hemorrhage. We present a case series and literature review to illustrate that CVST can also present with subdural hematoma (SDH).
Chart review was completed on a retrospective case series of CVST with spontaneous SDH. We also conducted a literature search. Over a 6 year interval, three patients with CVST and SDH were admitted to the neurointensive care unit. A 38-year-old woman had both SDH and a hemorrhagic venous infarct associated with a transverse sinus thrombosis. She was managed conservatively with long-term anticoagulation. A 68-year-old woman presented with an acute SDH requiring craniotomy and a thrombosed cortical vein was noted intraoperatively. Computed tomography venography showed thrombosis of the superior sagittal sinus. She had polycythemia vera with the V617 Jak2 gene mutation and was managed with aspirin and hydroxyurea. A 60-year-old male had recurrence of a spontaneous convexity SDH requiring reoperation. Neuroimaging identified ipsilateral transverse sinus thrombosis with retrograde flow into the opposite sinus. Manometry demonstrated elevated venous pressures and these normalized after thrombectomy. Angiography performed after endovascular treatment demonstrated a normal venous drainage pattern. There have been limited reports of SDH complicating CVST in the literature.
This case series and literature review demonstrates that CVST can also present with spontaneous SDH with or without associated venous infarctions. Treatment must be individualized. This is the first published description of endovascular thrombectomy for recurrent symptomatic SDH due to CVST.
脑静脉窦血栓形成(CVST)可导致颅内压升高、出血性静脉梗死和皮质下蛛网膜下腔出血。我们呈现一个病例系列及文献综述,以说明CVST也可表现为硬膜下血肿(SDH)。
对一组伴有自发性SDH的CVST回顾性病例系列进行了病历审查。我们还进行了文献检索。在6年期间,3例患有CVST和SDH的患者入住神经重症监护病房。一名38岁女性同时患有SDH和与横窦血栓形成相关的出血性静脉梗死。她接受了长期抗凝的保守治疗。一名68岁女性表现为急性SDH,需要进行开颅手术,术中发现一条皮质静脉血栓形成。计算机断层扫描静脉造影显示上矢状窦血栓形成。她患有伴有V617 Jak2基因突变的真性红细胞增多症,接受阿司匹林和羟基脲治疗。一名60岁男性自发性凸面SDH复发,需要再次手术。神经影像学检查发现同侧横窦血栓形成,并伴有血液逆流至对侧窦。测压显示静脉压升高,血栓切除术后这些压力恢复正常。血管内治疗后进行的血管造影显示静脉引流模式正常。文献中关于SDH并发CVST的报道有限。
该病例系列和文献综述表明,CVST也可表现为伴有或不伴有相关静脉梗死的自发性SDH。治疗必须个体化。这是首次发表的关于因CVST导致复发性有症状SDH的血管内血栓切除术的描述。