neurofibromatosis
Neurofibromatoses (NF) comprise a number of clinically and genetically distinct inherited conditions that carry a high risk of tumor formation. They fall under the wider classification of phakomatoses. The tumors particularly involve the central and peripheral nervous systems:
Siehe auch:
und weiter:
- Proteus-Syndrom
- Beckwith-Wiedemann-Syndrom
- Kongenitale Tibiapseudarthrose
- Drusen der Papilla nervi optici
- multiple zystische Lungenherde
- Café-au-lait-Fleck
- conditions involving skin and bone
- abdominal aortic coarctation
- sporadisches Neurofibrom
- Hemihypertrophie
- thorakale Meningozele
- cutaneous neurofibromas
- intraspinales Schwannom
- gracile bones (mnemonic)
- mass involving the foramen of Monro or/and superior third ventricle
- Elephantiasis
- very bizarre generalised lesions (mnemonic)
- Hemihyperplasie
- thoracic meningocele in a patient with neurofibromatosis
- Neurofibromatose der Mamma
- intracranial findings in neurofibromatosis type 1
