Abstract
Neurocristopathies arise from abnormal migration, differentiation, or proliferation of neural crest derivatives, leading to diverse clinical and pathological features. They are classified into dysgenetic or neoplastic, and can affect single or multiple sites (simple versus complex). Examples include congenital melanocytic nevi, neuroblastoma, Hirshsprung’s disease, Waardenburg’s syndrome, neurofibromatosis (NF) 1 and multiple endocrine neoplasia (MEN) 2A and 2B. We report two cases of peripheral nerve sheath tumors associated with vitiligo and discuss the possible implicated embryologic, genetic and molecular mechanisms. To our knowledge, we also report the first case of de novo malignant peripheral nerve sheath tumor (MPNST) associated with vitiligo.
Original language | English (US) |
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Pages (from-to) | 95-99 |
Number of pages | 5 |
Journal | Acta Neurochirurgica |
Volume | 158 |
Issue number | 1 |
DOIs | |
State | Published - Jan 1 2016 |
Keywords
- Malignant peripheral nerve sheath tumors
- Neurocristopathies
- Peripheral nerve sheath tumors
- Schwannoma
- Vitiligo
ASJC Scopus subject areas
- Surgery
- Medicine(all)
- Clinical Neurology