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Primary intracranial aggressive fibromatosis arising in sella turcica: illustrative case

Kenta Ujifuku, Eisakua Sadakata, Shiro Baba, Koichi Yoshida, Kensaku Kamada, Minoru Morikawa, Kuniko Abe, Kazuhiko Suyama, Yoichi Nakazato, Isao Shimokawa, and Takayuki Matsuo

ICA. Coil embolization was additionally performed (data not shown). At the first pathological examination, an inflammatory myofibroblastic tumor (allergic granulomatosis) was suspected, and steroid pulse therapy was introduced but was ineffective. After a few months, the patient complained of headache, impaired left visual acuity, painful ophthalmoplegia, trigeminal neuralgia, diabetes insipidus, and panhypopituitarism. MRI revealed the tumor recurrence, with the lesion now gradually enhanced with gadolinium on T1WI ( Fig. 1H and I ). Hormone replacement therapy

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Long-term survival in patients with long-segment complex meningiomas occluding the dural venous sinuses: illustrative cases

Zhishuo Wei, Arka N. Mallela, Andrew Faramand, Ajay Niranjan, and L. Dade Lunsford

trigeminal neuralgia (TGN) 24 months after her craniotomy and was treated with SRS for management of her facial pain. She underwent repeat SRS 120 months after the initial craniotomy for recurrent tumor. Repeat trigeminal GK SRS was performed three times for recurrent pain. At 243 months after the initial craniotomy, her tumor and facial pain were stable. B: The radiosurgery dose plan projected on the axial, coronal, and sagittal views for stages 1, 2, and 3 of the first and second SRS. The 214-month follow-up MRI after first GK shows stable tumor. Images obtained 2