Neurofibromatosis type 1 CT scan: Difference between revisions
Jump to navigation
Jump to search
MoisesRomo (talk | contribs) No edit summary |
MoisesRomo (talk | contribs) No edit summary |
||
| Line 5: | Line 5: | ||
==Overview== | ==Overview== | ||
There are no [[CT scan]] findings associated with [[neurofibromatosis type 1]], however, a [[Computed tomography|CT scan]] may be helpful in the [[diagnosis]] of complications. | There are no [[CT scan]] findings associated with [[neurofibromatosis type 1]], however, a [[Computed tomography|CT scan]] may be helpful in the [[diagnosis]] of complications. | ||
The use of routine [[Screening test|screening]] [[brain]] [[Computed tomography|CT scans]] in patients with [[neurofibromatosis type 1]] is controversial. | |||
The use of routine [[Screening test|screening]] [[brain]] [[Computed tomography|CT scans]] in patients with [[neurofibromatosis type 1]] is controversial. | |||
==CT scan== | ==CT scan== | ||
Latest revision as of 14:50, 1 September 2020
|
Neurofibromatosis type 1 Microchapters |
|
Differentiating Neurofibromatosis type 1 from other Diseases |
|---|
|
Diagnosis |
|
Treatment |
|
Case Studies |
|
Neurofibromatosis type 1 CT scan On the Web |
|
American Roentgen Ray Society Images of Neurofibromatosis type 1 CT scan |
|
Risk calculators and risk factors for Neurofibromatosis type 1 CT scan |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Moises Romo M.D.
Overview
There are no CT scan findings associated with neurofibromatosis type 1, however, a CT scan may be helpful in the diagnosis of complications. The use of routine screening brain CT scans in patients with neurofibromatosis type 1 is controversial.
CT scan
- There are no CT scan findings associated with neurofibromatosis type 1.[1] However, a CT scan may be helpful in the diagnosis of complications of neurofibromatosis type 1, which include:
- Optic pathway gliomas. Early detection may prevent vision loss and improve outcomes.[2]
- Intracranial mases[3]
- Chiari malformations[3]
- Pheochromocytomas[3][4]
- Benign hamartomas[3]
- Changes in ventricular size and hydrocephalus[3]
- The use of routine screening brain CT scans in patients with neurofibromatosis type 1 is controversial. Many physicians prefer to order a CT scan at the moment of the diagnosis and repeat later only if suspicious symptoms arise[3]
References
- ↑
- ↑ Listernick R, Louis DN, Packer RJ, Gutmann DH (February 1997). "Optic pathway gliomas in children with neurofibromatosis 1: consensus statement from the NF1 Optic Pathway Glioma Task Force". Ann. Neurol. 41 (2): 143–9. doi:10.1002/ana.410410204. PMID 9029062.
- ↑ 3.0 3.1 3.2 3.3 3.4 3.5
- ↑ Karagiannis A, Mikhailidis DP, Athyros VG, Harsoulis F (December 2007). "Pheochromocytoma: an update on genetics and management". Endocr. Relat. Cancer. 14 (4): 935–56. doi:10.1677/ERC-07-0142. PMID 18045948.