The coexistence of peripheral nerve sheath tumors and vitiligo: more than coincidence?

Mohamed A. Elsherif, Robert J. Spinner, Rachel Y. Miest

Research output: Contribution to journalArticlepeer-review

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 languageEnglish (US)
Pages (from-to)95-99
Number of pages5
JournalActa Neurochirurgica
Volume158
Issue number1
DOIs
StatePublished - 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

Fingerprint Dive into the research topics of 'The coexistence of peripheral nerve sheath tumors and vitiligo: more than coincidence?'. Together they form a unique fingerprint.

Cite this