|Year : 2018 | Volume
| Issue : 4 | Page : 1273-1275
Secondary arachnoid cyst – A late complication of craniotomy: A case report and review of literature
Mostafa Osman, Ahmed Diraz
Department Of Neurosurgery, Dr. Soliman Fakeeh Hospital, Jeddah, Saudi Arabia
|Date of Web Publication||23-Oct-2018|
Dr. Mostafa Osman
Dr. Soliman Fakeeh Hospital, Jeddah
Source of Support: None, Conflict of Interest: None
Arachnoid cyst can be defined as cerebral-spinal fluid entrapment within the central nervous system. It may occur primarily as a congenital malformation or secondary as a complication following trauma, infection, bleeding, or surgical manipulation. Congenital arachnoid cyst usually asymptomatic and cause no pressure symptoms. No treatment is needed unless size increase and cause pressure symptoms and increased intracranial pressure. We report a case presented to the hospital with neurological signs of increased intracranial pressure, 3 years Post aborted craniotomy for meningioma resection. Radiological imaging showed postoperative newly developed arachnoid cyst with mass effect. He underwent the urgent cerebral spinal fluid diversionary procedure with cystoperitoneal shunt.
Keywords: Arachnoid cyst, complication, congenital, craniotomy, secondary
|How to cite this article:|
Osman M, Diraz A. Secondary arachnoid cyst – A late complication of craniotomy: A case report and review of literature. Asian J Neurosurg 2018;13:1273-5
|How to cite this URL:|
Osman M, Diraz A. Secondary arachnoid cyst – A late complication of craniotomy: A case report and review of literature. Asian J Neurosurg [serial online] 2018 [cited 2019 Feb 16];13:1273-5. Available from: http://www.asianjns.org/text.asp?2018/13/4/1273/243737
| Introduction|| |
Arachnoid cysts are classified as developmental cysts; they were first described in 1831. These cysts lie between 2 membranes of normal arachnoid matter and are more properly described as intra-arachnoid cysts. Congenital or developmental arachnoid cysts differ from secondary or acquired arachnoid cysts, as the latter are loculations of cerebral spinal fluid (CSF) surrounded by arachnoid scarring.
Most commonly, they are found within the middle cranial fossa with an incidence of 42% followed by retrocerebellar and convexity locations. About 60%–90% of all patients with developmental arachnoid cysts are children with a male-to-female predominance of approximately 2:1.
| Case Report|| |
We report a case of 39-year-old gentleman presented to the emergency room (ER) with acute onset headache of 3 weeks' duration complicated with vomiting and fits. He had a surgical history of previous incomplete resection of right medial sphenoid wing meningioma, 3 years ago. Surgery report justified incomplete resection due to intraoperative severe hypotension.
Clinically, the patient was conscious. He had complete right 3rd nerve palsy with optic atrophy and no perception of light with associated corneal opacity developed after the previous surgery as quoted by patient and relatives. He can count fingers by the left eye, and there is severe papilledema on the left side.
Computed tomography (CT) brain and then magnetic resonance imaging (MRI) brain with contrast showed right-sided big temporal cyst with severe mass effect and impending uncal herniation associated with increasing size of the right medial sphenoid wing Space occupying lesion [Figure 1].
|Figure 1: Axial magnetic resonance imaging brain with contrast before the first surgery, showing extra-axial heterogonous mass (meningioma) is seen in the right para-sellar region|
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The patient was admitted from ER and received dexamethasone and loading dose of phenytoin and then maintenance dose. After patient stabilized, it was decided to treat the symptomatizing big right temporal cyst by cystoperitoneal shunt as a first stage [Figure 2]. The cyst seems to be progressively enlarging postoperative acquired arachnoid cyst as evidenced on F/U MRI brain study; preoperative [Figure 3] and postoperative. Pathological examination of cyst fluid ruled-out malignant or inflammatory cells [Figure 4].
|Figure 2: MRI Brain with contrast, 3 years after the first surgery, showing interval development of large cyst (black arrow), causing mass effectwith midline shift|
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|Figure 3: Coronal magnetic resonance imaging brain with contrast showing extra-axial heterogonous mass in the right parasellar region bounded medially by the internal carotid artery and cavernous sinus, Superiorly by the middle cerebral artery laterally by the temporal lobe and a newly formed cyst (arrow) in the previously dissected surgical corridor.|
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|Figure 4: Axial CT Brain showing Interval insertion of the right-sided ventriculoperitoneal shunt with mild interval improvement in the hydrocephalus and midline shift Stable amount of surrounding vasogenic edema with decrease in the size of cystic|
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Later on, the patient needs surgical intervention for debulking of the medial sphenoid meningioma with or without radiosurgery if needed.
| Discussion|| |
Arachnoid cysts are extra-axial, nonneoplastic CSF collection, localized to the arachnoid membrane within the central nervous system. Arachnoid cysts may be spinal, or intracranial (most common locations are the middle fossa), the suprasellar region (near the third ventricle) and the posterior fossa, where they may be associated with headache and seizures, with focal neurologic signs occurring less frequently.
Secondary type of arachnoid cyst occurs as a sequel of archnoidal tissue injury following direct irritation of the arachnoid matter by the inflammatory mediators; whether endogenous from the blood product or exogenous endotoxins from bacterial infections, come in contact with the leptomeninges. Adhesive arachnoiditis with CSF accumulation through a slit-valve mechanism with no exchange with CSF circulation leads to cyst formation. Sometimes, cyst size increases with time causing pressure symptoms and marked increase in the intracranial pressure.
They usually follow CSF density and intensity in CT and MRI, respectively. They do not enhance with contrast. Diffusion-weighted imaging fails to reveal restriction of water diffusion, which helps differentiate arachnoid cysts from epidermoid tumors.
Grossly, arachnoid cysts have thin translucent to thicker, more opaque membranes. The cyst contents are composed of clear fluid, with occasional xanthochromic discoloration if there has been prior hemorrhage.
However, it has been hypothesized that these cysts may also occur after events that produce an inflammatory process in the arachnoid membranes, such as surgical manipulation and the presence of blood in the subarachnoid space. This leptomeningeal inflammation may result in adhesive arachnoiditis with impairment of CSF dynamics, circulation, and CSF loculation.
Fujimura et al. reported a case of visual disturbance due to optochiasmal arachnoiditis and foreign body granuloma 9 months after surgery for aneurysm in which cotton wrapping was used. The authors recommended the avoidance of the use of the cotton sheet close to the optic nerve. This foreign material may induce a granulomatous reaction known as a “muslinoma” or “gauzoma” (Muslin-induced arachnoiditis). Many cases reported following bleeding issues, whether post coiled ruptured aneurysm or post evacuation of subdural bleeding raise the possibility of arachnoid matter irritation from direct contact with blood product.,
In patients with symptomatic arachnoid cysts, treatment may lead to relief of focal neurological deficits; treatment modalities involve endoscopic or open fenestration and shunt placement.
| Conclusion|| |
However, arachnoiditis seems to be unavoidable issue, meticulous deal with the arachnoid matter with trial of bloodless field would decrease the possibility of such a problem.
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Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2], [Figure 3], [Figure 4]