[HTML][HTML] Clinical characterization and outcomes of a cohort of colombian patients with AL Amyloidosis

JA Lacouture Fierro, DA Ribero Vargas… - Colombia …, 2023 - scielo.org.co
Background: Amyloid light chain (AL) amyloidosis is characterized by amyloid fibril
deposition derived from monoclonal immunoglobulin light chains, resulting in multiorgan …

Noncardiac Manifestations of Hereditary Amyloidosis

SL Khella - The American Journal of Cardiology, 2022 - Elsevier
The most common forms of cardiac amyloidosis are progressive, life threatening, and
underrecognized. Symptoms affect a variety of organs and overlap with those of more …

[HTML][HTML] Advanced case of cardiac amyloidosis presents with chronic diarrhea

M Abdelsamia, O Mosalem, Y Radwan… - Cureus, 2022 - ncbi.nlm.nih.gov
Late diagnosis of light chain (AL) amyloidosis can lead to catastrophic consequences on the
quality of life of affected patients and overall disease prognosis. Therefore, clinicians should …

Quick consults in hematology: Staging and treating immunoglobulin light chain (AL) amyloidosis

M Gertz - American journal of hematology, 2023 - Wiley Online Library
A 67-year-old man was found to have proteinuria on a Medicare annual physical. He is
referred to a nephrologist who performed a kidney biopsy showing amyloidosis confirmed to …

[HTML][HTML] Rapidly Progressive Myopathy: Unveiling Light Chain Amyloidosis as an Initial Manifestation of Multiple Myeloma. A Case Report and Literature Review

P Kaminskiene, T Stojkovic, D Roos-Weil… - Neuromuscular …, 2024 - Elsevier
We present the case of a 79-year-old man with rapidly progressive myopathy as the initial
manifestation of light chain amyloidosis associated with multiple myeloma. The patient …

Kidney Amyloidosis: Updates on Pathogenesis and Therapeutic Frontiers

CECMG Atta - 2024 - karger.com
Background: Amyloidosis includes a diverse group of rare diseases characterized by the
misfolding of native or mutant proteins, leading to extracellular accumulation in various …

Clinical presentation, laboratory manifestations, and diagnosis of immunoglobulin light chain (AL) amyloidosis

A Dispenzieri, RJ Glassock - 2020 - uptodate.com
Amyloidosis is a generic term that refers to the extracellular tissue deposition of fibrils
composed of subunits of a variety of normal serum proteins. These fibrils have a …

[PDF][PDF] Caracterización clínica y desenlaces de una cohorte de pacientes colombianos con amiloidosis AL

CSO Ospina - Colombia Médica, 2023 - redalyc.org
Antecedentes: La amiloidosis por amiloide de cadenas ligeras (AL) se caracteriza por el
depósito de fibrillas amiloides derivadas de cadenas ligeras de inmunoglobulinas …

Unusual presentation of transthyretin (ATTR) cardiac amyloidosis: A case report of pruritus as a possible initial symptom and challenging diagnosis

M Baghaee, M Mohammadi, A Moradi… - Clinical Case …, 2023 - Wiley Online Library
Key Clinical Message This case emphasizes the significance of cardiac amyloidosis as a
potential diagnosis in individuals manifesting with lesion‐free pruritus and normal liver tests …

[HTML][HTML] Modified Body Mass Index as a Novel Nutritional and Prognostic Marker in Patients with Cardiac Amyloidosis

F Dongiglio, G Palmiero, E Monda, M Rubino, F Verrillo… - Cardiogenetics, 2022 - mdpi.com
The nutritional assessment is gaining clinical relevance since cardiac cachexia and
malnutrition are emerging as novel markers of functional status and prognosis in many …