Meningeal hemangiopericytoma
Meningeal hemangiopericytoma
Meningeal hemangiopericytoma
Meningeal hemangiopericytoma
Meningeal hemangiopericytoma
Meningeal hemangiopericytoma
Solitary fibrous tumors of the dura
Solitary fibrous tumors of the dura
Solitary fibrous tumors of the dura
Solitary fibrous tumors of the dura
Solitary fibrous tumors of the dura
Solitary fibrous tumors of the dura
Solitary fibrous tumors of the dura
Solitary fibrous tumors of the dura
Solitary fibrous tumors of the dura are histologically identical to hemangiopericytomas, which are now classified as WHO grade 2-3 SFTs rather than separate entities (2016 WHO classification)
Clinical presentation is nonspecific and identical to other dural masses, with headache being the most common symptom
Complete surgical resection is usually curative, but recurrence rates are highly variable (reported up to 50%), with incomplete resection or recurrence requiring adjuvant radiotherapy
Rare paraneoplastic syndromes include non-islet cell tumor hypoglycemia (NICTH) from IGF-2 secretion and acromegaly
The key imaging distinguishing feature is low T2 signal intensity, which is much less common in the more frequent meningioma
Unlike meningiomas, SFTs of the dura are often larger, more vividly enhancing, have prominent surface flow voids, and lack intralesional calcification
Describe the mass as an extra-axial dural lesion with intermediate T1 signal, low-to-isointense T2 signal (specifically noting 'yin-yang' heterogeneity if present), vivid heterogeneous enhancement with prominent surface flow voids, and lack of intralesional calcification; emphasize that while appearance overlaps with meningioma (which should remain the primary diagnosis given frequency), the combination of low T2 signal and prominent enhancement without calcification favors solitary fibrous tumor.