Hidden amyloidosis in liver and bone marrow

Author:

Jagadish Gayathri1,Archana M.2,Nataraj K. S.3,Desai Sandeep4,Kurpad Vishnu5

Affiliation:

1. Department of Hematopathology, Sri Shankara Cancer Hospital and Research Center, Bengaluru, Karnataka, India,

2. Department of Oncopathology, Sri Shankara Cancer Hospital and Research Center, Bengaluru, Karnataka, India,

3. Department of Hematology, Sri Shankara Cancer Hospital and Research Center, Bengaluru, Karnataka, India,

4. Department of Radiology, Sri Shankara Cancer Hospital and Research Center, Bengaluru, Karnataka, India,

5. Department of Surgical Oncology, Sri Shankara Cancer Hospital and Research Center, Bengaluru, Karnataka, India,

Abstract

Primary amyloidosis and multiple myeloma (MM) involve clonal plasma cell proliferation. Approximately 10–15% of patients with amyloidosis have MM. Characteristic apple-green birefringence using Congo red staining on polarized microscopy confirms amyloid. MM is prevalent at ages from 60 to 70 years. Amyloidosis commonly affects the heart, kidneys, gastrointestinal tract/liver and peripheral or autonomic nervous system predicting a poor prognosis due to organ deterioration. This case highlights the importance of diagnosing amyloidosis in a 60-year-old female where plasma cells were present in the liver and bone marrow along with amyloid deposits and for early initiation of intense chemotherapy.

Publisher

Scientific Scholar

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