Neurofibromatosis is a condition characterized by multiple growths which derive from primitive cells in the body. The growths occur along nerve paths, anywhere in the body. Neurofibromatosis skin lesions are typically flat, pigmented patches but occasionally are elevated flesh-colored bumps [See figure 1].
Neurofibromatosis tends to run in families. Each child of an involved parent has a 50% chance of developing neurofibromatosis. In neurofibromatosis type I, chromosome 17 is responsible for the disease while chromosome 22 is responsible for neurofibromatosis type II. Nearly 50% of the cases have no family history of neurofibromatosis, so the cause is a new mutation.
Neurofibromatosis type I is more common than neurofibromatosis type II. About 1 in 3000-5000 has neurofibromatosis type I, while about 1 in 25,000 have type II.
Neurofibromatosis type I may affect family members differently. Some family members may have minimal disease, while others may be more severely affected. Some of the characteristic findings are:
• Skin findings: Freckles (cafe-au-lait spots) on the skin. These dark spots are typically greater than 5mm in diameter (often irregularly shaped) and are usually located under the arms, in the bend of the elbow and knee, and around the groin region. The spots tend to increase in size and number during the first 10 years of life. Nodule(s) on the skin may develop at any age [See figure 1].
• Eye findings: The eyelids may become thicker and irregularly shaped because of the growth of a neurofibroma [See figure 2]. Children with this eyelid problem are at risk for developing high eye pressure (glaucoma).
• Pigmented spots on the iris may increase in number over time. These spots are called Lisch nodules and do not affect vision [See figure 3].
• Lesions may occur in the inner layers of the eye (choroid), but do not affect vision.
• The nerve which connects the eye to the brain is the optic nerve. The optic nerve can develop a benign tumor called a glioma [See figure 4]. This tumor may cause vision problems.
• Bone findings: A child with neurofibromatosis may have poor development of arm and leg bones. Also, a bone around the eye (sphenoid) may be poorly developed or absent which can cause the eye to pulsate.
• Other less commonly associated findings: crooked spine (scoliosis), seizures, decreased intellect, large head, malignancy (leukemia, Wilm's tumor, rhabdomyosarcoma, and pheochromocytoma).
Type II typically presents in the teens or early adulthood with hearing problems due to the development of an ear nerve tumor (acoustic neuroma). Other findings include: problems with balance, early cataract (posterior subcapsular cataract, wedge cortical cataracts), spots on the iris (Lisch nodules), or other nervous system tumors.
If an eyelid with neurofibroma becomes ptotic and/or excessively large, surgical debulking may be necessary. Surgery for residual ptosis may be required. Unfortunately, the eyelid lesion may recur. Frequently, optic nerve gliomas simply require observation by serial examinations and no intervention is required. Lesions confined to the optic nerve occasionally require excision. If a glioma extends to the brain, increased fluid pressure around the brain (hydrocephalus) or pituitary problems may occur. Brain involvement may require treatment with chemotherapy and/or radiation.
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