What are the radiological findings in cavernoma?

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Radiological Findings in Cavernoma

MRI is the imaging study of choice for cavernoma, demonstrating the characteristic "bull's-eye" or "popcorn" appearance with a reticulated core of mixed signal intensity surrounded by a hypointense hemosiderin rim on T2-weighted sequences. 1

MRI Characteristics

Classic Appearance on Standard Sequences

  • The pathognomonic finding is a reticulated core of mixed signal intensity with a surrounding rim of decreased signal intensity on T2-weighted imaging, representing hemosiderin deposition from repeated hemorrhages 2
  • The "popcorn" morphology reflects various stages of hemorrhage with blood products of different ages, though this classic appearance is only visible in 15-22% of cases 3
  • T1-weighted imaging shows variable signal intensity depending on the age of blood products, with hyperintense signals indicating subacute hemorrhage (methemoglobin) 1, 4
  • The hemosiderin rim appears as a complete or near-complete hypointense border on T2-weighted sequences in only 37% of cases 3

Advanced MRI Sequences

  • T2-weighted gradient-echo imaging or susceptibility-weighted imaging (SWI) is superior to standard spin-echo sequences for detecting cavernomas, particularly smaller lesions and multiple cavernomas not visible on conventional imaging 1, 5
  • Smaller cavernomas appear as "black dots" on gradient-echo sequences due to magnetic susceptibility effects from hemosiderin 2
  • These advanced sequences can reveal additional lesions in patients with multiple cavernomas (15% of cases) or familial forms (50% of familial cases) 1

Hemorrhagic Features

  • Adjacent intramedullary hemorrhage extending away from the lesion is present in 58% of spinal cord cavernomas, appearing as linear or flame-shaped non-edematous signal abnormality 3
  • Acute hemorrhage appears isointense on T1-weighted and hypointense on T2-weighted sequences 4
  • Subacute hemorrhage demonstrates hyperintense signal on both T1- and T2-weighted sequences 4
  • Internal blood-fluid levels are uncommon, seen in only 4% of cases 3

Contrast Enhancement

  • Cavernomas typically show slight heterogeneous enhancement or no enhancement after gadolinium administration 4
  • Contrast may increase conspicuity of associated developmental venous anomalies (DVAs), which occur in 20% of cases 1, 5

CT Findings

Non-Contrast CT

  • Non-contrast CT can demonstrate acute hemorrhage but is less sensitive than MRI for detecting non-hemorrhagic cavernomas 1
  • Cavernomas may appear as faintly hyperdense lesions on non-contrast imaging, often with a suprasellar mass that is spontaneously denser than adjacent brain parenchyma 1, 4
  • Microcalcifications are present in some cases, representing chronic hemorrhage with tissue fibrosis and calcification 1, 4

Contrast-Enhanced CT

  • IV contrast increases conspicuity of associated DVAs but adds limited value for cavernoma detection itself 1

Angiographic Findings

Catheter Angiography

  • Cavernomas are typically angiographically occult due to sluggish blood flow through thin-walled sinusoidal spaces without arteriovenous shunting 1
  • Feeding arteries and draining veins are of normal caliber, distinguishing cavernomas from high-flow vascular malformations 1
  • Only 30% of cavernomas show any abnormal vasculature, typically limited to venous pooling or minimal capillary blush 2
  • Catheter angiography may be used to exclude associated high-flow malformations or to demonstrate associated DVAs, which appear as abnormal venous clusters draining into a single collector on the venous phase 1

CTA and MRA

  • CTA and MRA play limited roles in cavernoma assessment, as these modalities are optimized for high-flow lesions 1
  • MRA is not usually helpful for evaluating cavernomas but may demonstrate associated DVAs 1

Location-Specific Features

Supratentorial Lesions

  • 86% of cavernomas are supratentorial, with 63% measuring less than 1 cm in length 1, 3
  • 78% extend to the cord surface, and 65% cause cord expansion 3
  • 32% have an exophytic component extending beyond the brain parenchyma 3

Deep and Eloquent Locations

  • Deeply situated cavernomas (basal ganglia, thalamus, brainstem) are more likely to bleed than superficial lesions 1
  • Chiasmatic cavernomas present with regular enlargement of the optic chiasm (2.5-3 cm), often with acute or subacute hemorrhage 4

Common Pitfalls and Caveats

  • Do not rely solely on standard MRI sequences—gradient-echo or SWI sequences are essential for detecting multiple lesions and smaller cavernomas that may be missed on spin-echo imaging 1, 2
  • Avoid including the hemosiderin rim in treatment planning for radiosurgery, as it may potentiate radiation effects and increase risk of adverse events 1
  • Be aware that classic imaging features (popcorn morphology, complete hemosiderin rim, blood-fluid levels) are often absent, particularly in smaller lesions or those without recent hemorrhage 3
  • Consider associated DVAs in 20% of cases, as most hemorrhage in DVA patients is attributed to associated cavernomas rather than the DVA itself 1, 5
  • Recognize that cavernomas can develop de novo from microhemorrhages, particularly in familial cases or after cranial irradiation, requiring long-term follow-up imaging 6

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Spinal Cord Cavernous Malformations: MRI Commonly Shows Adjacent Intramedullary Hemorrhage.

Journal of neuroimaging : official journal of the American Society of Neuroimaging, 2020

Research

Cavernous hemangioma of the intracranial optic pathways: CT and MRI.

Journal of computer assisted tomography, 1999

Guideline

Management of Incidentally Found Cavernomas

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

De novo cavernoma developing from an asymptomatic thalamic microhemorrhage.

Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2014

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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