Systemic heavy- and light-chain amyloidosis presenting nephrotic syndrome and congestive heart failure: a case presentation and literature review
Author:
Affiliation:
1. Hidaka Hospital, Kidney Disease and Dialysis Center, Gunma, Japan;
2. Department of General Internal Medicine, Takasaki General Medical Center, Gunma, Japan;
3. Hidaka Hospital, Hidaka Center for Pathologic Diagnosis and Research, Gunma, Japan
Publisher
Informa UK Limited
Subject
Internal Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/13506129.2019.1582022
Reference7 articles.
1. Co-deposition of amyloidogenic immunoglobulin light and heavy chains in localized pulmonary amyloidosis
2. IgG1λ light and heavy chain renal amyloidosis
3. Mass Spectrometry–Based Proteomic Diagnosis of Renal Immunoglobulin Heavy Chain Amyloidosis
4. The diagnosis and characteristics of renal heavy-chain and heavy/light-chain amyloidosis and their comparison with renal light-chain amyloidosis
5. Heavy and Light chain amyloidosois presenting as complete heart block: A rare presentation of a rare disease
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1. Development of diagnostic antibodies against immunoglobulin heavy chain variable region for heavy chain amyloidosis (AH amyloidosis);Pathology International;2021-03-13
2. IgGκ light and heavy chain amyloidosis secondary to a B‐cell lymphoproliferative disorder, whole picture on a renal biopsy;Nephrology;2020-05
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