Department of Neurosurgery, PGIMER, Chandigarh 160012, India.
Acta Neurochir (Wien). 2011 Jan;153(1):164-9; discussion 170. doi: 10.1007/s00701-010-0695-5. Epub 2010 May 27.
Parafalcine subdural empyema and those along the superior and inferior surface of the tentorium are rare entities. We present a series of 10 patients where we have attempted to describe the pathophysiology, clinical features, and management of subdural empyema.
The study group included 10 cases of falcotentorial subdural empyemas managed between 2004 and 2010. The mean age group was 14.4 years. Seven patients had empyema along the falx or superior surface of tent, and the remaining three had empyema along the inferior surface of tent. Fever, raised intracranial pressure symptoms, falx syndrome, and seizures were the usual presenting features. These patients had an indolent presentation as compared to convexity subdural empyemas. The diagnosis was made based on radiology. Chronic suppurative otitis media was a causative factor in five patients; in the remaining patients, the source was ascribed to be hematogenous. All patients were treated with antibiotic therapy (6 weeks) ± surgery. Two patients were treated conservatively, and the remaining eight patients underwent definitive surgery in the form of craniotomy (supratentorial)/craniectomy (infratentorial) and evacuation of pus. The pus was limited within two leaves, one adherent to the falx/tent and the other one to the pia-arachnoid of adjacent parenchyma. The wall along the falx or tent could be peeled off easily and was excised in all cases to lay open the cavity widely. The wall along pia-arachnoid was left as it is. Pus culture was positive in four and blood culture positive in two cases. There was only a single mortality in our series. The outcome was assessed by the Glasgow Outcome Scale. The mean duration of follow-up was for 18.8 months, and all patients who survived had a good outcome.
Falcotentorial empyema remains a rare entity. The presentation is indolent as compared to convexity subdural empyemas, possibly due to its limitation secondary to arachnoid adhesions at the junction of falx, tent, and convexity dura. The main stay of management remains craniotomy, evacuation, and partial excision of the wall, laying it completely open, unless it is extremely thin. With appropriate surgery and antibiotic therapy, a good outcome can be expected.
岩上窦和小脑幕上下的硬膜下积脓是罕见的疾病。我们介绍了一组 10 例患者,旨在描述硬膜下积脓的病理生理学、临床特征和治疗方法。
研究组包括 2004 年至 2010 年期间治疗的 10 例岩上窦-小脑幕硬膜下积脓患者。平均年龄组为 14.4 岁。7 例患者的积脓位于镰状窦或小脑幕上表面,其余 3 例患者的积脓位于小脑幕下表面。发热、颅内压升高症状、镰状窦征和癫痫发作是常见的表现。与凸面硬膜下积脓相比,这些患者的表现较为隐匿。根据影像学诊断。慢性化脓性中耳炎是 5 例患者的病因,其余患者的病因归因于血源性。所有患者均接受抗生素治疗(6 周)±手术治疗。2 例患者接受保守治疗,其余 8 例患者接受开颅术(幕上)/颅切除术(幕下)和脓液清除术。脓液局限于两层,一层附着于镰状窦/小脑幕,另一层附着于相邻脑实质的软脑膜。沿着镰状窦或小脑幕的壁很容易被剥离,并在所有病例中被切除,以广泛开放腔。沿着软脑膜的壁保留下来。4 例脓液培养阳性,2 例血培养阳性。本组仅有 1 例死亡。采用格拉斯哥预后量表评估预后。平均随访时间为 18.8 个月,所有存活患者的预后良好。
岩上窦-小脑幕硬膜下积脓仍然是一种罕见的疾病。与凸面硬膜下积脓相比,其表现较为隐匿,可能是由于蛛网膜在镰状窦、小脑幕和凸面硬脑膜交界处粘连,导致其局限。主要的治疗方法仍然是开颅术、引流和部分切除壁,使其完全开放,除非壁非常薄。通过适当的手术和抗生素治疗,可以获得良好的结果。