Neurofibromatoses are genetic disorders of the nervous system.Mainly, these disorders affect the growth and development of nerve cell tissue. The disorders are known as neurofibromatosis type 1.
A neurofibroma is a benign nerve-sheath tumor in the peripheral nervous system.In 90% of cases, they are found as stand-alone tumors, while the remainder are found in persons with neurofibromatosis type I (NF1), an autosomal-dominant genetically inherited disease, they can result in a range of symptoms from physical disfiguration and pain to cognitive disability.Specialty: Oncology.
About our Center. UCLA Multidisciplinary NF Clinic. The UCLA NF2 Clinic offers a comprehensive multidisciplinary approach for neurofibromatosis type 2 (NF2) and schwannomatosis patients. The core team includes pediatric and adults neuro-oncologists, neurosurgeons, neuro .
The term fibromatosis refers to a group of soft tissue tumors which have certain characteristics in common, including absence of cytologic and clinical malignant features, a histology consistent with proliferation of well-differentiated fibroblasts, an infiltrative growth pattern, and aggressive clinical behavior with frequent local recurrence.It is classed by the World Health Organisation as Specialty: Oncology.
Neurofibroma: Introduction. Neurofibroma: A benign tumor that originates from nerve cells. The tumors usually arise from nerves in the skin or just under the skin. More detailed information about the symptoms, causes, and treatments of Neurofibroma is available below.. Symptoms of NeurofibromaNext: Symptoms of Neurofibroma.