eMedicine Specialties > Orthopedic Surgery > Pediatrics
Neurofibromatosis: Workup
Updated: Jan 15, 2009
Workup
Imaging Studies
- All patients with NF1 who undergo surgery, who require endotracheal anesthesia, who undergo halo traction, or who present with neck tumors should undergo cervical radiographic series. If subluxation is suspected, tomograms, CT scans, and/or MRIs are appropriate. Other reasons for obtaining cervical spinal radiographs in a patient with NF1 include the evaluation of torticollis and dysphagia.
- After the posterior excision of a neck mass, progressive cervical kyphosis is possible. If any suspicious area is noted on plain radiographs, right and left oblique views should be obtained to look for widening of the neuroforamina. These may represent dumbbell lesions (ie, widening of the neuroforamina caused by the exit of a neurofibroma from the spinal canal).
- High-volume myelography or MRI should be used in the investigation of all dystrophic curves prior to treatment.
- Lateral thoracolumbosacral spinal radiographs should be closely scrutinized for thoracic lordosis and cervicothoracic kyphosis.
- MRI should be performed to evaluate any spinal deformity in NF1. Surgery would be performed only in situ, noninstrumented without MRI.
Other Tests
- All preadolescent children with neurofibromatosis should be evaluated with scoliosis screening, or the bend test, to exclude a spinal deformity.
More on Neurofibromatosis |
| Overview: Neurofibromatosis |
Workup: Neurofibromatosis |
| Treatment: Neurofibromatosis |
| Follow-up: Neurofibromatosis |
| References |
| Further Reading |
| « Previous Page | Next Page » |
References
Crawford AH. Neurofibromatosis. In: Stuart L, Weinstein R, eds The Pediatric Spine, Principles and Practice. Vol 1. 1994.
Duymaz A, Karabekmez FE, Keskin M, Tosun Z. Neurofibromatosis in a family: is there a tendency to one side of the face?. J Plast Reconstr Aesthet Surg. Oct 2008;61(10):1169. [Medline].
Cheng SF, Chen YI, Chang CY, Peng Y, Liao SL. Malignant peripheral nerve sheath tumor of the orbit: malignant transformation from neurofibroma without neurofibromatosis. Ophthal Plast Reconstr Surg. Sep-Oct 2008;24(5):413-5. [Medline].
Tibbles JA, Cohen MM Jr. The Proteus syndrome: the Elephant Man diagnosed. Br Med J (Clin Res Ed). Sep 13 1986;293(6548):683-5. [Medline].
Crawford AH, Schorry EK. Neurofibromatosis in children: the role of the orthopaedist. J Am Acad Orthop Surg. Jul-Aug 1999;7(4):217-30. [Medline].
Crawford AH. Neurofibromatosis in childhood. Instr Course Lect. 1981;30:56-74. [Medline].
Crawford AH. Neurofibromatosis in children. Acta Orthop Scand Suppl. 1986;218:1-60. [Medline].
Wozniak W, Karwacki MW. Is "watchful waiting" superior to surgery in children with neurofibromatosis type 1 presenting with extracranial and extramedullary tumor mass at diagnosis?. Childs Nerv Syst. Jul 1 2008;[Medline].
de Oliveira MG, Pozatti Moure S, Sérgio Batista P, Moraes Chaves AC, Rados PV, Sant Ana Filho M. NF1 diagnosis criteria and associated sarcomatous tumor review of the literature and case report. Oral Maxillofac Surg. Sep 25 2008;[Medline].
Cairns AG, North KN. Cerebrovascular dysplasia in neurofibromatosis type 1. J Neurol Neurosurg Psychiatry. Oct 2008;79(10):1165-70. [Medline].
Yong-Hing K, Kalamchi A, MacEwen GD. Cervical spine abnormalities in neurofibromatosis. J Bone Joint Surg Br. 1969;51:843-7.
Curtis BH, Fisher RL, Butterfield WL, Saunders FP. Neurofibromatosis with paraplegia. Report of eight cases. J Bone Joint Surg Am. Jul 1969;51(5):843-61. [Medline].
Hsu LC, Lee PC, Leong JC. Dystrophic spinal deformities in neurofibromatosis. Treatment by anterior and posterior fusion. J Bone Joint Surg Br. Aug 1984;66(4):495-9. [Medline].
Sirois JL 3rd, Drennan JC. Dystrophic spinal deformity in neurofibromatosis. J Pediatr Orthop. Jul-Aug 1990;10(4):522-6. [Medline].
Li M, Fang X, Li Y, Ni J, Gu S, Zhu X. Successful use of posterior instrumented spinal fusion alone for scoliosis in 19 patients with neurofibromatosis type-1 followed up for at least 25 months. Arch Orthop Trauma Surg. Jul 24 2008;[Medline].
Taylor T, Jaspan T, Milano G, Gregson R, Parker T, Ritzmann T, et al. Radiological classification of optic pathway gliomas: experience of a modified functional classification system. Br J Radiol. Oct 2008;81(970):761-6. [Medline].
Carroll SL, Ratner N. How does the Schwann cell lineage form tumors in NF1?. Glia. Sep 19 2008;56(14):1590-1605. [Medline].
Crawford AH. Management of skeletal complications. In: Von Recklinghausen's Neurofibromatosis. Vol 6. NIH Consensus Development Conference Statement;1987.
Further Reading
Neurofibromatosis type 1 in genetic counseling practice: recommendations of the National Society of Genetic Counselors.
National Society of Genetic Counselors. 2007 Aug. 21 pages. NGC:006248
Long-term follow-up guidelines for survivors of childhood, adolescent, and young adult cancers. Sections 38-91: radiation. Children's Oncology Group. 2003 Sep (revised 2006 Mar). 74 pages. NGC:005599
Related eMedicine topics:
Neurofibromatosis, Type 1 (Neurology)
Neurofibromatosis, Type 2 (Neurology)
Neurofibromatosis Type 1 (Radiology)
Neurofibromatosis Type 2 (Radiology)
Keywords
neurofibromatosis, von Recklinghausen's disease, von Recklinghausen disease, neurofibromatosis type 1, NF1, peripheral neurofibromatosis, neurofibromatosis type 2, NF2, central neurofibromatosis
Workup: Neurofibromatosis