Publication | Open Access
A Rare Case of Neurofibromatosis Recklinghausen (Plexiform Type)
496
Citations
6
References
1956
Year
MedicineNeurofibromatosis RecklinghausenSurgical PathologyHistopathologyMultiple NeurofibromatosisOral CavityUnusual LocalizationNeuropathologyNeuromasDiagnostic NeuroradiologyPathologic LesionConnective Tissue Disease
Neurofibromatosis type 1 is usually diagnosed clinically, but atypical localization—especially in the head, neck, and oral cavity—can make diagnosis difficult, underscoring the need for dental awareness of its oral manifestations. This paper presents a case of neurofibromatosis type 1 with unusual head, neck, and oral cavity involvement.
AbstractTypical cases of multiple neurofibromatosis of Recklinghausen are easy to diagnose from a clinical point of view. The mono-symptomatic cases can also be easily diagnosed i f they occur in patients with hereditary backgrounds. However, unusual localization in both types may render the diagnosis difficult. The case to be described in this paper is an example of unusual localization in the head, neck, and oral cavity. From the view point of differential diagnosis, the dentist should be familiar with the disease in its oral manifestation.
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