(Código CIE-9-CM: 348.0)
Cyst arachnoid, also known as cysts leptomeningeal.
Arachnoid cysts (QA) are benign pathological structures of features that could define as clear fluid filled cavities similar to cerebrospinal fluid (LCR), contained within a membrane indistinguishable histologically healthy arachnoid.
Occur during the division of the arachnoid.
The most accepted hypothesis speaks of changes in the separation of endomenix in the third quarter of the neonatal period. The membrane is endomenix mesenchymal tissue surrounding the neural tube. In the third quarter, when the roof of the fourth ventricle is broken, CSF pressure waves flowing through it, the dissected into two layers and result pial, arachnoid and subarachnoid space. Alterations of this mechanism may lead to the formation of separate cavities that, growth in, form cysts.
Other hypotheses are saying that are secondary to focal brain hypoplasia, in which occupy the space provided or produced by alterations of the secretion of substances from the subarachnoid space to the venous system. Also, to explain the subsequent growth of the cyst were raised various theories; between them, the most accepted, because there are cases where it has been demonstrated in vivo, is the formation of valve mechanisms . Have also been described in the literature sometimes cysts associated with meningeal infections and trauma, called secondary, as opposed to those for which the cause is unknown and suspected congenital malformation, and designated primary.
Really it is intraaracnoideos cysts. When diagnosed at the level of middle fossa were called ” sindrom ” lobe agenesis temporal. (This term is now obsolete).
Others are caused by trauma.
An fracture Simple linear, without immediate complications, can cause the development of an arachnoid cyst, hence the need to maintain a proper monitoring of the evolution of consolidation fracture and an etiologic alert to the onset of neurological symptoms.
Constitute a typical diagnosis of childhood, especially in the first two years of life, which represent approximately 1% of intracranial expansive lesions. The most common locations found in various series are the Sylvian fissure and posterior fossa.
5 by 1000 autopsias.son characteristic lesions in childhood, slightly more common in males.
Also found at the spinal level, although they are rare.
- Cisura de silvio 49%
- APC 11%
- Supracolicular 10%
- Vermiano 9%
- Sellar and suprasellar 9%
- Interhemisférico 5%
- Convexity 4%
- Clivus 3%
Simple cysts: Cell line appear to be capable of secretion CSF. The cysts of the middle fossa speak exclusively of this type
Complex cysts that may also contain neuroglia, epéndimo, and other types of tissue.
The symptoms are variable depending on the filesystem nervous central compress, the most striking are other & shy; focal symptoms with signs of intracranial hypertension, as are headache (head pain), hemiparesis,diplopia (double vision), irritability, mood swings, apathy (emotionless), and impaired intellectual performance.
Trench Media suprasellar with fuzzy supra or infratentorial hydrocephalus hydrocephalus
Epilepsy,headache,hemiparesia HTE,Craneomegalia,late development,loss of visual acuity,precocious puberty HTE,craneomegalia,late development
Most cysts are symptomatic in infancy.
Can be diagnosed by the presence of:
- Symptoms of increased intracranial pressure (Headache, sickness…)
- Sudden deterioration: due to the hemorrhage (en quiste o subdural): pit medial cysts are prone to bleeding due to the increased possibility of rupture of bridging veins; due to rupture of the cyst
- Protrusion in the skull
- Focal neurological signs.
- Incidental finding.
- Hydrocephalus (Probably due to compression of the third ventricle)
- Endocrine symptoms: occurring in a 60%. Includes precocious puberty.
- Visual impairment
- In posterior fossa usually produce nonspecific symptoms such as hearing loss and tinnitus sometimes even difficult to distinguish from Meniere's disease and the most characteristic often cerebellar ataxias.
Are diagnosed primarily by TAC.
The ideal method of diffusion MRI sequences (Maybe it will raise the differential diagnosis with epidermoid cysts or neoplastic hemangioblastomas).
- Cystic astrocytomas.
- Wemer cistern
- Hydatid cyst – Cisticercosis
- Myocardial old crebral
- Hollow Line Media.
Size is recommended to treat only the symptoms that occur regardless of the location and. Treatment is still controversial.
Therapeutic options have endoscopic fenestration or craniotomy into the ventricle or subarachnoid space and the implantation of a shunt.
Probably the best treatment consists in the derivation of cyst peritoneum.
Method Advantages Disadvantages
Aspiration- drill and fast Recurrence
Craniotomy with excision of the quísticay wall fenestration to subarachnoid or ventricular space allows inspection of the cyst and vascular structures. Evita in some cases permanent shunt. Possible re-accumulation and more invasive.
Cystoperitoneal Simple Derivation Procedure Unit Shunt and risks of carrying Shunt.
Dr. J. Sales Llopis
Department of Neurosurgery, University General Hospital of Alicante.