Systemic AL amyloidosis with an undetectable plasma cell dyscrasia: A zebra without stripes

Author:

Staron Andrew1ORCID,Kataria Yachana2,Murray David L.3,Sloan J. Mark1ORCID,Sanchorawala Vaishali1ORCID

Affiliation:

1. Amyloidosis CenterBoston University School of Medicine, Boston Medical Center Boston Massachusetts

2. Department of Pathology and Laboratory Medicine, Boston Medical CenterBoston University School of Medicine Boston Massachusetts

3. Laboratory Medicine and PathologyMayo Clinic Rochester Minnesota

Funder

School of Medicine, Boston University

Publisher

Wiley

Subject

Hematology

Reference7 articles.

1. Identification of Amyloidogenic Light Chains Requires the Combination of Serum-Free Light Chain Assay with Immunofixation of Serum and Urine

2. The utility of MASS-FIX to detect and monitor monoclonal proteins in the clinic

3. Splenic plasma cells can serve as a source of amyloidogenic light chains

4. SanjayK AngelaD SurendraD et al. Mass spectrometric approach to identify N‐glycosylation of light chain in patients with immunoglobulin light chain amyloidosis (AL). In: Proceedings of the AACR Annual Meeting; April 14–18 2018; Chicago IL.Cancer Res. 2018; 78 (abstr).2693.

5. MASS-FIX may allow identification of patients at risk for light chain amyloidosis before the onset of symptoms

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2. Sudden Death by AL Amyloidosis;American Journal of Forensic Medicine & Pathology;2023-02-04

3. Amyloidosis;A Clinician's Pearls & Myths in Rheumatology;2023

4. Amyloidosis and the Kidney: An Update;Seminars in Nephrology;2022-11

5. Beyond Survival in AL amyloidosis: Identifying and Satisfying Patients’ Needs;Hemato;2022-01-04

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