| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6045463 | World Neurosurgery | 2015 | 25 Pages |
Abstract
Xanthogranuloma, although extremely rare in the pediatric population, may present as a calcified suprasellar mass and manifest with primary amenorrhea. The prognosis after gross total resection is likely favorable; however, long-term follow-up is indicated for these rare neoplasms.
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Neurology
Authors
Atef Ben Nsir, Quoc-Anh Thai, Larbi Chaieb, Hafedh Jemel,