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Ruptured dermoid cyst of the lateral cavernous sinus wall with temporary symptoms: a case report
Journal of Medical Case Reports volume 10, Article number: 224 (2016)
Dermoid cysts are non-neoplastic tumors that arise from defects in the separation of the neuroectoderm. Cyst rupture rarely occurs spontaneously and the most common symptom is headache, followed by seizure. Although many cases of ruptured dermoid cysts present with symptoms, reports of cases that are asymptomatic, or where symptoms disappear, are rare.
We report the case of a 66-year-old Asian man with a history of sudden onset headache who was found to have high amounts of fat material in the subarachnoid space and a fat suppression mass in the left cavernous sinus. He underwent oral steroid therapy. Five days after starting medication his headache symptoms disappeared. Routine neurological imaging was then performed without surgical procedure. Magnetic resonance imaging revealed evidence of the remains of a static lesion 6 months after his first visit. He has remained headache free for 10 months since the initial event.
Although cases of ruptured dermoid cysts presenting with consistent symptoms have been commonly reported, until now there were few reports on asymptomatic cases or cases where symptoms disappeared. We believe that surgical intervention is unnecessary for ruptured dermoid cysts with minimal symptoms.
Dermoid cysts are rare tumors, accounting for 0.04–0.6 % of all intracranial tumors that arise from ectodermally committed cells at the time of closure of the neural groove between the third and fifth week of embryonic life [1, 2]. They frequently occur at suprasellar, frontobasal, temporobasal regions, and in the posterior fossa . They are benign, slow-growing tumors which rarely rupture. Dermoid cysts produce various symptoms, especially headache, seizure, cerebral ischemia, and meningitis [3, 4]. Although rupture of dermoid cysts typically occurs spontaneously, there are a few cases of traumatic rupture of dermoid cysts [5, 6]. Surgery is recommended in patients with symptomatic ruptured dermoid cysts. On the other hand, asymptomatic patients with ruptured dermoid cyst lesions are recommended for close observation, but to the best of our knowledge only eight cases with such observation have been described [3, 7–13]. We discuss the clinical features of ruptured dermoid cysts and analyze cases without surgery.
A 66-year-old Asian man presented with sudden onset headache. His past medical history was significant for intraductal papillary mucinous neoplasm. On physical examination, he was awake, alert, and his cranial nerves were intact. No neck stiffness was present. Laboratory tests were all within normal limits. A computed tomography (CT) scan of his head showed a hypodense lesion in the left cavernous sinus and many scattered fat density masses in the bilateral subarachnoid space (Fig. 1). A magnetic resonance imaging (MRI) scan of his brain revealed a 20 mm fat suppression mass and scattered small hyperintense lesions on T1-weighted image. The lesions were not enhanced with gadolinium infusion (Fig. 2). Radiographic diagnosis was ruptured cavernous sinus dermoid cyst. Oral steroid therapy with 30 mg prednisolone resulted in headache resolution 5 days later, so we decided to observe the patient with neurological imaging. The steroid was administrated for 28 days. He remained free of headache and convulsions. He did not develop double vision over the course of the follow-up. An MRI scan performed 6 months later revealed the parasellar mass and many fat droplets in the subarachnoid space unchanged since the initial MRI. At 10 months after the initial event, there was complete cessation of the headache and no seizures.
Dermoid cystic tumors arise from defects in the separation of the neuroectoderm at the time of neural tube closure during the third to fifth week of embryonic development [1, 2]. The cysts contain thick yellowish material consisting of sebaceous gland secretions and desquamated epithelium, in which a variable number of hairs is entangled . Rupture of intracranial dermoid cysts is rare. Cyst rupture usually occurs spontaneously. A few cases of rupture after head trauma have been reported [5, 6]. Although the exact mechanism of cyst rupture remains unknown, Stendel et al. hypothesized that glandular secretions, possibly increased by age-dependent hormonal changes, may lead to rapid enlargement and rupture . The most common symptom was headache, occurring in 31.8–32.6 % of the cases, followed by seizure in 26.5–29.5 %, and cerebral ischemia with sensory and/or motor hemisyndrome in 15.9–16.3 % [2, 4]. Ruptured dermoid cyst with chemical meningitis has been reported in 7–8.2 % of the cases, with psychosyndrome and visual disturbance present in 4.5 % [2, 4, 14].
The location of dermoid cysts were reported to be frontal base, frontal lobe, suprasellar, parasellar, Sylvian fissure, middle base, temporal lobe, hypothalamus, pineal, posterior fossa, fourth ventricle, cerebellopontine angle, and clivus . They are most often found in a sellar or parasellar location as well as the frontonasal region and frequently reside near the skull base . In our case, the dermoid cyst was located in the lateral wall of the left cavernous sinus. Dermoid cysts in the cavernous sinus are rare and only ten cases have been reported [1, 17–25]. The past cases of dermoid cysts in cavernous sinus presented various symptoms, such as diplopia in six cases, headache in five cases, blurring of vision in three cases, and seizure in one case. On neurological examination, third, fourth, fifth, and sixth nerve palsy were documented. In cases which were referred to therapeutic strategy, all patients underwent surgical resection. Diplopia was usually improved in cases with gross total removal. On the other hand, Akdemir et al. reported a case with no remarkable change in ophthalmoplegia . We have an interest in dermoid cysts of the cavernous sinus and observe that there is not always a resolution of symptoms after surgery, and that patients may become asymptomatic after oral steroid therapy due to the anti-inflammatory effect.
In the case reported by Liu et al., surgical resection is recommended in patients with symptomatic ruptured intracranial dermoid cyst . Although most cases resolve after surgery, there was relapse of symptoms and incidents of re-rupture in patients who underwent partial resection [15, 22, 26]. In cases without surgical resection, Liu et al. reported that close observation would be an acceptable option in these patients, although treatment of patients with asymptomatic lesions is not yet well codified . The number of reports that evaluate observation with regular neurological imaging is small and the natural history of ruptured dermoid cysts is uncertain. To the best of our knowledge only nine patients including our case have been reported to be treated conservatively. We reviewed patients who were subjected to conservative management (Table 1) [7–13]. Ruptured cysts were located in parasellar and suprasellar regions except for one case at the pineal region. Asymptomatic lesions accounted for only two cases, with other cases all having had initial symptoms. Neuroradiological findings were characterized by a lack of change in fat droplets of the subarachnoid space over the course of conservative management. Many reported cases which were treated by surgery presented with visual disturbance. On the other hand, there is no example of a report with visual disturbance in conservatively managed cases. In closely observed cases, the initial symptoms of ruptured dermoid cyst, including headache, seizure, meningitis and paresis, were present (with two asymptomatic exceptions), but most cases were uneventful and asymptomatic over the course of observation, with the exception of one with seizure. Headache is believed to be caused by the mass effect of the cyst as well as due to meningeal irritation caused by the rupture of the dermoid cyst . In our case, the dermoid cysts were too small to produce mass effects, so the oral steroid therapy which made the headaches disappear presumably decreased the meningeal irritation. A separate case in which steroid treatment was equally effective has been reported by Wang et al. . Therefore, we consider conservative treatment to be an approach which should be examined as a therapeutic alternative in cases with headache or controllable seizure without visual disturbance. But, the course of observation for ruptured intracranial dermoid cysts is so far largely anecdotal and unclear in the absence of a large series of long-term follow-up cases. We conclude that it is important for long-term follow-up cases of ruptured dermoid cyst to be systematically accumulated.
Ruptured dermoid cysts presenting with asymptomatic or disappearing symptoms are rare. The number of reports that evaluate observation with regular neurological imaging is small and the natural history of ruptured dermoid cysts is uncertain. We believe conservative treatment without surgery should be considered a therapeutic alternative in asymptomatic cases of ruptured dermoid cyst, or where symptoms disappear.
Lunardi P, Missouri P. Supratentorial dermoid cysts. J Neurosurg. 1991;75:262–6.
Stendel R, Pietilä TA, Lehmann K, Kurth R, Suess O, Brock M. Ruptured intracranial dermoid cysts. Surg Neurol. 2002;57:391–8.
Liu JK, Gottfried ON, Salzman KL, Schmidt RH, Couldwell WT. Ruptured intracranial dermoid cysts: clinical, radiographic, and surgical features. Neurosurgery. 2008;62:377–84.
El-Bahy K, Kotb A, Galal A, El-Hakim A. Ruptured intracranial dermoid cysts. Acta Neurochir (Wien). 2006;148:457–62.
Esquenazi Y, Kerr K, Bhattacharjee MB, Tandon N. Traumatic rupture of an intracranial dermoid cyst: Case report and literature review. Surg Neurol Int. 2013;4:80.
Park SK, Cho KG. Recurrent intracranial dermoid cyst after subtotal removal of traumatic rupture. Clin Neurol Neurosurg. 2012;114:421–4.
Corr P, de Villiers P. Ruptured intracranial dermoid cyst. S Afr Med J. 2000;90(7):697.
Indulkar S, Hsich GE. Spontaneous rupture of intracranial dermoid cyst in a child. Neurology. 2011;77:2070.
Kucera JN, Roy P, Murtagh R. Ruptured intracranial dermoid cyst manifesting as new onset seizure: a case report. J Radiol Case Rep. 2011;5(4):10–8. doi:10.3941/jrcr.v5i4.592. Epub 2011 Apr 1.
Messori A, Polonara G, Serio A, Gambelli E, Salvolini U. Expanding experience with spontaneous dermoid rupture in the MRI era: diagnosis and follow-up. Eur J Radiol. 2002;43:19–27.
Rajapakse A, Diack A. Ruptured intracranial dermoid: an unusual cause of headache in an older patient. Headache. 2008;48:294–6.
Wang YM, Chang TP, Lo CP, Tu MC. Spontaneous rupture of intracranial dermoid cyst with chemical meningitis. J Emerg Med. 2013;44:e275–6.
Wilms G, Casselman J, Demaerel P, Plets C, De Haene I, Baert AL. CT and MRI of ruptured intracranial dermoids. Neuroradiology. 1991;33:149–51.
Das CJ, Tahir M, Debnath J, Pangtey GS. Neurological picture. Ruptured intracranial dermoid. J Neurol Neurosurg Psychiatry. 2007;78:624–5.
Kikuchi Z, Takemura S, Kuge A, Sato S, Kayama T. Case report: spontaneous rupture of an asymptomatic intracranial dermoid. No Shinkei Geka. 2010;38(5):455–62.
Arseni C, Dănăilă L, Constantinescu AI, Carp N, Decu P. Cerebral dermoid tumours. Neurochirurgia (Stuttg). 1976;19(3):104–14.
Abdelouafi A, Ousehal A, Gharbi A, Ait Benali S, El Kamar A, Kadiri R. Cavernous sinus dermoid cyst with unusual parapharyngeal development. J Neuroradiol. 2000;27(2):140–3.
Akdemir G, Daglioglu E, Ergungor MF. Dermoid lesion of the cavernous sinus: Case report and review of the literature. Neurosurg Ver. 2004;27:294–8.
Chen YF, Liu HM, Tu YK. Dermoid cyst as a dumbbell-shaped tumour of the cavernous sinus. Pediatr Radiol. 2003;33:72.
Dange N, Mahore A, Goel A. Ruptured giant dermoid cyst of the cavernous sinus. J Clin Neurosci. 2010;17:1056–8.
DeMonte F, Al-Mefty O. Ruptured dermoid tumor of the cavernous sinus associated with the syndrome of fat embolism: Case report. J Neurosurg. 1992;77:312–5.
North KN, Anthony JH, Johnston IH. Dermoid of cavernous sinus resulting in isolated oculomotor nerve palsy. Pediatr Neurol. 1993;9:221–3.
Nakagawa K, Ohno K, Nojiri T, Hirakawa K. Interdural dermoid cyst of the cavernous sinus presenting with oculomotor palsy: case report. No Shinkei Geka. 1997;25(9):847–51.
Rato RM, Pappamikail LB, Ratilal BO, Luiz CA. Dermoid tumor of the lateral wall of the cavernous sinus. Surg Neurol Int. 2012;3:10.
Tun K, Celikmez RC, Okutan O, Gurcan O, Beskonakli E. Dermoid tumour of the lateral wall of the cavernous sinus. J Clin Neurosci. 2008;15:820–3.
Jamjoom AB, Cummins BH. The diagnosis of ruptured intracranial dermoid cysts. Br J Neurosurg. 1989;3:609–12.
YK drafted and edited the manuscript. HO, TS, MU, HT, HI, KO and YT contributed to the writing of the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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Kosuge, Y., Onodera, H., Sase, T. et al. Ruptured dermoid cyst of the lateral cavernous sinus wall with temporary symptoms: a case report. J Med Case Reports 10, 224 (2016). https://doi.org/10.1186/s13256-016-1007-3
- Cavernous sinus
- Dermoid cyst