Cervical myelopathy due to amyloid deposition with accompanying cardiac abnormalities
M Uehara, S Kuraishi, S Ikegami, H Oba… - The Journal of Spinal …, 2023 - Taylor & Francis
Background Amyloidosis is a rare group of diseases in which fibrillar amyloid proteins are
deposited in systemic organs to result in functional disorder. However, amyloidosis affecting …
deposited in systemic organs to result in functional disorder. However, amyloidosis affecting …
Cervical amyloidoma of transthyretin type: a case report and review of literature
MH MacLennan, A le Roux - BMC geriatrics, 2022 - Springer
Background Amyloidoma is a rare clinical entity characterized by the focal aggregation of
amyloid protein within the body, void of systemic involvement. To our knowledge, there have …
amyloid protein within the body, void of systemic involvement. To our knowledge, there have …
[HTML][HTML] AL amyloidosis manifesting as a vertebral amyloidoma secondary to an unrecognized plasmacytoma expressing cyclin D1 case report
JB Jones, N Lopez-Hisijos, RA Berkman… - International Journal of …, 2024 - Elsevier
Introduction Immunoglobin-related (AL) amyloidosis is the production of amyloidogenic
immunoglobulin light chains from clonal plasma cells or, rarely, B-cell lymphomas with …
immunoglobulin light chains from clonal plasma cells or, rarely, B-cell lymphomas with …
[PDF][PDF] Spinal Plasmacytoma Transformed Into Solitary Sacral Amyloidoma: A Case Report
Amyloidoma is a rare complication of plasmacytoma, that can involve the spine and present
with compressive neurological symptoms. It is usually a diagnosis of exclusion, and is …
with compressive neurological symptoms. It is usually a diagnosis of exclusion, and is …
[HTML][HTML] Surgically treated intradural spinal manifestation of hereditary amyloidogenic transthyretin amyloidosis-A case report and scoping review of the literature
S Voglis, Y Yildiz, F von Faber-Castell, KJ Harnisch… - Brain and Spine, 2022 - Elsevier
Abstract Introduction Hereditary transthyretin amyloidosis (ATTRv) is an autosomal-
dominant disorder, where a TTR mutations lead to amyloid fibril deposits in tissues and …
dominant disorder, where a TTR mutations lead to amyloid fibril deposits in tissues and …