Cavernous angioma overview: Difference between revisions
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==Causes== | ==Causes== | ||
There are no established causes for cavernous angioma. | There are no established causes for [[cavernous angioma]]. | ||
==Differentiating Cavernous angioma from other Diseases== | ==Differentiating Cavernous angioma from other Diseases== | ||
Revision as of 09:17, 11 March 2022
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Cavernous angioma Microchapters |
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Diagnosis |
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Treatment |
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Cavernous angioma overview On the Web |
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American Roentgen Ray Society Images of Cavernous angioma overview |
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Risk calculators and risk factors for Cavernous angioma overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Edzel Lorraine Co, DMD, MD
Overview
Cavernous angioma, also known as cerebral cavernous malformation (CCM) or cavernoma, is a rare disease that involves the capillaries of the central nervous system. CCMs have dilated endothelial-lined sinusoidal capillaries which lack intervening neural tissue. This is the only characteristic that can distinguish these lesions from capillary telangiectasia.
CCMs can be classified as sporadic or familial, which has an autosomal dominant form of inheritance. The majority of CCMs are recent and remote hemorrhages. These lesions range in size from millimeters to almost less than 3 centimeters in diameter.
Historical Perspective
Cavernous angioma, also known as cavernous hemangioma, cavernoma, and cerebral cavernous malformation, is a vascular malformation with still an unclear history of its first clinical discovery.
Pathophysiology
Developmental venous anomaly (DVA) can cause a chronic increase in intracranial pressure which can form microhemorrhages around DVA, leading to the development and growth of cavernous angioma. There are two patterns of cavernous angioma, the sporadic and the familial pattern.
Causes
There are no established causes for cavernous angioma.
Differentiating Cavernous angioma from other Diseases
Cavernous angioma appears very similar on MR with calcified neoplastic and hemorrhagic lesions, most especially renal cell carcinoma, melanoma, pleomorphic xanthoastrocytomas, and oligodendrogliomas.
Epidemiology and Demographics
Cavernous angioma is the second most common form of intravascular malformation next to the developmental venous anomaly (DVA). The incidence in the general population is between 0.1–0.5%, and clinical symptoms typically appear between 30 to 50 years of age. Once thought to be strictly congenital, these vascular lesions have been found to occur de novo.
Risk Factors
Family history increases the risk of having cavernous angioma. Genetic testing is recommended for the pathogenic variants of cavernous angioma (KRIT1, MGC4607, and PDCD10).
Natural History, Complications, and Prognosis
Cavernous angioma is usually a benign course since it is a low-flow and low-pressure lesion. Patients with cavernous angioma have variable signs and symptoms, with seizure as the most predominant symptom, followed by hemorrhage and focal neurologic deficit.
Diagnosis
History and Symptoms
CCMs have varying presentations and these can be in the form of hemorrhagic stroke, focal neurological deficits, recurrent headaches, and seizures. Howevever, CCMs can be asymptomatic sometimes.
Physical Examination
Cavernous angioma, also known as cavernous hemangioma, can affect several organs. Diagnosing this condition should be correlated with imaging findings.
CT scan
CT scan is not usually used as a primary modality to diagnose cavernous angiomas due to inablility to detect smaller lesions despite the ability to detect lesions complicated by calcification or hemorrhage.
MRI
Diagnosis is most commonly made accidentally by routine magnetic resonance imaging (MRI) screening, but not all MRI exams are created equal. It is paramount that the patient request a gradient-echo sequence in order to unmask small or punctate lesions which may otherwise remain undetected. These lesions are also more conspicuous on FLAIR imaging compared to standard T2 weighing. FLAIR imaging is different from Gradient sequences, rather, it is similar to T2 weighing but suppresses free-flowing fluid signal. Sometimes quiescent CCMs can be revealed as incidental findings during MRI exams ordered for other reasons.
MRA
Sometimes the lesion appearance imaged by MRI remains inconclusive. Consequently neurosurgeons will order a cerebral angiogram or magnetic resonance angiogram (MRA). Since CCMs are low flow lesions (they are hooked into the venous side of the circulatory system), they will be angiographically occult (invisible). If a lesion is discernible via angiogram in the same location as in the MRI, then an arteriovenous malformation (AVM) becomes the primary concern.
Other Imaging Findings
There are no other imaging findings associated with cavernous angioma.
Other Diagnostic Studies
Diagnostic biomarkers can be utilized too in conjunction with imaging tools to identify cavernous angioma.
Treatment
Surgery
Surgery is the mainstay treatment for cavernous angioma. Complete surgical resection should be done to prevent seizures and hemorrhage due to remnant tissue.
Cost-effectiveness of therapy
Since cavernous angioma can be treated via medical or surgical option, therapy for this condition is relatively cost-effective.
Futures of Investigational Therapies
Several insights on development of cavernous angioma exist. Some drugs have been identified to be able to reduce risk of hemorrhage, and possible development of new lesions. Advances in biomarkers are now being studied more.