
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Arachnoid cyst surgery
Introduction
Overview
Overview
Treatment for arachnoid cysts occurs when symptoms present themselves. A variety of surgical procedures may be used to decompress (remove pressure from) the cyst.
Surgery
Surgery
- There are a number of approaches in treating arachnoid cysts, the most common are:
- Endoscopic fenestration and removal of the cyst wall (advances in neurosurgical techniques favor fenestration over shunt insertion as the preferred method for initial management).[1]
- Microsurgical fenestration;
- Craniotomy followed by shunting.
- Neuroradiology imaging is needed to assess: location of the cyst and its size;
- It is still a controversy which is the best method, some studies state that the fenestration is associated with more complications[2] while some argue that the endoscopic approach is superior with fewer surgical complications in comparison to craniotomy and shunting,[3]
- Regarding symptoms, endoscopic approach has been preferred with hydrocephalus as this allows more space to execute the surgery.[4]
- Location of the cyst also plays an important role on choosing the approach and possible outcomes:
- Middle cranial fossa: endoscopy is still controversial; microsurgery may be a better option in this location.[4]
- Type I – microsurgical fenestration;
- Type II – endoscopic cystocisternotomy, if it fails: microsurgical fenestration or shunting;
- Type III – endoscopic cystocisternotomy, if it fails: microsurgical fenestration or shunting;
- Suprasellar: usually present with hydrocephalus – endoscopic fenestration is the preferred treatment. Craniotomy is associated with increased morbidity. Endoscopic ventriculocystocisternostomy preferred over ventriculocystostomy.[4]
- Interhemispheric: may be:
- Parasagittal: excision of the cyst;
- Midline: associated with agenesis of the corpus callosum, fenestration is preferred.
- Quadrigeminal:
- Type I – Supratentorial
- Type II – Infratentorial:
- Type III – lateral extension toward the temporal lobe. May present with symptoms such as headaches, vomiting, lethargy, and impairment of upward gaze, macrocrania. If symptomatic, they must be treated
- Endoscopic method is preferred for all of them due to the proximity with the pineal region.[4]
- Middle cranial fossa: endoscopy is still controversial; microsurgery may be a better option in this location.[4]
References
References
- ↑ Pradilla, Gustavo, and George Jallo. “Arachnoid cysts: case series and review of the literature.” Neurosurgical focus 22.2 (2007): 1-4.
- ↑ Choi, Jung Won, et al. “Stricter indications are recommended for fenestration surgery in intracranial arachnoid cysts of children.” Child’s Nervous System 31.1 (2015): 77-86.
- ↑ Lee, Yun Ho, Young Sub Kwon, and Kook Hee Yang. “Multiloculated Hydrocephalus: Open Craniotomy or Endoscopy?.” Journal of Korean Neurosurgical Society 60.3 (2017): 301.
- ↑ 4.0 4.1 4.2 4.3 Mustansir, Fatima, Sanaullah Bashir, and Aneela Darbar. “Management of arachnoid cysts: A comprehensive review.” Cureus 10.4 (2018).
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: José Eduardo Riceto Loyola Junior, M.D.[2]
