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[Local immune response in neurofibromatosis type 1 and type 2]
P L Gerosa1, C Vai, L Bizzozero
1Reparto Ortopedia e Traumatologia II, Ospedale Niguarda, Milano.
Minerva Medica
|February 1, 1993
Abstract:
Neurofibromatosis, in all its variant forms, is a hereditary disease characterized by dysplasia, neoplasia, and the tendency to expand and undergo malignant transformation. We underline the presence of chronic inflammation and of immunologic interdependency. The immune reactions against the non-self have been investigated histologically in light of the concepts of immunosurveillance and immunotolerance. Such investigations would ameliorate subsequent studies and favour the employment of immunomodulatory treatments.