Scalp cirsoid aneurysm

Scalp cirsoid aneurysm

They are also referred to as aneurysma serpentinumaneurysm racemosum, or plexiform angioma.

Cirsoid aneurysm of the scalp is one of the rarest occurrences in neurosurgery. It is an aneurysmal tumor formed by arteriovenous fistula of the arteries and veins of the scalp 1)

They can be easily misdiagnosed and mistreated.

Historically their unusual portly appearance led to various synonyms being coined for the entity 2).


Scalp AVM (SAVM) is a rare condition 3) 4) and infrequently encountered by the neurosurgeon 5).


Its origin can be congenital or traumatic.

Congenital arteriovenous malformations (AVMs) of scalp are rare. They are usually not symptomatic at birth and are often misdiagnosed as haemangiomas. To date, only two cases of symptomatic neonatal scalp AVM have been reported in literature. Pathophysiology of congenital AVM is not completely understood but genetic and acquired causes are implicated. Diagnosis and management are often difficult and require multidisciplinary approach. Hussain et al. report a rare case of symptomatic congenital scalp AVM in a 10-day-old neonate who was successfully managed 6).


The clinical picture presents with complaints of increased scalp, scalp disfigurement, pain and neurological symptoms.

They can present a subcutaneous scalp lump or a large, pulsatile mass with a propensity to skin erosion and massive haemorrhage 7) 8).

The symptoms associated with cirsoid aneurysm of scalp vary according to the size of the fistula. Common clinical manifestations include loud bruit, pulsatile scalp mass, headache, and tinnitus. If left untreated, there is an increased risk of developing life-threatening complications such as aneurysmal hemorrhage or scalp necrosis 9) 10) 11).


Since cerebral blood flow may decrease depending on the progression of the lesion, the cerebral blood flow should be evaluated. Considering the treatment modalities depending on the lesion can provide treatment with less recurrence and higher patient satisfaction 12).


Scalp cirsoid aneurysm treatment.


Even after complete surgical resection, a case of recurrence after 18 years has been reported 13), which is why regular follow-up is advised.

Systematic Review

Sofela et al. conducted a PUBMED, SCOPUS, OVID SP, SciELO, and INFORMA search using the keywords; “cirsoid,” “aneurysm,” “arteriovenous,” “malformation,” “scalp,” “vascular,” and “fistula.” They identified 74 pertinent papers, reporting 242 cases in addition to our reported index case.

Median age at presentation was 25 yr (range 1-72 yr); male to female ratio was 2.5:1. The most common symptoms were a pulsatile mass (94% of patients), headaches (25%), and tinnitus (20%). The median duration of symptoms was 3 yr (6 d to 31 yr), with 60.2% occurring spontaneously, 32.23% traumatic, and the rest iatrogenic. A total of 58.5% of cases were managed with surgical excision only, 21.6% with endovascular embolization only, and 14.5% with a combination of both methods. The complication rate observed in the endovascular embolization treatment cohort (55.8%) was significantly higher than that observed in the surgical excision only cohort (9.9%) (P < .00001) and in the combined therapy cohort (0%) (P < .00001). There is a low recurrence rate after treatment irrespective of modality: surgical excision only (6.3%), endovascular embolization only (8.3%), and combined therapy (0%).

Scalp cirsoid aneurysms are associated with good prognoses when recognized and managed appropriately. They suggested combining surgery with endovascular embolization as the optimum treatment modality 14).

Case series

Scalp cirsoid aneurysm case series.

Case reports

Scalp cirsoid aneurysm case reports.

Anterior inferior cerebellar artery aneurysm treatment

Anterior inferior cerebellar artery aneurysm treatment

The management strategies for treatment differ according to the location and configuration of the aneurysm. The existing body of neurosurgical literature contains articles published on aneurysms arising from the AICA near the basilar artery (BA), intracanalicular/meatal aneurysms, and distal AICA. Several therapeutic options exist, encompassing microsurgical and endovascular techniques.

Anterior inferior cerebellar artery aneurysms are rare lesions with a predisposition for distal location and non-saccular morphology. These aneurysms are less amenable to clipping and may instead require aneurysm trapping with bypass.

Anterior inferior cerebellar artery aneurysm endovascular treatment

Anterior inferior cerebellar artery aneurysm surgery

Ophthalmic artery aneurysm

Ophthalmic artery aneurysm

Ophthalmic artery aneurysm” usually refers to a carotid-ophthalmic junction aneurysm 1).

Those that arise from the superomedial aspect of the internal carotid artery just distal to the ophthalmic artery origin and projects superiorly or dorsomedially towards the lateral portion of the optic nerve.

Ophthalmic segment aneurysms (OSAs) OSAs include (NB: nomenclature varies among authors):

1. ophthalmic artery aneurysms.

2. superior hypophyseal artery aneurysms:

a) Paraclinoid internal carotid artery aneurysm: usually does not produce visual symptoms

b) suprasellar variant: when giant, may mimic pituitary tumor on CT.



Clinical features



Case series

Case reports



Drake CG, Vanderlinden RG, Amacher AL. Carotid-ophthalmic aneurysms. J Neurosurg. 1968 Jul;29(1):24-31. PubMed PMID: 5674088.
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