Tumor fibroso solitario/hemangiopericitoma de la médula espinal.

Citation data:

Neurocirugia (Asturias, Spain), ISSN: 2340-6305, Vol: 29, Issue: 6, Page: 309-313

Publication Year:
2018
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PMID:
29559217
DOI:
10.1016/j.neucir.2018.01.005
Author(s):
Flores-Justa, Ana; López-García, Elena; García-Allut, Alfredo; Reyes-Santías, Rosa María
Publisher(s):
Elsevier BV
Tags:
Medicine
article description
Solitary fibrous tumours/haemangiopericytomas (SFT/HPC) are fibroblastic mesenchymal neoplasms that harbour a genetic fusion of NAB2/STAT6. There are few reported cases in the central nervous system (CNS), of which spinal tumours are minority. We present a case of a 63-year-old woman with progressive paraparesis and a sensory level of T6. On the MRI we detected an intradural extramedullary lesion on T9-T10. We performed a laminectomy with an intraoperative ultrasound study in which we observed a heterogeneous lesion with an infiltrating pattern affecting the medulla at several points, and resection of the lesion. Immunohistological findings revealed positivity for vimentin, CD34 and STAT6; Ki-67 was 2%. A final diagnosis of SFT/HPC with SFT phenotype was made. SFT/HPC of the CNS is a rare neoplasm that should be taken into account in the differential diagnosis of these kinds of lesions, as clinical and MRI findings often lead to errors in diagnostic approach. The support of intraoperative ultrasound can assist in surgical decision-making.