Primary ( <scp>AL</scp> ) Amyloidosis Following <scp>COVID</scp> ‐19 Infection: A Case Report

Primary (AL) amyloidosis is a rare systemic disorder caused by extracellular deposition of monoclonal immunoglobulin light chains, resulting in multi-organ dysfunction. SARS-CoV-2 infection may induce persistent inflammatory and immune dysregulation, potentially promoting amyloid formation, although clinical evidence is limited, making the recognition of post-COVID-19 amyloidosis clinically relevant and potentially novel. A 39-year-old Caucasian male presented with progressive weight loss (18 kg over 6 months), epigastric pain, early satiety, and hepatosplenomegaly. Ten months prior, he had recovered from COVID-19 with mild pulmonary involvement. Initial ultrasonography and endoscopy were unremarkable except for mild gastritis. Subsequent imaging revealed hepatosplenomegaly (liver: 200 mm; spleen: 157 mm) and cholestatic liver enzyme elevation. Investigations for sclerosing cholangitis were negative. Liver biopsy with Congo red staining confirmed amyloid deposition, and bone marrow analysis revealed clonal plasma cells, establishing primary (AL) amyloidosis. Echocardiography showed left ventricular hypertrophy (LVH) due to amyloid infiltration. This case underscores a possible association between SARS-CoV-2 infection and primary amyloidosis. Post-COVID inflammatory responses, elevated serum amyloid A, oxidative stress, and hypercoagulability may collectively facilitate amyloidogenic peptide formation and tissue deposition. Molecular dynamics studies further support the plausibility of SARS-CoV-2-induced amyloidogenesis. Primary amyloidosis may develop following COVID-19. Clinicians should consider amyloidosis in patients with unexplained weight loss, hepatosplenomegaly, or cholestatic liver enzyme abnormalities after SARS-CoV-2 infection. Early biopsy and type-specific diagnosis are essential for timely management. This case highlights the potential clinical significance of a post-COVID-19 association, as primary amyloidosis may develop following COVID-19.

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Publication Details

Journal
Clinical Case Reports
Published
2026-01-28
DOI
https://doi.org/10.1002/ccr3.71871
Primary Topic
Amyloidosis: Diagnosis, Treatment, Outcomes
Type
article
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article

Primary ( AL ) Amyloidosis Following COVID ‐19 Infection: A Case Report

Sepideh Tahsini Tekantapeh, Amirreza Khalaji, Nasrin Gholami, Gholamrez Ravaei et al.
Clinical Case Reports
Amyloidosis: Diagnosis, Treatment, Outcomes
article

Primary ( AL ) Amyloidosis Following COVID ‐19 Infection: A Case Report

Sepideh Tahsini Tekantapeh, Amirreza Khalaji, Nasrin Gholami, Gholamrez Ravaei, Babak Nejati
article en

Abstract

Primary (AL) amyloidosis is a rare systemic disorder caused by extracellular deposition of monoclonal immunoglobulin light chains, resulting in multi-organ dysfunction. SARS-CoV-2 infection may induce persistent inflammatory and immune dysregulation, potentially promoting amyloid formation, although clinical evidence is limited, making the recognition of post-COVID-19 amyloidosis clinically relevant and potentially novel. A 39-year-old Caucasian male presented with progressive weight loss (18 kg over 6 months), epigastric pain, early satiety, and hepatosplenomegaly. Ten months prior, he had recovered from COVID-19 with mild pulmonary involvement. Initial ultrasonography and endoscopy were unremarkable except for mild gastritis. Subsequent imaging revealed hepatosplenomegaly (liver: 200 mm; spleen: 157 mm) and cholestatic liver enzyme elevation. Investigations for sclerosing cholangitis were negative. Liver biopsy with Congo red staining confirmed amyloid deposition, and bone marrow analysis revealed clonal plasma cells, establishing primary (AL) amyloidosis. Echocardiography showed left ventricular hypertrophy (LVH) due to amyloid infiltration. This case underscores a possible association between SARS-CoV-2 infection and primary amyloidosis. Post-COVID inflammatory responses, elevated serum amyloid A, oxidative stress, and hypercoagulability may collectively facilitate amyloidogenic peptide formation and tissue deposition. Molecular dynamics studies further support the plausibility of SARS-CoV-2-induced amyloidogenesis. Primary amyloidosis may develop following COVID-19. Clinicians should consider amyloidosis in patients with unexplained weight loss, hepatosplenomegaly, or cholestatic liver enzyme abnormalities after SARS-CoV-2 infection. Early biopsy and type-specific diagnosis are essential for timely management. This case highlights the potential clinical significance of a post-COVID-19 association, as primary amyloidosis may develop following COVID-19.

Clinical Case ReportsVol. 14(2)
Tabriz University of Medical Sciences (IR)
Good health and well-being
Openalex Percentile: Top 75%
Amyloidosis: Diagnosis, Treatment, Outcomes
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