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American Journal of Roentgenology, Vol 148, Issue 2, 381-391
Copyright © 1987 by American Roentgen Ray Society


Articles

The MR appearance of syringomyelia: new observations

JL Sherman, AJ Barkovich, and CM Citrin

Fifty-eight patients with spinal cord cavities were studied with MR imaging. Patients were separated into four groups, and the appearance of the cavities were compared. There were 24 patients (41.4%) with communicating syringomyelia (associated with the Chiari I malformation). Sixteen patients (27.6%) had posttraumatic syringomyelia, nine patients (15.5%) had associated tumors, and nine patients (15.5%) had idiopathic syringomyelia. The characteristics of each syrinx, the spinal cord, and the appearance of the cerebellar tonsils were analyzed on T2- and T1-weighted images. There is a striking similarity in the appearance of many syrinx cavities regardless of the cause. Characteristics that were found in some patients in every group included areas of increased intensity on T2-weighted images, the presence of the CSF flow-void sign (CFVS) in the syrinx cavity, eccentric cavities, "beaded" cavities, and cord enlargement. Tonsillar ectopia alone does not indicate that a syrinx is of the "communicating" type, since it was present in two of 16 patients (13%) with trauma and in two of five patients (40%) with tumors. T1-weighted images were most useful in evaluating the anatomic characteristics of the syrinx and the cerebellar tonsils. Most syrinx cavities involved the cervicothoracic junction. The average length was between five and nine vertebral segments (depending on category) but varied between one and 20 vertebral segments. T2-weighted images revealed areas of increased intensity in the spinal cord in 13 patients without tumors. Two of these cases were shown to represent gliosis on histopathologic review. The CFVS was present in the syrinx cavities of 23 patients (40%), probably reflecting pulsatile movements of the syrinx fluid. It has been proposed that such movements are a cause of syrinx propagation, and the observation of the CFVS may have prognostic significance. The development and progression of the CFVS was documented in serial MR examinations in one patient over an 18-month period. The theories of syrinx development and propagation are reviewed.
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A. Kastrup, T. Nagele, and H. Topka
Spontaneous resolution of idiopathic syringomyelia
Neurology, October 23, 2001; 57(8): 1519 - 1521.
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