Janssen Insa K, Haemmerli Julien, Bartoli Andrea, Joory Melvin, Richards Emily, Schaller Karl, Nouri Aria
Department of Neurosurgery, Hôpitaux Universitaires de Genève, Geneva, Switzerland.
Department of Radiodiagnostics and Interventional Radiology, CHUV, Lausanne, Switzerland.
Neurotrauma Rep. 2024 Aug 22;5(1):787-799. doi: 10.1089/neur.2024.0065. eCollection 2024.
The presence of a calcified or ossified chronic cranial epidural hematoma (EDH) is rare and has been described in only a few case reports in the literature. Consequently, clear treatment strategies remain elusive and may entail conservative and surgical approaches. In this study, we performed a systematic review of reported cases to evaluate the clinical course and treatment options for these patients. A comprehensive systematic search of two databases was performed, and information on patient characteristics, symptomatology, and treatment was extracted from eligible articles. A total of 56 cases were included in our analyses. Forty patients were male, 16 were female, with an average age of 21.38 years at the time of diagnosis. Assumed etiology was previous trauma in 35 cases, previous cranial surgery in 17 patients, and birth trauma and epidural bleeding after the utilization of the Mayfield clamp in 1 case each. The origin remained unclear in two cases. The time between trauma or surgery and diagnostics ranged between one and a half weeks and 50 years, with a median of 4 years (SD 9.8 years). The symptoms were very heterogeneous, ranging from acute neurological deterioration to chronic symptoms. In 15 cases, patients were asymptomatic, and cranial imaging was performed as part of a new trauma or a screening for other disease. Forty-one patients received surgical treatment by craniotomy and hematoma evacuation, and 13 patients were treated conservatively. In two cases, the liquid hematoma portion was aspirated through a burr hole. The localization of calcified or ossified EDH was mainly supratentorial. Young male patients most commonly present with calcified or ossified EDH after trauma, according to the epidemiological trend of acute EDH. Clinical presentation varies from asymptomatic to severe neurological deficits and signs of increased intracranial pressure. There is no standardized treatment; decisions must be made on an individual basis.
钙化或骨化的慢性硬膜外血肿(EDH)较为罕见,文献中仅有少数病例报告对此进行过描述。因此,明确的治疗策略仍不明确,可能需要采取保守和手术治疗方法。在本研究中,我们对已报道的病例进行了系统回顾,以评估这些患者的临床病程和治疗选择。我们对两个数据库进行了全面的系统检索,并从符合条件的文章中提取了患者特征、症状和治疗方面的信息。我们的分析共纳入了56例病例。其中40例为男性,16例为女性,诊断时的平均年龄为21.38岁。推测病因方面,35例为既往创伤,17例为既往颅脑手术,各有1例分别为出生创伤和使用梅菲尔德头架后的硬膜外出血。2例病因不明。创伤或手术与诊断之间的时间间隔为1.5周至50年,中位数为4年(标准差9.8年)。症状非常多样,从急性神经功能恶化到慢性症状不等。15例患者无症状,颅脑成像作为新创伤的一部分或其他疾病筛查的一部分进行。41例患者接受了开颅血肿清除手术治疗,13例患者接受了保守治疗。2例患者通过钻孔抽吸了血肿的液体部分。钙化或骨化的EDH主要位于幕上。根据急性EDH的流行病学趋势,年轻男性患者创伤后最常出现钙化或骨化的EDH。临床表现从无症状到严重神经功能缺损和颅内压升高迹象不等。目前尚无标准化治疗方法;必须根据个体情况做出决策。