Cerebral amyloidoma
https://doi.org/10.63769/1683-3295-2025-27-3-125-133
Abstract
Amyloidoma is a non-tumor lesion characterized by local deposits of insoluble protein aggregates of κ/λ immunoglobulin light chains in tissues. This condition is also known as AL-amyloidosis and it is not associated with systemic amyloidosis. The usage of term “amyloidoma” is due to the fact that this lesion acts like a tumor according to clinical and neurovisualization signs but it is not a tumor.
The correct diagnosis is difficult due to small number of described cases as well as absence of specific clinical symptoms and tumor-like natural history. The most reliable diagnostic method is histological examination. We present 2 clinical cases of cerebral amyloidoma, confirmed histologically.
About the Authors
I. V. GrigorievRussian Federation
Ilya V. Grigoriev.
Bld. 10, 1 Ostrovityanova St., Moscow 117513
K. S. Esina
Russian Federation
18 Bulanova St., Toksovo Village, Leningrad Region 188664
O. O. Kordonskaya
Russian Federation
Bld. 10, 1 Ostrovityanova St., Moscow 117513
S. A. Mamykina
Russian Federation
Bld. 10, 1 Ostrovityanova St., Moscow 117513
O. I. Patsap
Russian Federation
Bld. 10, 1 Ostrovityanova St., Moscow 117513
S. A. Melchenko
Russian Federation
Bld. 10, 1 Ostrovityanova St., Moscow 117513
I. V. Senko
Russian Federation
Bld. 10, 1 Ostrovityanova St., Moscow 117513
M. B. Dolgushin
Russian Federation
Bld. 10, 1 Ostrovityanova St., Moscow 117513
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Review
For citations:
Grigoriev I.V., Esina K.S., Kordonskaya O.O., Mamykina S.A., Patsap O.I., Melchenko S.A., Senko I.V., Dolgushin M.B. Cerebral amyloidoma. Russian journal of neurosurgery. 2025;27(3):125-133. https://doi.org/10.63769/1683-3295-2025-27-3-125-133

























