Coexpression of Neurofilament and Keratin Proteins in Cutaneous Neuroendocrince Carcinoma Cells

Four cases of neuroendocrine carcinomas (NECA) of the skin were studied by indirect immunofluorescence, using a monoclonal antikeratin antibody and a polyclonal antineurofilament antibody. Fifty to ninety percent and 80 to >95% of the NECA cells stained with the antineurofilament antibody and the...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of investigative dermatology 1986-01, Vol.86 (1), p.74-77
Hauptverfasser: Merot, Yves, Margolis, Randall J., Dahl, Doris, Saurat, Jean-H, Mihm, Martin C
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Four cases of neuroendocrine carcinomas (NECA) of the skin were studied by indirect immunofluorescence, using a monoclonal antikeratin antibody and a polyclonal antineurofilament antibody. Fifty to ninety percent and 80 to >95% of the NECA cells stained with the antineurofilament antibody and the antikeratin antibody, respectively. Using double-labeling indirect immunofluorescence could also demonstrate that, in 3 cases studied, some of the NECA cells, but not all, stained with both antikeratin and antineurofilament antibodies. These results, together with the recent knowledge of the intermediate filament protein type of normal Merkel cells (MC), tend to support the hypothesis that NECA cells do not originate from epithelial MC but from dermal neuroendocrine cells. A dual concept of intraepithelial MC and extraepithelial intradermal neuroendocrine cells, “from possible distinct origin,” is proposed. Such a system has already been suggested for the neuroendocrinc cells of the appendix and bronchial mucosae.
ISSN:0022-202X
1523-1747
DOI:10.1111/1523-1747.ep12283862