Schwannian and Perineuriomatous Differentiation in a Series of Giant Congenital Melanocytic Nevi.
Irina KletskayaIrena BelousovaOlga MakarovaAnton NarbutovRaisa OganesyanMichele DonatiJan ŘíčařClaudia M SalgadoMiguel Reyes-MúgicaDmitry V KazakovPublished in: The American Journal of dermatopathology (2024)
Close relationship between melanocytes and neural cells is accepted to reflect their common derivation from the neural crest and tumors combining both elements. We present a series of 10 patients with giant congenital melanocytic nevi (CMN) in which a secondary proliferation (11 lesions) with schwannian and/or perineuriomatous differentiation developed in the course of the disease. The age of the patients (4 male and 6 female) at the time of surgery and histological assessment varied from 3 months to 57 years. Histopathologically, the following subgroups were delineated: (1) nodular/tumoriform "neurotization" in CMN, (2) diffuse neurofibroma-like proliferation within CMN, (3) plexiform neurofibroma-like proliferation within CMN, and (4) diffuse perineuriomatous (hybrid schwannomatous-perineuriomatous) differentiation in CMN. We review the pertinent literature, including the role of recently identified Schwann cell precursors which are believed to represent the nerve-associated state of neural crest-like cells that persists into later developmental stages.
Keyphrases
- signaling pathway
- end stage renal disease
- induced apoptosis
- ejection fraction
- chronic kidney disease
- systematic review
- minimally invasive
- newly diagnosed
- low grade
- prognostic factors
- peripheral nerve
- single cell
- peritoneal dialysis
- cell cycle arrest
- cell therapy
- acute coronary syndrome
- oxidative stress
- endoplasmic reticulum stress
- cell death
- cell proliferation
- bone marrow
- patient reported outcomes