Table of Contents
Definition / general | Essential features | Terminology | ICD coding | Epidemiology | Sites | Pathophysiology | Clinical features | Diagnosis | Radiology description | Radiology images | Case reports | Treatment | Gross description | Microscopic (histologic) description | Microscopic (histologic) images | Virtual slides | Positive stains | Negative stains | Electron microscopy description | Molecular / cytogenetics description | Sample pathology report | Differential diagnosis | Additional references | Board review style question #1 | Board review style answer #1Cite this page: Ahmadian SS. Arachnoid cyst. PathologyOutlines.com website. https://www.pathologyoutlines.com/topic/cnstumorarachnoidcyst.html. Accessed October 2nd, 2023.
Definition / general
- Arachnoid cysts are nonneoplastic, intracranial cerebrospinal fluid (CSF) filled spaces lined with arachnoid membranes (Cureus 2018;10:e2458)
- 1% of intracranial masses (Neurosurgery 1997;41:951)
Essential features
- Nonneoplastic, intracranial CSF filled spaces lined by meningothelial cells and an outer collagenous membrane
- Most primary developmental arachnoid cysts occur in the middle frontal fossa due to the splitting of arachnoid membranes (J Neuropathol Exp Neurol 1981;40:61)
- Meningothelial cells are positive for epithelial membrane antigen (EMA)
Terminology
- Meningeal cyst
Epidemiology
- Arachnoid cysts are classified as primary developmental cysts or secondary cysts (Cureus 2018;10:e2458)
- 50 - 65% of primary developmental cysts present in the middle cranial fossa / Sylvian fissure (Pediatr Neurosurg 1996;25:165)
- Arachnoid cysts in the middle cranial fossa are found more frequently in men than in women (Pediatr Neurosurg 1996;25:165)
Sites
- Arise within both cranial and spinal meninges
- Most are supratentorial and found in the middle fossa (J Neurosurg 2013;118:222)
- Other sites include retrocerebellar, convexity, cerebellopontine angle and spinal cord (J Neurosurg 2013;118:222)
Pathophysiology
- Primary developmental cysts occur due to the splitting of arachnoid membranes in utero, resulting in abnormal collections of cerebrospinal fluid (CSF) (J Neuropathol Exp Neurol 1981;40:61)
- Secondary cysts are less common and often occur after trauma, infection or surgery (Case Rep Orthop 2015;2015:250710)
- Mutation of the FOXC2 gene has been reported in familial forms
Clinical features
- Depends on size and location
- Headaches are the most common symptom (J Neurol Neurosurg Psychiatry 2007;78:1129)
- Other symptoms include hydrocephalus, intracranial hypertension, dizziness, nausea, vomiting, mental status changes, ataxia, seizures and hearing loss (Childs Nerv Syst 2015;31:77)
- Arachnoid cysts can be asymptomatic (Childs Nerv Syst 2015;31:77)
Diagnosis
- Computed tomography (CT) and magnetic resonance imaging (MRI) for radiologic assessment
- Surgical resection is required for a definitive diagnosis
Radiology description
- MRI is the diagnostic procedure of choice
- Arachnoid cysts show low signal intensity on diffusion weighted imaging (DWI) and fluid attenuated inversion recovery (FLAIR) (Tani Girisim Radyol 2003;9:418)
- No enhancement
Radiology images
Case reports
- 22 year old man with a spinal epidural arachnoid cyst (Case Rep Orthop 2015;2015:250710)
- 36 year old woman with a well delineated cystic sellar lesion with suprasellar extension (Einstein (Sao Paulo) 2019;17:eAI4269)
- 45 year old woman with a pontomedullary junction arachnoid cyst (Asian J Neurosurg 2022;17:389)
Treatment
- Surgery if symptomatic
Gross description
- Variable in size; can be very large with mass effects
- Thin, transparent wall with a clear, colorless fluid
- Cyst is distinct from leptomeninges and dura
- Reference: Love: Greenfield's Neuropathology, 9th Edition, 2015
Microscopic (histologic) description
- Cyst wall is composed of a single layer of meningothelial cells and an outer collagenous membrane
- Meningothelial cells often partially denuded and may not always be recognizable
- Rare foci of meningothelial hyperplasia with or without psammoma bodies
- Focal inflammation (rare)
- Reference: Love: Greenfield's Neuropathology, 9th Edition, 2015
Microscopic (histologic) images
Positive stains
- Meningothelial cells are positive for EMA
Negative stains
- Cytokeratin, GFAP, transthyretin and synaptophysin
Electron microscopy description
- Tendency of meningothelial tissues to cleave along the dura - arachnoid interface layer (J Neuropathol Exp Neurol 1979;38:434)
Molecular / cytogenetics description
- Mutation of the FOXC2 gene has been reported in familial forms (PLoS One 2013;8:e80548)
Sample pathology report
- Cyst wall, excision:
- Arachnoid cyst (see comment)
- Comment: The histologic section shows a cystic lesion composed of a single layer of meningothelial cells with an outer layer of delicate fibrous tissue. The meningothelial cells are positive for EMA by immunohistochemistry, which confirms the diagnosis.
Differential diagnosis
- Epidermoid cyst:
- Squamous cyst lining
- Lamellar keratin debris
- Positive for keratin
- Endodermal cyst:
- Pseudostratified epithelium cyst lining with bronchogenic (ciliated) or gastrointestinal (glands) differentiation
- Positive for keratin
- Ependymal cyst:
Additional references
Board review style question #1
Board review style answer #1
B. EMA. The histologic section shows a cystic lesion with a single layer of meningothelial cells with flattened nuclei and delicate fibrous tissue suggestive of an arachnoid cyst. The meningothelial cells are positive for EMA.
Comment Here
Reference: Arachnoid cyst
Comment Here
Reference: Arachnoid cyst