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[Rosai-Dorfman intracranial histiocytosis: case report and literature review].

作者信息

Shevchenko K V, Shimansky V N, Zolotova S V, Galstyan S A, Tanyashin S V, Karnaukhov V V, Kugushev I O

机构信息

Burdenko Neurosurgical Center, Moscow, Russia.

出版信息

Zh Vopr Neirokhir Im N N Burdenko. 2022;86(1):81-90. doi: 10.17116/neiro20228601181.

DOI:10.17116/neiro20228601181
PMID:35170280
Abstract

Histiocytosis is a group of idiopathic diseases accompanied by metabolic disorders and accumulation of metabolic products in histiocytes. Isolated Rosai-Dorfman histiocytosis of central nervous system is observed in less than 5% of cases. The authors report treatment and follow-up of a patient with intracranial Rosai-Dorfman disease. There were symptoms of lesion of the left cerebellopontine angle and epileptic seizures. Preoperative MRI identified two tumors (posterior cranial fossa on the left and right-sided parasagittal neoplasm). The authors carried out total resection of supratentorial tumor, after 3 weeks - subtotal resection of tumor in posterior cranial fossa. No recurrence after total resection was observed. Irradiation of infratentorial tumor with a total focal dose of 50 Gy after 6 months resulted tumor shrinkage throughout 12 months. Radiotherapy with the same dose was repeated throughout subsequent 12-month follow-up period due to progression of this focus. This treatment had a positive effect, but new skull base foci occurred. The authors emphasize the effectiveness of total resection and lower efficiency of subtotal excision combined with radiotherapy.

摘要

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