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(Left) Sagittal T1WI MR shows caudal descent of the cerebellar tissue and 4th ventricle ſt associated with callosal dysgenesis st. Abnormal tectum, or beaking ﬇, is an important associated
Differential Diagnosis
finding. (Right) Sagittal T1WI C+ MR demonstrates a homogeneously enhancing meningioma with conspicuous dural "tails" ſt along the anterior margin of the foramen magnum.
(Left) Sagittal T2WI MR reveals a large amount of rheumatoid pannus ſt with effacement of the spinal canal and posterior displacement of the lower medulla. The odontoid process is abnormally "pointed" and eroded ﬇. (Right) Axial T2WI MR shows a jugular foramen schwannoma with a very large cisternal component ﬇ displacing the medulla and filling the basal cistern. Note that the left jugular foramen is filled by a schwannoma ſt.
Foramen Magnum Mass
Chiari 2 Malformation Meningioma, Clivus
Rheumatoid Arthritis, Adult Schwannoma, Jugular Foramen
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Chordoma, Clivus Chordoma, Clivus
(Left) Sagittal T1WI C+ MR
shows a very large enhancing chordoma of the clivus with involvement of the sphenoid sinus ſt and C2 vertebra ﬇ with extension into the posterior fossa and foramen magnum st. (Right) Sagittal T1WI FS MR reveals a hyperintense midline chordoma arising from the inferior clivus, projecting anteriorly into the nasopharynx ſt and posteriorly into the foramen magnum ﬇. Note the medullary compression st.
Foramen Magnum Mass
Calcium Pyrophosphate Dihydrate
Ependymoma
Fusiform Aneurysm, ASVD Fusiform Aneurysm, Non-ASVD
Deposition Disease (CPPD)
Differential Diagnosis
(Left) Sagittal T1WI C+ MR shows an enhancing ependymoma ſt projecting from the inferior 4th ventricle into the superior foramen magnum ﬇. (Right) Sagittal T2WI MR shows CPPD involvement of the upper cervical spine with an associated low-signal mass ſt compressing the lower medulla ﬇. Pseudopannus is nonspecific with differential diagnoses that include degenerative arthritis, calcium pyrophosphate dihydrate deposition disease, and gout.
(Left) Sagittal T1WI MR shows a mixed signal intensity extraaxial mass ſt. An extraaxial lesion with evidence of flow and thrombosis is strongly suggestive of aneurysm. Only small residual flow voids are seen on this sagittal image st. (Right) Sagittal MRA depicts a fusiform nonatherosclerotic aneurysm of the basilar artery in an adolescent male. The vessel wall is somewhat irregular ſt but without stenosis.
Brainstem Glioma, Pediatric Neurenteric Cyst
(Left) Sagittal T1WI MR shows
a markedly expanded upper cervical cord ſt, medulla ﬇, and inferior pons st resulting from an infiltrative mass isointense to the brainstem. Brainstem gliomas often smoothly enlarge the brainstem. (Right) Sagittal T1WI C+ MR shows an extraaxial mass ſt in the anterior foramen magnum elevating and displacing the medulla. This neurenteric cyst is slightly hyperintense compared to cerebrospinal fluid and was conspicuous on FLAIR (not shown).
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SECTION 13
Peripheral Nerve and Plexus
Normal Plexus and Nerve Anatomy 414 Superior Sulcus Tumor Thoracic Outlet Syndrome Muscle Denervation Brachial Plexus Traction Injury Idiopathic Brachial Plexus Neuritis 422 Traumatic Neuroma Radiation Plexopathy Peripheral Nerve Sheath Tumor Peripheral Neurolymphomatosis Hypertrophic Neuropathy 427 Femoral Neuropathy Ulnar Neuropathy Suprascapular Neuropathy Median Neuropathy Common Peroneal Neuropathy 432 Tibial Neuropathy
418 419 420 421
423 424 425 426
428 429 430 431
433
Normal Plexus and Nerve Anatomy

Terminology

Nerve rootlets: Individual neural filaments of dorsal and
ventral roots directly exiting from spinal cord
Nerve roots: Composed of multiple individual dorsal or ventral nerve rootlets
• Dorsal sensory roots exit from dorsolateral cord and have cell bodies within dorsal root ganglion (DRG)
• Ventral motor roots arise from anterior cord gray matter and have cell bodies within cord
DRG: Dorsal nerve root sensory ganglion, resides in neural
Peripheral Nerve and Plexus
foramen
Spinal nerve (proper): Union of dorsal and ventral nerve roots
• 31 nerve pairs (8 cervical, 12 thoracic, 5 lumbar, 5 sacral, and 1 coccygeal)
• Proper spinal nerve is short in length, bifurcates into ventral and dorsal rami
Ramus: 1st spinal nerve branch
• Larger ventral primary ramus supplies ventral musculature and facets
• Smaller dorsal primary ramus supplies paraspinal muscles and part of facet
Peripheral nerve: Combination of 1 or more rami into single neural conduit
Plexus: Neural network of anastomosing nerves

Imaging Anatomy

Cervical Plexus
The cervical plexus forms from the ventral rami of C1-C4 and, variably, a C5 minor branch. It has ascending superficial, descending superficial, and deep branches that supply nuchal muscles, the diaphragm, and cutaneous head/neck tissues.
Brachial Plexus
The brachial plexus (BP) forms from the ventral rami of C5-T1 and variably from minor branches of C4 or T2. The BP contributes to several nerves originating above the BP proper, including the dorsal scapular nerve, long thoracic nerve, nerves to scalene/longus colli muscles, and a branch to the phrenic nerve. The remaining minor and all major terminal nerve branches arise from the BP proper. Depending on the cranial or caudal variation of the nerves supplying the BP, it can be defined as prefixed or postfixed. A prefixed BP has a large contribution from C4 with or without a small contribution from T1. A postfixed BP has a large contribution from T2 and little to no communication with C5.
Anatomically, the BP is classically divided sequentially (proximal to distal) into 5 segments: Roots/rami, trunks, divisions, cords, and terminal branches. The roots/rami originate directly from the spinal cord levels C5 to T1. The 3 trunks include the superior or upper (C5-C6), middle (C7), and inferior or lower (C8, T1) trunks. Important minor nerves arising directly from the trunks include the suprascapular nerve and nerve to subclavius muscle. Two divisions are described: Anterior division innervates anterior (flexor) muscles and posterior division innervates posterior (extensor) muscles. No named minor nerves arise directly from the anterior or posterior divisions. The 3 cords include the lateral cord (anterior divisions of superior, middle trunks) that innervates anterior (flexor) muscles, the medial cord (anterior division of inferior trunk) that innervates anterior (flexor) muscles, and the posterior cord (posterior divisions of all 3
414
trunks) that innervates posterior (extensor) muscles. The cords branch to form several important named terminal peripheral nerve branches.
Clinically, the BP is divided into 3 discrete segments based on anatomic relationship to the clavicle. These include the supraclavicular (roots, trunks), retroclavicular (divisions), and infraclavicular (cords, terminal branches) plexus.
Lumbar Plexus
The lumbar plexus derives from the L1-L4 ventral rami and a minor branch from T12. Important named minor nerve branches include the iliohypogastric, ilioinguinal, genitofemoral, lateral femoral cutaneous (L2-L3), and superior (L4-S1) and inferior (L5-S2) gluteal nerves. Important major nerve branches include the femoral (posterior division L2-L4) and obturator (anterior division L2-L4) nerves (Table 2).
Lumbosacral Trunk
The lumbosacral trunk (LST) is derived from the ventral rami of L4 (minor branch) and L5, and it is easily followed on axial imaging as it transits along the ventral surface of the sacral ala to join the sacral plexus in the pelvis.
Sacral Plexus
The sacral plexus is composed of the LST, S1-S3 ventral rami, and a minor branch from S4. The sacral rami and LST converge into the upper sacral neural band (LST and S1-S3) that forms the sciatic nerve and the lower sacral neural band (S3-S4) that forms the pudendal nerve.
Coccygeal Plexus
The coccygeal plexus converges from the S5 ventral ramus, Cx1, and a minor branch of S4. The major named branch is the anococcygeal nerve.

Anatomy-Based Imaging Issues

Normal Nerve Findings
Surrounding perineural fat provides excellent visualization of nerves and allows them to be easily distinguished from adjacent soft tissues. The normal peripheral nerve is a round/ovoid shape with well-defined internal fascicular architecture. Normal nerve fascicles are uniform in size and shape, and this characteristic fascicular pattern helps distinguish peripheral nerves from other lesions, such as schwannoma or a ganglion cyst, which also demonstrate high intrinsic T2 signal intensity.
Intrafascicular signal intensity is determined predominately by endoneurial fluid and axoplasmic water, whereas the interfascicular signal is dominated by fibrofatty connective tissue that is amenable to fat suppression. Therefore, normal nerve fascicles are isointense to adjacent muscle tissue on T1WI and mildly hyperintense relative to muscle interspersed within hypointense fibrofatty connective tissue on fat­saturated T2WI or STIR MR. No abrupt change in nerve caliber or course should be observed in an anatomically normal nerve.
Abnormal Nerve Findings
The acutely abnormal nerve demonstrates 1 or more of the following findings: Segmental nerve enlargement, disruption of nerve anatomic continuity, T2 signal intensity approaching that of regional blood vessels on fat-saturated T2WI or STIR sequences, or disruption or distortion of normal fascicular architecture. Entrapped or scarred nerves may show abrupt change in caliber or course.
The abnormal nerve, therefore, remains isointense on T1WI but becomes increasingly hyperintense to muscle on T2WI. In
Normal Plexus and Nerve Anatomy
the setting of injury, it is postulated that increased endoneurial free water content alters the normal signal characteristics of peripheral nerves. The cause of abnormal high signal on T2WI and STIR sequences is not definitively known, but it has been speculated that edema from increased endoneurial fluid due to disordered endoneurial fluid flow or local venous obstruction may explain abnormal T2 hyperintensity. Alterations in axoplasmic flow may also produce increased signal. Axoplasmic flow is impeded by nerve compression, and increased axoplasm proximal and distal to the injury site may produce T2 hyperintensity.
Imaging Pitfalls
It can sometimes be difficult to distinguish peripheral nerve from adjacent vascular structures, particularly if the abnormal nerve displays high T2 signal intensity. Vessels demonstrate internal flow voids, branch at large angles, and show intense contrast enhancement. On the other hand, nerves do not show flow voids, branch at relatively acute angles, enhance minimally, and display a discrete distinctive fascicular architecture on transverse imaging.

Clinical Implications

High-resolution MR technique readily identifies the large major nerves and major plexi and permits visualization of their internal neural anatomy. Conversely, smaller major and essentially all minor peripheral nerves are too small to directly visualize.
Successful peripheral nerve imaging requires a strong working knowledge of normal plexus and nerve anatomy. Additionally, peripheral nerve imaging is time consuming and necessitates constraining the imaging volume to clinically relevant regions rather than general "screening" surveys. It is critical to have all pertinent clinical and electrodiagnostic data available to appropriately constrain imaging volume and help detect subtle abnormalities.

Differential Diagnosis

Normal Nerve/Plexus
The normal nerve/plexus shows normal course, caliber, contour, and internal fascicular architecture. Consider myopathic or other nonneural etiology in symptomatic patients.
Nerve/Plexus Mass
Neural neoplasms are most commonly of neural sheath origin. Consider solitary or plexiform neurofibroma, schwannoma, or malignant peripheral nerve sheath tumor. Less common considerations include neurolymphomatosis and peripheral nerve metastasis.
Trauma
Etiologies include traction (stretch or avulsion), laceration (projectile, fracture fragment, sharp object), or direct compression (hematoma, fracture).
MR is sensitive for the detection, and in some cases, discrimination of all 3 described peripheral nerve injury levels. Neurapraxia, the least severe type of injury, is characterized by focal damage to the myelin sheath without axonal disruption and manifests as identifiable but swollen and hyperintense nerve fascicles. Axonotmesis is an intermediate level of crush or traction injury that produces axonal disruption and subsequent wallerian degeneration but leaves the Schwann cells and endoneurium intact. Axonotmesis will display a homogeneously increased signal intensity nerve with
Peripheral Nerve and Plexus
loss of fascicular architecture at the injury site. Neurotmesis, the most severe form of nerve injury, cannot always be distinguished from axonotmesis in the cases of functional rather than anatomical transaction but may display axonal disruption with discontinuity of some or all of the surrounding connective tissues and subsequent wallerian degeneration in definitive cases.
Entrapment Syndrome
Neural compression occurs at characteristic locations. These injuries are often, but not always, related to poor ergonomics or overuse injuries.
Hereditary Motor and Sensory Neuropathy
Inherited peripheral nerve disorders are characterized by abnormally enlarged peripheral nerves (usually palpable if not deep) and variable clinical neuropathy presentations. Some demonstrate the characteristic onion bulb appearance on micropathology following nerve biopsy, reflecting recurrent episodes of demyelination and remyelination. The most common hereditary motor and sensory neuropathy disorder is Charcot-Marie-Tooth, which has characteristic clinical manifestations and may involve the cauda equina, peripheral nerves, or both.
Infection/Inflammation
Myriad pathological etiologies and clinical manifestations characterize this diverse group of disorders. Important causes include syphilis (tabes dorsalis), leprosy, infectious neuritis (usually viral), and sarcoidosis. Immune-mediated noninfectious disorders include postviral or vaccination (Guillain-Barré syndrome), chronic immune demyelinating polyneuropathy, and idiopathic brachial plexitis (Parsonage­Turner syndrome).
Drug/Toxic Injury
Neural injuries have been linked to vinca alkaloids, therapeutic gold, amiodarone, dapsone, thalidomide, and lead or mercury intoxication.
Vascular Insult
Injury may result from either nerve ischemia related to peripheral vascular disease or vascular trauma or sequelae of vasculitis. The most common vasculitis etiologies are diabetes, Churg-Strauss, polyarteritis nodosa, and Wegener granulomatosis.

Selected References

1. Chhabra A et al: Peripheral nerve injury grading simplified on MR neurography: as referenced to Seddon and Sunderland classifications. Indian J Radiol Imaging. 24(3):217-24, 2014
2. Crush AB et al: Malignant involvement of the peripheral nervous system in patients with cancer: multimodality imaging and pathologic correlation. Radiographics. 34(7):1987-2007, 2014
3. Demehri S et al: Conventional and functional MR imaging of peripheral nerve sheath tumors: initial experience. AJNR Am J Neuroradiol. 35(8):1615­20, 2014
4. Pham M et al: Peripheral nerves and plexus: imaging by MR-neurography and high-resolution ultrasound. Curr Opin Neurol. 27(4):370-9, 2014
5. Sureka J et al: MRI of brachial plexopathies. Clin Radiol. 64(2):208-18, 2009
6. Bowen BC et al: Plexopathy. AJNR Am J Neuroradiol. 29(2):400-2, 2008
7. Hof JJ et al: What's new in MRI of peripheral nerve entrapment? Neurosurg Clin N Am. 19(4):583-95, vi, 2008
8. Kim S et al: Role of magnetic resonance imaging in entrapment and compressive neuropathy--what, where, and how to see the peripheral nerves on the musculoskeletal magnetic resonance image: part 2. Upper extremity. Eur Radiol. 17(2):509-22, 2007
9. Castillo M: Imaging the anatomy of the brachial plexus: review and self­assessment module. AJR Am J Roentgenol. 185(6 Suppl):S196-204, 2005
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Normal Plexus and Nerve Anatomy
Brachial Plexus Major Nerves
Nerve Definition Motor/Sensory Innervation Important Branches
Radial nerve Terminal branch of posterior
brachial plexus cord
Median nerve Terminal branch arises from both
lateral and medial brachial plexus cords
Ulnar nerve Terminal branch of medial
Peripheral Nerve and Plexus
Musculocutaneous nerve Terminal branch of lateral brachial
Axillary nerve Terminal branch of posterior
brachial plexus cord
plexus cord
brachial plexus cord
Lumbosacral Plexus Major Nerves
Nerve Definition Motor/Sensory Innervation
Obturator nerve Terminal branch of lumbar plexus (anterior
division)
Femoral nerve Terminal branch of lumbar plexus (posterior
division)
Sciatic nerve Largest peripheral nerve branch of sacral plexus Innervates posterior thigh (biceps femoris, semitendinosus,
Common peroneal nerve Major anterior terminal branch of sciatic nerve Innervates anterior leg muscles; superficial peroneal nerve
Tibial nerve Major posterior branch of sciatic nerve Innervates posterior leg muscles (gastrocnemius, soleus, tibialis
Innervates extensor muscles of arm and forearm (triceps, brachioradialis, extensor forearm muscles)
Innervates flexor muscles of forearm and thumb as well as 1st and 2nd lumbricals
Innervates flexor carpi ulnaris, 3rd and 4th lumbricals, and majority of intrinsic hand muscles
Innervates flexor muscles of arm (coracobrachialis, biceps, and brachialis)
Innervates deltoid and teres minor muscles
Innervates thigh adductor muscles
Innervates iliacus, psoas, and quadriceps muscles
semimembranosus, adductor magnus) and all leg muscles (via tibial and common peroneal nerve)
innervates peroneus muscles, extensor digitorum brevis; deep peroneal nerve innervates tibialis anterior, extensor digitorum longus, extensor hallucis longus muscles
posterior, flexor digitorum longus, flexor hallicus longus)
Most important branch is posterior interosseous nerve
Most important branch is anterior interosseous nerve
High-Resolution MR Protocols
MR Pulse Sequence Technical Parameters Technical Comments
Coronal T1WI MR 3- to 4-mm slice thickness, 20- to 24-cm FOV, no
interslice gap
Coronal fat-saturated T2WI or STIR MR 3- to 4-mm slice thickness, 20- to 24-cm FOV, no
interslice gap
Direct axial or sagittal oblique T1WI MR 5- to 7-mm slice thickness, 16- to 20-cm FOV, no
interslice gap
Direct axial or sagittal oblique fat-saturated T2WI or STIR MR
Coronal and axial fat-saturated T1WI C+ MR (optional)
5- to 7-mm slice thickness, 16- to 20-cm FOV, no interslice gap
Same planes as unenhanced imaging sequences Use if suspected or confirmed mass or
Direct coronal plane, not oblique
Direct coronal plane, not oblique
Sagittal oblique plane oriented perpendicular to plexus
Sagittal oblique plane oriented perpendicular to plexus
infection
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Normal Plexus and Nerve Anatomy
Peripheral Nerve and Plexus
(Left) Axial graphic of the thoracic spine shows formation of a typical spinal nerve from dorsal and ventral rootlets to form the spinal nerve proper ſt. The short spinal nerve bifurcates into large ventral ﬇ and small dorsal primary rami st. (Right) Coronal graphic shows the classic anatomic classification of the 5 brachial plexus sections from proximal to distal: Roots ſt (technically ventral primary rami) of C5-T1, trunks ﬇, divisions st, cords ﬈, and terminal major branches ﬊ are shown.
(Left) Coronal STIR MR of the upper right brachial plexus depicts normal mildly hyperintense brachial plexus roots/rami of C5 to T1. C5 and C6 form the superior (upper) trunk ſt, C7 the middle trunk ﬇, and C8 and T1 the inferior (lower) trunk st. (Right) Coronal STIR MR of the lower right brachial plexus demonstrates normal C7, C8, and T1 roots/rami ſt sequentially forming trunks, divisions, and cords. The normal brachial plexus courses retroclavicular into the axilla.
(Left) Sagittal oblique STIR MR demonstrates the ventral primary rami ſt of C5 through T1 proximal to the trunks. C8 exits above the 1st rib ﬇, whereas T1 exits below. The brachial plexus is "sandwiched" between the anterior and middle scalene muscles st. (Right) Sagittal oblique STIR MR distal to the root level shows formation of the upper, middle, and lower trunks ſt arranged in a vertical line between the scalene muscles.
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Superior Sulcus Tumor
KEY FACTS
TERMINOLOGY
• Synonym: Pancoast tumor
• Benign or malignant neoplasm extending to superior thoracic inlet with (1) severe shoulder/arm pain along C8, T1, T2 nerve trunks, (2) Horner syndrome, and (3) weakness + atrophy of intrinsic hand muscles (Pancoast syndrome)
IMAGING
• Soft tissue apical lung mass with variable extension into
Peripheral Nerve and Plexus
chest wall, adjacent bone destruction, brachial plexus invasion
TOP DIFFERENTIAL DIAGNOSES
• Metastatic disease
• Other thoracic tumors (besides non-small cell lung carcinoma)
• Brachial plexus neural tumors
• Hematologic neoplasms
• Radiation fibrosis
(Left) Coronal STIR MR of a patient with non-small cell lung carcinoma, arm pain, and weakness shows extensive architectural distortion of the lung apex by a peripheral lung mass ſt with extension along the brachial plexus elements ﬇. (Right) Coronal T1 C+ FS MR of the same patient demonstrates a heterogeneously enhancing apical lung neoplasm ſt with tumor extension ﬇ along the lower brachial plexus elements.
• Vascular (venolymphatic) malformation
• Infection
PATHOLOGY
• Bronchogenic carcinomas may arise from either upper lobe
• Invades parietal pleura, endothoracic fascia, subclavian vessels, brachial plexus, vertebral bodies, and upper ribs
• Non-small cell lung carcinoma most frequent etiology
CLINICAL ISSUES
• Clinical findings determined by tumor location relative to scalene muscles
• Severe shoulder and arm pain
• Pulmonary symptoms uncommon early in disease course
DIAGNOSTIC CHECKLIST
• Apical lung mass with bone destruction = bronchogenic carcinoma until proven otherwise
• Rare benign tumors or infection may mimic lung carcinoma
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(Left) Axial CECT demonstrates a soft tissue mass ſt involving the right upper lobe with extension beyond the chest wall, producing destruction of the right T1, T2 ribs st. (Right) Axial PET (FDG) CT fusion image reveals marked hypermetabolic radiotracer uptake within the right upper lobe bronchogenic carcinoma ſt.
Thoracic Outlet Syndrome
KEY FACTS
Peripheral Nerve and Plexus
TERMINOLOGY
• Neural, venous, &/or arterial compressive syndrome at thoracic outlet
• Diagnosis made by 1 of 3 methods (by event, affected structure, or compression cause)
IMAGING
• ± cervical rib, elongated C7 transverse process
• ± brachial plexus compression/distortion, scalene muscle inflammation, abnormal vascular flow voids at thoracic outlet
• Positional occlusion or narrowing of subclavian artery with arm hyperabduction, external rotation
TOP DIFFERENTIAL DIAGNOSES
• Primary and secondary plexus tumors
• Radiation plexopathy
• Trauma
PATHOLOGY
• Cervical ribs, abnormal transverse processes, fibrous bands, scalene compression of thoracic outlet contents
CLINICAL ISSUES
• "True" neurological thoracic outlet syndrome: Intermittent arm pain, numbness, and weakness with hyperabduction, external rotation ○ Pain in shoulder, proximal upper extremity → neck ○ Paresthesias, numbness in forearm/hand
• Vascular thoracic outlet syndrome: Paresthesias 2° to arterial or venous ischemia ○ Obliteration of brachial, radial pulses with arm
hyperabduction and elevation
DIAGNOSTIC CHECKLIST
• Subclavian artery aneurysm, subclavian vein thrombosis, or brachial plexus compression at thoracic outlet strongly suggest thoracic outlet syndrome
(Left) Coronal graphic of the thoracic outlet demonstrates brachial plexus compression + a subclavian artery aneurysm st arising secondary to the C7 cervical rib ﬇ and anterior scalene muscle ſt compression. (Right) Anteroposterior radiograph demonstrates bilateral rudimentary C7 cervical ribs ﬇. The right cervical rib articulates with the 1st thoracic rib.
(Left) Sagittal oblique STIR MR shows normal anatomy of the interscalene triangle: Brachial plexus trunks , anterior ſt and middle scalene muscles, subclavian artery st, subclavian vein ﬈, and 1st thoracic rib ﬇. (The anterior is to the left per radiologic convention.) (Right) Sagittal oblique STIR MR (in a professional drummer) through the thoracic outlet shows mild T2 hyperintensity of some fascicles within the lower trunk , correlating with the clinical presentation with lower brachial plexopathy.
419