Glial FibriUary Acidic Protein (GFAP) Immunoreactivity in Peripheral Nerve Sheath Tumors
Autor: | Elizabeth F. Brown, Victor E. Gould, Vincent A. Memoli |
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Rok vydání: | 1984 |
Předmět: |
Pathology
medicine.medical_specialty Radioimmunoassay macromolecular substances Schwannoma Pathology and Forensic Medicine law.invention Peripheral Nervous System Neoplasms Structural Biology law Glial Fibrillary Acidic Protein medicine Humans Intermediate filament Cytoskeleton Neurofibroma Glial fibrillary acidic protein biology Chemistry medicine.disease GFAP stain nervous system Cytoplasm biology.protein Immunohistochemistry Electron microscope Neurilemmoma |
Zdroj: | Ultrastructural Pathology. 7:269-275 |
ISSN: | 1521-0758 0191-3123 |
DOI: | 10.3109/01913128409141487 |
Popis: | A spectrum of 24 benign and malignant nerve sheath tumors and 10 non-neural spindle-cell tumors were studied by light microscopy for the presence of glial fibrillary acidic protein (GFAP) immunoreactivity by the peroxidase-antiperoxidase (PAP) technique. In 8 cases, these results were compared to their electron microscopic appearances. Seventy percent (7 of 10) of benign schwannomas and 50% (4 of 8) of benign neurofibromas demonstrated focal to diffuse GFAP immunoreactivity. None of the malignant nerve sheath tumors nor any of the non-neural spindle-cell neoplasms contained demonstrable GFAP immunoreactivity. Similarly, no GFAP immunoreactivity could be detected in Schwann cells in normal peripheral nerves. The solitary benign schwannoma available for electron microscopic study demonstrated diffuse and abundant cytoplasmic intermediate filaments, and this tumor displayed diffuse and intense GFAP immunoreactivity. Two benign neurofibromas showed a more variable content of intermediate filaments ultrastructurally, and their GFAP immunoreactivity was variable. All five malignant nerve sheath tumors studied by electron microscopy displayed a variable complement of intermediate filaments; however, none of these tumors possessed GFAP immunoreactivity, suggesting that these intermediate filaments are either members of a different class of intermediate filaments or may perhaps represent "altered" GFAP not recognized by these antisera. |
Databáze: | OpenAIRE |
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