Esquenazi Yoshua, Kerr Keith, Bhattacharjee Meenakshi B, Tandon Nitin
Vivian L Smith Department of Neurosurgery, University of Texas Medical School at Houston, Houston TX, USA.
Surg Neurol Int. 2013 Jun 12;4:80. doi: 10.4103/2152-7806.113357. Print 2013.
Dermoid tumors are benign congenital cystic lesions that usually present with local mass effect. Very rarely, they present as spontaneous ruptures. Traumatic rupture of these dermoid cysts is an extremely rare event and only a handful of such cases have been ever reported.
A 47-year-old female presented to our hospital with a ruptured intracranial dermoid cyst following a mild head injury. The ruptured cyst contents were disseminated into the subarachnoid and intraventricular compartments, resulting in an obstructive hydrocephalus. After medical stabilization, she underwent gross total resection of the cyst using combined transsylvian, transcortical-transventricular, and sub-frontal approaches. A ventriculo-peritoneal shunt was eventually also needed.
Traumatic rupture of an intracranial dermoid cyst is an extremely rare event and this is only the fourth such case reported in the literature. We presume that this rupture occurs due to sudden shifts in the cyst sac, which is adherent to some partially mobile intracranial contents. Although computed tomography (CT) is often adequate in making a diagnosis of this entity, magnetic resonance imaging (MRI) provides complete characterization of the extent of lipid dissemination, and is essential for operative planning. Intravenous steroids at presentation are helpful in managing the aseptic meningitis associated with rupture. Complete surgical resection is the goal, but must be weighed against the risk for injury to nearby vital structures. Hydrocephalus should be managed promptly, and patients should be monitored for it closely in the perioperative period. Even though the recurrence rate with subtotal resection is extremely rare, follow up should be done routinely.
皮样囊肿是良性先天性囊性病变,通常表现为局部占位效应。极少见的情况下,它们会表现为自发破裂。这些皮样囊肿的外伤性破裂是极其罕见的事件,仅有少数此类病例被报道过。
一名47岁女性因轻度头部受伤后出现颅内皮样囊肿破裂而就诊于我院。破裂囊肿的内容物播散至蛛网膜下腔和脑室内,导致梗阻性脑积水。在病情稳定后,她采用经外侧裂、经皮质 - 脑室和额下联合入路接受了囊肿全切术。最终还需要进行脑室 - 腹腔分流术。
颅内皮样囊肿的外伤性破裂是极其罕见的事件,这是文献中报道的第四例此类病例。我们推测这种破裂是由于囊肿囊壁突然移位所致,该囊肿与一些部分可移动的颅内内容物粘连。尽管计算机断层扫描(CT)通常足以诊断该疾病,但磁共振成像(MRI)可全面描述脂质播散的范围,对手术规划至关重要。就诊时静脉使用类固醇有助于处理与破裂相关的无菌性脑膜炎。手术全切是目标,但必须权衡对附近重要结构造成损伤的风险。应及时处理脑积水,并且在围手术期应对患者进行密切监测。即使次全切除后的复发率极低,也应常规进行随访。