Cavernous Angioma also referred to as cavernous malformations (CMs), cavernous hemangiomas, or cavernomas are a type of intracranial vascular malformation with developmental origin. The terms 'haemangioma' and 'cavernoma' are a misnomer as the lesions are nonneoplastic.
Vascular malformations involve invariably every organ of the body and are grouped into the following four types by their gross and histopathologic characteristics:
Cavernous angiomas occur sporadically or in a familial pattern. Serial MRIs reveal de novo lesions in families with genetic predisposition to cavernous angiomas. The de novo development of CMs after brain biopsy and after radiosurgery also provides substantial evidence for the developmental nature of these lesions. Familial cases show an autosomal dominant pattern of inheritance with incomplete penetrance. There are several reports regarding the hereditary mutations linked to three genetic loci (CCM1, CCM2, and CCM3) which are responsible for familial cerebral cavernous malformations. Approximately all familial cases of cavernous cerebral malformations among Hispanic Americans and non-Hispanic Families have been linked to a founder mutation of CCM1 localized to 7q and CCM2 at 7p and CCM3 at 3q respectively. Furthermore, there is a belief regarding a "second hit mutation" necessary for the onset of the pathology. 
Cavernous angiomas of the brain and spinal cord occur at all ages, but frequently patients present symptomatically occur in the third to sixth decades life. There is no male or female genetic predisposition. Surveys suggest that cerebral cavernous malformation (CCM) is present in 0.5% of the population. However, it tends to become symptomatic in only 40% of the cases. Sporadically occurring malformations are usually solitary and tend to remain asymptomatic. Whereas familial CCMs are multiple in number and disposed to become symptomatic. Screening of family members is therefore indicated. Although the majority of CCMs are diagnosed in adults, 25% of cases have been found in children.
Familial multiple cavernous malformation syndromes are where the number of multiple lesions is typically 5 or more, and suffering individuals usually present with seizures and/or focal neurological deficits due to recurrent hemorrhages.
Grossly, cavernous malformations have a characteristic "mulberry" appearance with engorged purplish clusters of vessels. The diameter varies from 2 mm to several centimeters.
On microscopic examination, the cavernous angiomas consist of dilated, thin-walled capillaries with a simple endothelial lining and a thin, fibrous adventitia. Vessel walls lack elastic fibers and smooth muscles. The classic description of cavernous angiomas states no intervening brain tissue in between the vascular channels of the lesion. However, further studies noted intervening brain parenchyma in 70 percent of the lesions. The closely surrounding tissue is gliotic and hemosiderin-laden due to previous hemorrhages. It also contains dilated capillaries that may represent telangiectasias. Inflammation, calcification and, rarely, ossification can be found, usually in larger lesions. Developmental venous anomalies (DVAs) are also associated with cavernous malformations (10-20%) more often with lesions present in the posterior fossa than in the supratentorial compartment. A mixed vascular malformation (MVM) is a term used to describe the anomaly comprising of a developmental venous anomaly and a cavernous malformation.
As earlier mentioned the majority of lesions remain asymptomatic throughout life while others present with a headache, seizure or focal neurological deficit due to hemorrhage. The risk of hemorrhage is more for familial versus sporadic cases. The bleeding tendency is also documented more with CMs that are associated with DVAs or atypical venous drainage. The presentation of cavernous malformations CMs is dependent on their location.
CT scanning plays only a limited role largely because of its relative lack of specificity. On nonenhanced, CT scan cavernomas may or may not be apparent.If visualized they usually appear as focal oval or nodular lesions with mild-to-moderate increased attenuation. Lack of mass effect on the surrounding brain parenchyma is common unless a recent hemorrhage is present. CT scan demonstrates calcification in 33% of cavernomas. Surrounding mantle of edema is usually apparent if there is a hemorrhage. Older lesions can contain central hypoattenuating non-enhancing areas or cystic cavities from reabsorbed old hematomas. Contrast enhancement can vary from minimal to prominent. Some studies report 70-94% of cavernous angiomas to demonstrate mild-to-moderate post contrast enhancement which usually has a mottled or heterogeneous appearance. The peripheral rim of decreased attenuation is because of the pseudo capsule of gliotic tissue. Hemorrhagic events particularly those found in relatively young patients ought to be characterized further, and cavernous angioma should be considered among the possible etiologies. Also because of their propensity to act as an epileptogenic focus CMs should always be considered in the workup of a patient with a seizure disorder, especially if the patient is aged 20-40 years.
MRI establishes the diagnosis. It demonstrates typical, smoothly circumscribed lesions with popcorn like, mulberry like the pattern of variable signal intensities which are consistent with hemorrhage in various stages of evolution. The heterogeneous core typically is surrounded completely by a low-signal-intensity hemosiderin rim which is most apparent, or blooms, on T2-weighted and gradient-recalled images. Smaller cavernous angiomas are usually not apparent on conventional spin echo sequences, and these smaller lesions are best-depicted Gradient echo or T2* sequences, or other susceptibility weighted images (SWI). SWI imaging also plays an important role in identifying the number of lesions in patients with familial or multiple cavernous angiomas. SWI also has high sensitivity in detecting calcification.
If a recent bleed has occurred then surrounding edema or mass effect may be present. The lesions show a variable pattern of enhancement. Contrast enhanced images help delineate any potential associated developmental venous anomalies. This is critical for preoperative surgical planning as the un-deliberate resection of DVAs may compromise normal cortical venous drainage and thus lead to brain venous infarction. Angiographically these lesions are occult and usually show nonspecific findings like capillary blush or early draining vein.
Conservative approach is observed for asymptomatic CMs, irrespective of location. Serial routine MRIs are carried out to monitor the changes in the lesion. The conservative approach is continued for as long as the lesion appears stable, with no additional symptoms or evidence of hemorrhage.
Most cavernomas are supratentorial, and indications for resection include progressive neurological deficit, intractable epilepsy, or a single hemorrhage in CMs when located in a noneloquent area. Surgical resection of symptomatic CM lesions is considered in the case of multiple hemorrhages in eloquent areas that are associated with deteriorating neurological deficits. Other indications include severe symptoms, such as cardiac or respiratory instability, and the presence of a CM lesion within 2 mm from the pial surface. Several studies report excellent surgical outcomes (70-97 percent) for cerebral and cerebellar cavernous angiomas. Furthermore, the use of stereotaxy and intraoperative functional MR imaging combined with surgical microdissection has significantly reduced the risk of complications for most supratentorial CM lesions.
Brain stem cavernomas pose particular problems to surgical approach due to the tightly packed nuclei and nerve fibers. Therefore, any additional mass or introduction of fluid, such as blood products from a bleed, can compress or crush important nerve fibers that control basic, involuntary functions like respiration or heart beat.Surgical removal may be considered in any of the below-mentioned cases:
Cavernous angioma may not be diagnosed when it presents as acute intracerebral hematoma on nonenhanced CT or MR images. Post contrast enhancement scan reveals cavernous angiomas as areas of nodular enhancement adjacent to the hematoma. Elliptical rather than round shape and loss of brain volume are evidence supporting pure intracerebral hematoma from the underlying cavernoma.
The differential, when cavernous venous malformations are numerous, is that of other causes of cerebral microhemorrhages:
The diagnosis and management of brain cavernous hemangioma is not always simple and is best done with a multidisciplinary team that includes a radiologist, neurologist, neurosurgeon, and a pathologist. The patient may first present to the primary care provider or nurse practitioner with CNS symptoms, depending on the location. The management of these lesions is best left to the neurosurgeon. Asymptomatic lesions can be observed but symptomatic lesions need some type of surgery. Depending on their location, complications from surgery are not uncommon. The prognosis for symptomatic patients who undergo surgery is guarded as a number of them are left with permanent neurological deficits.  (Level V)
|||Khattar NK,Adams SW,Schaber AS,White AC,Al Ghamdi M,Hruska RT,Savage JJ,Downs RK,Hattab EM,Williams BJ, Endoscopic Endonasal Surgery for the Resection of a Cavernous Hemangioma with a Sellar Extension. Cureus. 2018 Nov 30; [PubMed PMID: 30740283]|
|||Li H,Zhang B,Wang W,Wei MH,Liu BY,Wu Z, The clinical features,intradural transcavernous surgical management and outcomes of giant cavernous sinus hemangiomas:a single-institutional experiences. World neurosurgery. 2019 Feb 5; [PubMed PMID: 30735865]|
|||Pandey SK,Mani SE,Sudhakar SV,Panwar J,Joseph BV,Rajshekhar V, Reliability of Imaging-Based Diagnosis of Lateral Ventricular Masses in Children. World neurosurgery. 2019 Jan 17; [PubMed PMID: 30660880]|
|||Li W,Sun Q,Duan X,Yi F,Zhou Y,Hu Y,Yao L,Xu H,Zhou L, [Etiologies and risk factors for young people with intracerebral hemorrhage]. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences. 2018 Nov 28; [PubMed PMID: 30643071]|
|||Villalonga JF,Saenz A,Campero A, Surgical treatment of an asymptomatic giant supratentorial cavernous hemangioma. Case report. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 2019 Jan 4; [PubMed PMID: 30616875]|
|||Apra C,Dumot C,Bourdillon P,Pelissou-Guyotat I, Could propranolol be beneficial in adult cerebral cavernous malformations? Neurosurgical review. 2019 Jan 4; [PubMed PMID: 30610500]|
|||Li ZH,Wu Z,Zhang JT,Zhang LW, Surgical Management and Outcomes of Cavernous Sinus Hemangiomas: A Single-Institution Series of 47 Patients. World neurosurgery. 2019 Feb; [PubMed PMID: 30447442]|
|||Pesce A,Frati A,D'Andrea G,Palmieri M,Familiari P,Cimatti M,Valente D,Raco A, The Real Impact of an Intraoperative Magnetic Resonance Imaging-Equipped Operative Theatre in Neurovascular Surgery: The Sapienza University Experience. World neurosurgery. 2018 Dec; [PubMed PMID: 30165208]|
|||Zacà D,Corsini F,Rozzanigo U,Dallabona M,Avesani P,Annicchiarico L,Zigiotto L,Faraca G,Chioffi F,Jovicich J,Sarubbo S, Whole-Brain Network Connectivity Underlying the Human Speech Articulation as Emerged Integrating Direct Electric Stimulation, Resting State fMRI and Tractography. Frontiers in human neuroscience. 2018; [PubMed PMID: 30364298]|
|||Tang X,Li M,Xu Y,Xu M,Sun W,Li G,Xu N,Wang L, TMS-induced motor evoked potential in the preliminary diagnosis of intracranial cavernous hemangioma: A case report. Brain stimulation. 2018 Nov - Dec; [PubMed PMID: 30087033]|
|||Lee CC,Chou CL,Chen CJ,Yang HC,Wu HM,Shiau CY,Pan DH,Chung WY, Stereotactic radiosurgery for hypervascular intracranial tumors. Journal of neuro-oncology. 2018 Dec; [PubMed PMID: 30128688]|
|||Xie MG,Xiao XR,Guo FZ,Zhang JT,Wu Z,Zhang LW, Surgical Management and Functional Outcomes of Cavernous Malformations Involving the Medulla Oblongata. World neurosurgery. 2018 Nov; [PubMed PMID: 30077748]|
|||Barbagallo GMV,Morrone A,Certo F, Intraoperative Computed Tomography and Awake Craniotomy: A Useful and Safe Combination in Brain Surgery. World neurosurgery. 2018 Nov; [PubMed PMID: 30031198]|
|||Xie MG,Xiao XR,Li D,Guo FZ,Zhang JT,Wu Z,Zhang LW, Surgical Treatment of the Medullary Cavernous Malformations: 53 Cases. World neurosurgery. 2018 Oct; [PubMed PMID: 29981463]|