Neurofibroma diagnostic criteria: Difference between revisions
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==Diagnostic criteria== | ==Diagnostic criteria== | ||
Following is the '''general diagnostic criteria''' for neurofibroma: | |||
* Randomly oriented thin spindled cells with wavy, hyperchromatic nuclei | * Randomly oriented thin spindled cells with wavy, hyperchromatic nuclei | ||
** Cellularity and organization are generally insufficient to produce palisading | ** Cellularity and organization are generally insufficient to produce palisading | ||
Latest revision as of 17:46, 29 March 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sara Mohsin, M.D.[2]
Overview
Diagnostic criteria
Following is the general diagnostic criteria for neurofibroma:
- Randomly oriented thin spindled cells with wavy, hyperchromatic nuclei
- Cellularity and organization are generally insufficient to produce palisading
- Thin processes with indistinct cytoplasm
- Most nuclei are small and bland
- Generally hypocellular
- Thin and thick collagen strands (“shredded carrot collagen”)
- Variable myxoid material surrounding cells and collagen
- Occasional mast cells and lymphocytes, rare foam cells
- Diffusely S100 immunoreactive
- Entrapped axons of overrun nerve frequently scattered within lesion
- Nerve frequently not grossly identifiable
- May show localized hyperchromatic atypical cells (“ancient change”)
- Localized cells with large, pleomorphic nuclei, cytoplasmic intranuclear inclusions, smudgy chromatin, and inconspicuous nucleoli
- Often large, long standing lesions
- Low mitotic index