Arachnoid Cyst in the Middle
Cranial Fossa with Post-Traumatic Symptoms
1. Cause and Etiology
Arachnoid cysts are
benign, fluid-filled sacs within the arachnoid membrane, one of the
three layers of the meninges surrounding the brain and spinal cord. They are
typically filled with cerebrospinal fluid (CSF) and may be:
- Congenital
(Primary): The majority are thought to arise
from developmental anomalies during embryogenesis, such as splitting or
duplication of the arachnoid membrane.
- Acquired
(Secondary): Less commonly, cysts may
form due to trauma, infection, hemorrhage, or post-surgical changes that
create a CSF-filled cavity within or between arachnoid layers.
In the case of
post-traumatic symptoms, trauma often does
not cause the cyst de novo but rather provokes symptoms from a preexisting cyst by:
- Rupture
or hemorrhage into the cyst
- Rapid
expansion due to CSF dynamics
- Increased
intracystic pressure
- Mass
effect on adjacent structures
2. Pathophysiology
- Arachnoid
cysts do not communicate freely
with the subarachnoid space, which can allow fluid accumulation.
- In
the middle cranial fossa,
the cyst can compress the temporal
lobe, mesial structures,
or optic pathway, depending
on size and exact location.
- Trauma
may alter CSF circulation or induce bleeding
within or around the cyst, enlarging it and increasing pressure on
adjacent brain tissue.
- Expansion
of the cyst may lead to:
- Elevated intracranial pressure
- Temporal lobe dysfunction
- Visual disturbances
or seizures
3. Epidemiology
- Incidence
in the general population: ~1–2% on brain MRI.
- Most
common in children and young adults;
male predominance.
- The
middle cranial fossa
(Sylvian fissure region) is the most frequent site (up to 50% of all
arachnoid cysts).
- Often
asymptomatic, but up to
20–30% may present with symptoms due to size or complications.
4. Clinical Presentation (Especially
Post-Traumatic)
In cases where a
previously asymptomatic cyst becomes symptomatic after minor head trauma, patients
may experience:
- Headache (persistent or worsened)
- Dizziness or vertigo
- Nausea, vomiting
- Seizures
- Focal neurological deficits
(e.g., visual field cuts if optic pathways are involved)
- Cognitive or behavioral changes
- Symptoms of increased intracranial pressure (ICP):
drowsiness, papilledema
5. Imaging Features
Modality of
choice: CT and MRI
- CT Scan:
- Well-defined, hypodense (CSF density) lesion
- No
enhancement or calcification
- Possible
mass effect (e.g.,
effacement of temporal horn, midline shift)
- Bony remodeling of the adjacent skull in
chronic cases
- MRI:
- T1: Hypointense (similar to
CSF)
- T2: Hyperintense
- FLAIR: No signal (unless
proteinaceous or hemorrhagic)
- DWI: No restricted diffusion
(helps distinguish from epidermoid cyst)
- No enhancement with gadolinium
Post-traumatic
complications may include:
- Hemorrhage within the cyst
(hyperintensity on T1)
- Subdural hygroma or hematoma
- Enlargement or cyst rupture
6. Treatment
Treatment depends on symptom severity, cyst size, and evidence of mass effect.
🔹
Observation (Asymptomatic or
minor symptoms)
- Regular
clinical and radiological follow-up (MRI)
- No
surgery unless progression
🔹
Surgical Intervention (Indicated
if symptomatic or progressive)
- Microsurgical fenestration
(open craniotomy)
- Creating
communication with the subarachnoid space
- Endoscopic fenestration
- Minimally
invasive, increasingly preferred
- Cystoperitoneal shunting
- Used
in select cases with hydrocephalus or failure of fenestration
7. Prognosis
- Generally
excellent prognosis with
proper management
- Most
patients recover well after surgical intervention
- Recurrence is rare
but possible, especially in shunted patients
- Without
intervention, large symptomatic cysts may lead to:
- Chronic
increased ICP
- Cognitive
delay (especially in children)
- Seizure
disorders
- Visual
impairment
Summary
|
Aspect |
Summary |
|
Etiology |
Mostly congenital;
trauma can provoke symptoms |
|
Pathophysiology |
CSF-filled cyst
compresses adjacent structures |
|
Epidemiology |
~1–2% population;
middle cranial fossa most common |
|
Symptoms |
Headache, dizziness,
seizures, increased ICP |
|
Imaging |
CSF-like signal, mass
effect, no enhancement |
|
Treatment |
Observation or
surgical fenestration/shunting |
|
Prognosis |
Excellent with
intervention; poor if untreated and large |
=====================================
Case Study: Post-Traumatic Headache and Dizziness in a 6-Year-Old Boy
Arachnoid Cyst
History and Imaging
-
A 6-year-old boy presented with persistent headache and dizziness lasting for two days following a minor head injury sustained while playing at a playground.
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There was no significant past medical history or family history, and his developmental milestones were within normal limits.
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Neurological examination revealed a clear mental status, but the patient complained of nausea and demonstrated reduced visual attention.
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Physical examination showed no external signs of trauma, and his vital signs, including temperature, were within normal ranges.
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Brain computed tomography (CT) was performed for further evaluation.
Quiz
Q1. What is the most likely diagnosis for the well-demarcated low-density lesion identified on the CT scan?
① Chronic subdural hematoma
② Epidermoid cyst
③ Arachnoid cyst
④ Vascular malformation
Explanation: The lesion presents with a well-defined border and CT attenuation similar to cerebrospinal fluid (CSF), which is characteristic of an arachnoid cyst. While chronic subdural hematoma may occur post-trauma, it usually exhibits a crescentic shape with evidence of bleeding and encapsulation.
Q2. Which of the following is not a typical clinical manifestation of an arachnoid cyst?
① Headache
② Seizures
③ Muscle spasms
④ Asymptomatic presentation
Explanation: Arachnoid cysts are often asymptomatic or may cause nonspecific symptoms such as headache, dizziness, or seizures. Focal muscle spasms are not commonly associated with arachnoid cysts and are considered atypical.
Q3. What is the most plausible reason for a previously asymptomatic arachnoid cyst to become symptomatic following trauma?
① Intracystic infection
② Sudden enlargement of the cyst
③ Intracystic hemorrhage
④ CSF leakage due to cyst rupture
Explanation: Trauma may increase the internal pressure of an arachnoid cyst, leading to its expansion and resulting in significant compression of adjacent brain structures, thereby producing symptoms.
Findings and Diagnosis
Radiologic Findings:
-
A well-defined, low-density cystic lesion is observed in the left middle cranial fossa.
-
The lesion demonstrates attenuation similar to CSF on CT imaging.
-
There is evidence of mass effect, with compression of adjacent brain parenchyma.
Final Diagnosis:
Arachnoid cyst in the left middle cranial fossa, symptomatic after minor head trauma.
Differential Diagnosis
-
Chronic Subdural Hematoma
-
Common after trauma; typically crescent-shaped with encapsulated fluid.
-
CT density may be slightly higher or lower than CSF and often has irregular borders.
-
-
Epidermoid Cyst
-
Also appears hypodense but typically more irregular in shape than arachnoid cysts.
-
Shows restricted diffusion on diffusion-weighted MRI (DWI), unlike arachnoid cysts.
-
-
Porencephalic Cyst
-
Often associated with a history of prior brain injury (e.g., infarction, hemorrhage).
-
Communicates directly with the brain parenchyma and is not confined to the arachnoid layer.
-
-
Enlarged Perimesencephalic Subarachnoid Space
-
Bilateral and symmetrical without focal mass effect.
-
Represents a benign anatomic variant rather than a true cystic lesion.
-
Discussion
Post-Traumatic Symptomatic Arachnoid Cyst in the Left Middle Cranial Fossa
Arachnoid cysts are benign, CSF-filled lesions within or beneath the arachnoid membrane. Most are congenital in origin, though acquired forms may result from head trauma, infection, or hemorrhage. In the current case, the patient developed a headache and dizziness following minor trauma, and brain imaging revealed an arachnoid cyst in the left middle cranial fossa.
Although many arachnoid cysts remain asymptomatic, they may become symptomatic following trauma, due to:
-
Acute increase in intracystic pressure
-
Expansion of the cyst
-
Resultant compression of adjacent brain structures
These changes can lead to neurological symptoms, such as headache, nausea, visual disturbances, or even seizures.
Treatment
Treatment decisions are based on clinical symptoms, cyst size, and location:
-
Asymptomatic cysts: Regular monitoring with clinical and imaging follow-up.
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Symptomatic cysts (as in this case): Surgical options include:
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Endoscopic fenestration of the cyst to communicate with the subarachnoid space.
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Cystoperitoneal shunting in cases of recurrence or persistent enlargement.
-
Surgical intervention has shown excellent outcomes in most pediatric cases.
References
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Al-Holou, W. N., Terman, S., Kilburg, C., Garton, H. J. L., Muraszko, K. M., & Maher, C. O. (2010). Prevalence and natural history of arachnoid cysts in children. Journal of Neurosurgery: Pediatrics, 5(6), 578–585. https://doi.org/10.3171/2010.2.PEDS09357
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Helland, C. A., & Wester, K. (2007). A population-based study of intracranial arachnoid cysts: Clinical and neuroimaging findings. Journal of Neurology, Neurosurgery & Psychiatry, 78(10), 1129–1133. https://doi.org/10.1136/jnnp.2006.106435
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Wester, K., & Helland, C. A. (2008). Intracranial arachnoid cysts–not always congenital. World Neurosurgery, 69(4), 493–498. https://doi.org/10.1016/j.wneu.2007.10.059
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Pérez-Domínguez, M., Gutiérrez, A. M., Escribano, J., & Prieto, R. (2020). Endoscopic management of symptomatic arachnoid cysts in children: Long-term follow-up. Child's Nervous System, 36(1), 151–158. https://doi.org/10.1007/s00381-019-04353-w
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Cinalli, G., Spennato, P., Aliberti, F., Trischitta, V., Ruggiero, C., Mirone, G., & Caruso, M. (2006). Endoscopic treatment of arachnoid cysts: A series of 75 pediatric patients. Neurosurgery, 58(4), 765–773. https://doi.org/10.1227/01.NEU.0000209880.15503.B6
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Mandonnet, E., Redjimi, M., Parker, F., & Baron, M. H. (2007). Enlargement of arachnoid cyst after minor head trauma. Journal of Clinical Neuroscience, 14(9), 876–879. https://doi.org/10.1016/j.jocn.2006.05.029
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