FACTS
A/P
Counseling parents who are often shocked that a large mass like this is just watched, especially when radiology reads talk about shift, mass effect, etc.
- In general, candidates for surgical intervention: patients with clear symptoms of increased ICP that correlate with cyst expansion, such as progressive macrocephaly, papilledema, and progressive cranial neuropathy,
- People (both parents and referring doctors) will be surprised the management is nothing for these, even when they're massive (> 5cm). You need to reassure them this is standard management.
- "What caused this cyst?"
https://ispn.guide/hydrocephalus-and-other-anomalies-of-csf-circulation-in-children/arachnoid-cysts-of-the-head-and-spine-in-children-homepage/complications-of-therapies-for-arachnoid-cysts-of-the-head-and-spine-in-children
No unifying theory for origin: Many theories exist about the origin of arachnoid cysts, including infection, trauma, hydrocephalus, and metabolic derangements, but no unique explanation has been accepted (25).
No unifying theory for origin: Many theories exist about the origin of arachnoid cysts, including infection, trauma, hydrocephalus, and metabolic derangements, but no unique explanation has been accepted (25).
- "Will this cyst keep growing?" Rarely grow after 4 years of age
What are neurosurgical management paradigms for arachnoid cyst?
Useful to know this so you can explain that treatment is not straightforward and complication-laden. Conceptually it's basically like treating "hydro," you need to shunt the fluid whether intracranially (via fenestration into an open basal cistern) or extracranially (i.e. shunt).
Paradigm of treatment | ||
Fenestration - You need to find a way to communicate the cyst with normal cerebrospinal fluid (CSF) pathways of the brain. You basically need to find an open cistern to drain the cyst permanently | • Hemiparesis • CN3 palsies • Hypothalamic injury • ↑ seizure frequency • Surgical Hematomas | • 60% success (lower in infants, up to 90% if no hydro/ventriculomegaly/macrocephaly) • 40-80% will eventually require a shunt |
Shunting if fenestration fails or there is no open cistern to communicate the cyst to. | • infection • malfunction • overdrainage • (the usual) | • 55-100% of middle fossa cysts with hydro/ventriculomegaly will require permanent shunt • small cysts may become obliterated and not require functioning shunt anymore |