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Abnormal pigmentation of schwannoma attributed to excess production of neuromelanin‐like pigment
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AbstractFive cases of non‐melanotic pigmented schwannoma with excess accumulation of neuromelanin are presented. The tumors were composed basically of spindle or fusiform tumor cells, compatible with those of classical schwannoma, together with varying numbers of tumor cells containing various amounts of light brown or grayish pigment. Fontana‐Masson stain demonstrated argentaffin granules in some tumor cells of each tumor and bleaching with potassium permanganate abolished argentaffin reaction. Ultrastructural examination demonstrated the granules contained fine particles with heterogeneous density, occasionally together with coarse granular materials or amorphous high‐density areas, indicating lysosome or autophagosome. Neither typical melanosomes nor neurosecretory granules were detected. In immunohistochemistry, neurogenic markers as well as CD68 were expressed in most tumor cells in each case and various numbers of tumor cells were positive for Leu7 and CD34. Lysozyme was also frequently positive in tumor cells, especially in granular cells. HMB45 was not expressed in any of the cases. These findings indicate that these cases are schwannomas with abnormal accumulation of neuromelanin‐like pigment.
Title: Abnormal pigmentation of schwannoma attributed to excess production of neuromelanin‐like pigment
Description:
AbstractFive cases of non‐melanotic pigmented schwannoma with excess accumulation of neuromelanin are presented.
The tumors were composed basically of spindle or fusiform tumor cells, compatible with those of classical schwannoma, together with varying numbers of tumor cells containing various amounts of light brown or grayish pigment.
Fontana‐Masson stain demonstrated argentaffin granules in some tumor cells of each tumor and bleaching with potassium permanganate abolished argentaffin reaction.
Ultrastructural examination demonstrated the granules contained fine particles with heterogeneous density, occasionally together with coarse granular materials or amorphous high‐density areas, indicating lysosome or autophagosome.
Neither typical melanosomes nor neurosecretory granules were detected.
In immunohistochemistry, neurogenic markers as well as CD68 were expressed in most tumor cells in each case and various numbers of tumor cells were positive for Leu7 and CD34.
Lysozyme was also frequently positive in tumor cells, especially in granular cells.
HMB45 was not expressed in any of the cases.
These findings indicate that these cases are schwannomas with abnormal accumulation of neuromelanin‐like pigment.
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