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1.
Brain ; 122 ( Pt 7): 1383-90, 1999 Jul.
Article in English | MEDLINE | ID: mdl-10388803

ABSTRACT

MRI was performed on the spinal roots, brachial and lumbar plexuses of 14 patients with chronic inflammatory demyelinating polyneuropathy (CIDP). Hypertrophy of cervical roots and brachial plexus was demonstrated in eight cases, six of whom also had hypertrophy of the lumbar plexus. Of 11 patients who received gadolinium, five of six cases with hypertrophy and one of five without hypertrophy demonstrated enhancement. All patients with hypertrophy had a relapsing-remitting course and a significantly longer disease duration. Gross onion-bulb formations were seen in a biopsy of nerve from the brachial plexus in one case with clinically evident nodular hypertrophy. We conclude that spinal root and plexus hypertrophy may be seen on MRI, particularly in cases of CIDP of long duration, and gadolinium enhancement may be present in active disease.


Subject(s)
Brachial Plexus/pathology , Demyelinating Diseases/diagnosis , Lumbosacral Plexus/pathology , Magnetic Resonance Imaging , Peripheral Nervous System Diseases/diagnosis , Spinal Nerve Roots/pathology , Adult , Aged , Chronic Disease , Female , Humans , Male , Middle Aged , Radiography, Thoracic
2.
AJNR Am J Neuroradiol ; 16(4 Suppl): 952-4, 1995 Apr.
Article in English | MEDLINE | ID: mdl-7611083

ABSTRACT

Vertebral artery dissection after neck manipulation has been well described. A case of bilateral vertebral artery dissection diagnosed with dynamic CT scanning of the neck is reported. The CT appearances and correlative angiographic and MR findings are presented.


Subject(s)
Aortic Dissection/diagnostic imaging , Intracranial Aneurysm/diagnostic imaging , Tomography, X-Ray Computed , Vertebral Artery/diagnostic imaging , Adult , Aortic Dissection/etiology , Cerebral Angiography , Cervical Vertebrae , Chiropractic , Female , Humans , Intracranial Aneurysm/etiology
3.
Pediatr Radiol ; 23(3): 189-94, 1993.
Article in English | MEDLINE | ID: mdl-8332406

ABSTRACT

Infantile myofibromatosis is an unusual condition generally presenting in the newborn period. It may be solitary or multicentric. Sites involved include skin and subcutaneous tissues, muscle, bones and viscera. Nine cases are presented, including one case in an identical twin whose co-twin remained asymptomatic. The radiological features and differential diagnosis are discussed.


Subject(s)
Bone Neoplasms/diagnostic imaging , Leiomyoma/diagnostic imaging , Soft Tissue Neoplasms/diagnostic imaging , Bone Neoplasms/epidemiology , Diagnosis, Differential , Diseases in Twins , Female , Humans , Infant, Newborn , Leiomyoma/epidemiology , Male , Radiography , Soft Tissue Neoplasms/epidemiology
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