| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3095081 | World Neurosurgery | 2015 | 5 Pages |
Abstract
The diagnosis of OIT should be considered in a case of severe hypophosphatemia and metabolic bone disease that is not explained by any other metabolic or hereditary disease. These tumors can occur intracranially and may be confused with a meningioma or a hemangiopericytoma. Taking OIT into consideration in such cases could lead to a shorter time to diagnosis and management, which in our case took 4 years.
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Neuroscience
Neurology
Authors
Hussein Fathalla, Michael Cusimano, Antonio Di Ieva, Jason Karamchandani, Raymond Fung, Kalman Kovacs,