Isolated cervical juvenile xanthogranuloma in childhood

Citation
Pm. Rampini et al., Isolated cervical juvenile xanthogranuloma in childhood, SPINE, 26(12), 2001, pp. 1392-1395
Citations number
8
Categorie Soggetti
Neurology
Journal title
SPINE
ISSN journal
03622436 → ACNP
Volume
26
Issue
12
Year of publication
2001
Pages
1392 - 1395
Database
ISI
SICI code
0362-2436(20010615)26:12<1392:ICJXIC>2.0.ZU;2-V
Abstract
Study Design. This is a report of an exceptional case of isolated cervical juvenile xanthogranuloma in a child. Objectives. This case report draws attention to the fact that isolated xant hogranuloma of the central nervous system should be considered among possib le diagnosis of subdural extramedullary spinal masses in children and young adults. Summary and Background Data. Isolated juvenile xanthogranuloma of the centr al nervous system is extremely rare. When located in the spinal canal it be haves like any extramedullary mass-occupying lesion. MRI depicts the tumor' s association with adjacent structures. In cases in which a subtotal surgic al removal was possible, radiotherapy has been indicated. Methods. A three-year-old girl presented severe pain in the right shoulder and spastic tetraparesis. The MRI showed an intradural extramedullary mass homogeneously enhancing after DTPA-gadolinium infusion. Complete surgical r emoval of the tumor was performed through open-door laminoplasty. Results. The child was pain free immediately after the surgical removal of the tumor. A gradual complete recovery of the neurologic deficits followed. Open-door laminoplasty provided sufficient operative space, and it minimiz ed the impact on the growing spinal column. Conclusions. Isolated juvenile xanthogranuloma does not show any predilecti ons of localization inside the central nervous system. Both intracranial an d spinal juvenile xanthogranulomas appear isointense in MRI and enhance hom ogeneously with gadolinium. Whenever possible, total surgical removal alone seems to be curative. Otherwise, a subtotal removal of the tumor might be followed by radiotherapy. Immunohistochemical tests ensure the diagnosis.