MRI Anatomy of the Cerebellum and Its Diverse Imaging Appearances

Drag to rearrange sections
Rich Text Content

Magnetic Resonance Imaging (MRI) is a sophisticated imaging modality that plays a pivotal role in the diagnosis and management of cerebellar pathologies. The cerebellum, Latin for "little brain," is located beneath the occipital lobes and is critical for motor control, balance, and coordination. Its complex anatomy and the variety of pathological processes that can affect it make MRI an invaluable tool. In this article, we will explore the cerebellum's anatomy and its appearance in various MRI sequences, including T1, T2, STIR, FLAIR, and DWI.

MRI Anatomy of the Cerebellum

The cerebellum is divided into two hemispheres connected by the vermis. It consists of a cortex made up of gray matter and an inner region of white matter known as the arbor vitae due to its tree-like appearance on coronal sections. The cerebellum is also divided into three lobes: the anterior, posterior, and flocculonodular, which are responsible for different functions.

T1-Weighted Imaging

On T1-weighted MRI sequences, the cerebellar cortex appears relatively hypointense compared to the white matter. The differentiation between gray and white matter is less pronounced in the cerebellum than in the cerebrum. This sequence provides excellent anatomical detail and is particularly useful for assessing cerebellar atrophy and for identifying masses that may alter the normal architecture.

T2-Weighted Imaging

T2-weighted images provide a higher contrast between cerebellar gray and white matter, with gray matter appearing hypointense and white matter hyperintense. This sequence is sensitive to pathologies such as demyelination, edema, and infarction, which appear hyperintense. It is also useful for detecting small lesions and vascular malformations.

Short Tau Inversion Recovery (STIR)

The STIR sequence is invaluable for suppressing fat signals, making it easier to visualize lesions near the skull base and within the cerebellum. On STIR images, the cerebellar parenchyma has a medium to high signal intensity. Pathological conditions that involve inflammation or edema are highlighted as they appear hyperintense against the suppressed background.

Fluid-Attenuated Inversion Recovery (FLAIR)

FLAIR imaging is a variant of T2-weighted imaging with the cerebrospinal fluid (CSF) signal suppressed. It is particularly adept at identifying lesions adjacent to CSF spaces, which would otherwise be difficult to detect. In the FLAIR sequence, the cerebellum appears similar to T2-weighted images, with the added benefit of improved lesion contrast in the periventricular regions.

Diffusion-Weighted Imaging (DWI)

DWI is sensitive to the molecular motion of water and can indicate pathology in areas of the brain where diffusion is restricted. Acute ischemia, infarction, and abscesses within the cerebellum appear hyperintense on DWI. It is especially useful for early detection of acute stroke.

Pathological Appearances on MRI

Cerebellar pathologies may manifest as atrophy, mass effect, or signal changes within the tissue. For example, cerebellar atrophy is characterized by an increase in cerebellar fissures and a decrease in cerebellar volume. This can be appreciated on both T1 and T2 sequences. Masses, such as tumors or hematomas, can cause a distortion of the normal cerebellar anatomy and may display different characteristics depending on their nature and the MRI sequence used.

Tumors

Primary cerebellar tumors, like astrocytomas and medulloblastomas, have varied appearances. Medulloblastomas are typically hypointense on T1 and hyperintense on T2, with variable enhancement after contrast administration. Astrocytomas usually show a mix of signal intensities due to their heterogeneous composition.

Inflammatory Conditions

Multiple sclerosis plaques can appear as hyperintense lesions on T2/FLAIR images and hypointense on T1 within the cerebellum. In acute disseminated encephalomyelitis (ADEM), there may be widespread, poorly defined hyperintense lesions on T2/FLAIR sequences.

Ischemic Stroke

Acute infarcts are hyperintense on DWI with corresponding hypointensity on the apparent diffusion coefficient (ADC) maps, reflecting restricted diffusion. On T2/FLAIR, the infarcted area becomes hyperintense within a few days.

Hemorrhage

Acute hemorrhage exhibits a hyperintense signal on T1 and a variable signal on T2 depending on the stage of blood product evolution. Chronic hemorrhages may be hypointense on both T1 and T2 sequences due to hemosiderin deposition.

Conclusion

The cerebellum's complex anatomy and the wide range of pathologies that can affect it necessitate a thorough understanding of its appearance across various MRI sequences. These imaging modalities are essential tools for clinicians to accurately diagnose and manage cerebellar diseases.

References

Atlas SW. Magnetic Resonance Imaging of the Brain and Spine. 4th ed. Philadelphia: Lippincott Williams & Wilkins; 2009.

Osborn AG, Salzman KL, Barkovich AJ. Diagnostic Imaging: Brain. 3rd ed. Salt Lake City: Amirsys; 2016.

Rossi A, Martinetti C, Morana G, Severino M, Tortora D. MRI of the Fetal Brain: Normal Development and Cerebral Pathologies. Springer; 2019.

Goyal M, Versnick E, Tuite P, et al. "Evaluation of patients with cerebellar atrophy using T1, T2 and FLAIR MRI sequences." Eur J Radiol. 2004;50(1):10-15.

Loevner LA. "MRI of the Postoperative Cerebellum." Neuroradiology. 2000;42(11):809-821.

Parizel PM, Makkat S, Van Miert E, et al. "Intracranial hemorrhage: principles of CT and MRI interpretation." Eur Radiol. 2001;11(9):1770-1783.

Sener RN. "Diffusion MRI: Apparent Diffusion Coefficient (ADC) values in the normal brain and a classification of brain disorders based on ADC values." Comput Med Imaging Graph. 2001;25(4):299-326.

Waldman AD, Cordes D, Hinshaw DB. "Advances in Imaging of Brain Metabolic and Hemodynamic Function." Annu Rev Biomed Eng. 2004;6:447-74.

Calli C, Kitis O, Yunten N, et al. "Perfusion and diffusion MR imaging in enhancing malignant cerebral tumors." Eur J Radiol. 2006;58(3):394-403.

Tofts PS, editor. Quantitative MRI of the Brain: Measuring Changes Caused by Disease. Wiley; 2003

rich_text    
Drag to rearrange sections
Rich Text Content
rich_text    

Page Comments