Results 11 to 20 of about 5,095,980 (121)

Localized Immunoglobulin Light-Chain Amyloidosis of the Ulnar Nerve [PDF]

open access: yesCase Reports in Neurology, 2021
Amyloidosis is a disorder caused by extracellular tissue deposition of insoluble fibrils. Amyloidosis can be divided into systemic or localized disease. Primary systemic amyloidosis is a multisystem disease caused by the deposition of amyloid in various ...
Shinsuke Morisaki   +5 more
doaj   +2 more sources

Localized Lymph Node Light Chain Amyloidosis [PDF]

open access: yesCase Reports in Hematology, 2015
Immunoglobulin-derived light chain amyloidosis can occasionally be associated with localized disease. We present a patient with localized lymph node light chain amyloidosis without an underlying monoclonal protein or lymphoproliferative disorder and ...
Binod Dhakal   +3 more
doaj   +2 more sources

Bilateral atrial appendage thrombosis in light chain cardiac amyloidosis: a case report

open access: yesFrontiers in Cardiovascular Medicine
Light chain cardiac amyloidosis (AL-CA) is a severe and progressively infiltrative disease caused by the deposition of misfolded monoclonal immunoglobulin light chains in the myocardial extracellular space.
Haiyan Jia   +4 more
doaj   +2 more sources

Cutaneous light chain amyloidosis with multiple myeloma: A concise review

open access: yesHematology/Oncology and Stem Cell Therapy, 2019
Objective/Background: Cutaneous immunoglobulin (Ig) amyloid light-chain (AL) amyloidosis associated with overt multiple myeloma (MM) is rare and optimal treatment is not well defined.
Mirela Andrei, Jen Chin Wang
doaj   +2 more sources

Concurrent light chain amyloidosis and proximal tubulopathy: Insights into different aggregation behavior—A case report

open access: yeseJHaem, 2022
Due to differences in the protein folding mechanisms, it is exceedingly rare for amyloid light chain (AL) amyloidosis and monoclonal gammopathy of renal significance (MGRS) to coexist.
Simone Feurstein   +13 more
doaj   +2 more sources

Recent advances in understanding and treating immunoglobulin light chain amyloidosis [version 1; referees: 2 approved] [PDF]

open access: yesF1000Research, 2018
Immunoglobulin (Ig) light chain (AL) amyloidosis is a clonal plasma cell disorder characterized by misfolded Ig light chain deposition in vital organs of the body, resulting in proteotoxicity and organ dysfunction.
Talha Badar   +2 more
doaj   +2 more sources

Suggestive Diagnostic Process in a Case of Multiple Myeloma with Gastrointestinal Immunoglobulin Light-Chain Amyloidosis Accompanied by Protein-Losing Enteropathy

open access: yesCase Reports in Gastrointestinal Medicine, 2021
Multiple myeloma is a type of plasma cell neoplasm that produces monoclonal immunoglobulin. Multiple myeloma is known to cause immunoglobulin light-chain (AL) amyloidosis, which frequently involves the kidney and heart.
Katsuya Endo   +15 more
doaj   +2 more sources

Virtual Screening for Promising Kinetic Stabilizers of Light Chains in Immunoglobulin Light Chain Amyloidosis Through Drug Repurposing [PDF]

open access: yes, 2023
In immunoglobulin light chain amyloidosis, unstable immunoglobulin light chains aggregate as amyloid fibrils in organs, leading to organ failure and death in more than 50% of untreated patients. Research by Morgan et al. (Morgan, G. J. et.
Jonas, Jeppesen   +3 more
core   +2 more sources

Localized Lymph Node Light Chain Amyloidosis [PDF]

open access: yes, 2020
The prognosis of systemic amyloid light chain (AL) amyloidosis is generally poor, hence requiring chemotherapy or hematopoietic stem cell transplantation, while the prognosis of localized AL amyloidosis without an abnormal monoclonal immunoglobulin light
Yamashita, Taro   +4 more
core   +2 more sources

Immunoglobulin light-chain amyloidosis mimicking bulbar amyotrophic lateral sclerosis

open access: yes, 2023
Immunoglobulin light-chain amyloidosis mimicking bulbar amyotrophic lateral ...
Antoine Pegat (16266978)   +1 more
core   +1 more source

Home - About - Disclaimer - Privacy