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Erschienen in: Orphanet Journal of Rare Diseases 1/2013

Open Access 01.12.2013 | Research

The molecular mechanisms on glomangiopericytoma invasion

verfasst von: Qiang Sun, Chunye Zhang, Wantao Chen, Yue He

Erschienen in: Orphanet Journal of Rare Diseases | Ausgabe 1/2013

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Abstract

Purpose

To observed the imaging and pathological features of the glomangiopericytoma.

Experimental design

In this paper we report a typical case of glomangiopericytoma arising in the skull base area and summarize the clinical manifestations, imaging and pathological features of such diseases.

Results

Immunohistochemical staining confirmed the tumor cells were strongly positive to Vim, SMA, MSA and negative to CD31, CD34. Partial cells were positive to FVIII. The imaging can’t confirm the diagnosis but indicate the the tumor has intact envelope.The cells in the tumor envelope is positive to Vim and negative SMA and FVIII. These findings were compatible with glomangiopericytoma and the cells in the tumor envelope is not glomangiopericytoma cells.

Conclusion

In view of the clinical and pathological features of the glomangiopericytoma, we believe that the surgery is the best treatment so far and the tumor can be resected completely. The above results can be preliminary reason to explain the low recurrence of such diseases.
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Metadaten
Titel
The molecular mechanisms on glomangiopericytoma invasion
verfasst von
Qiang Sun
Chunye Zhang
Wantao Chen
Yue He
Publikationsdatum
01.12.2013
Verlag
BioMed Central
Erschienen in
Orphanet Journal of Rare Diseases / Ausgabe 1/2013
Elektronische ISSN: 1750-1172
DOI
https://doi.org/10.1186/1750-1172-8-152

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