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Journals / Marmara Medical Journal / 1999 / Cilt: 12 - Sayı: 2

CARDIAC AMYLOIDOSIS AS A COMPLICATION OF MULTIPLE MYELOMA

Sibel ERSAN
Refik DEMİRTUNÇ
Yıldırım ÇINAR
Pages
94–97
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

We described the clinical features and diagnostic approaches by review of the literature.Key Words : Cardiac amyloidosis, Multiple myeloma, Restrictive cardiomyopathy

📌 3 Key Takeaways

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Objective & Hypothesis:Restrictive cardiomyopathy due to cardiac amyloid deposition is not an uncommon complication of multiple myeloma.
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Key Findings & Data:Most cases of cardiac amyloidosis reported in early series were diagnosed postmortem at autopsy(1,2).The following is a report of a case with antemortem diagnosis of cardiac amyloidosis as a complication of multiple myeloma.
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Conclusion & Impact:We described the clinical features and diagnostic approaches by review of the literature.Key Words : Cardiac amyloidosis, Multiple myeloma, Restrictive cardiomyopathy
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Restrictive cardiomyopathy due to cardiac amyloid deposition is not an uncommon complication of multiple myeloma. Most cases of cardiac amyloidosis reported in early series were diagnosed postmortem at autopsy(1,2).The following is a report of a case with antemortem diagnosis of cardiac amyloidosis as a complication of multiple myeloma. We described the clinical features and diagnostic approaches by review of the literature.Key Words : Cardiac amyloidosis, Multiple myeloma, Restrictive cardiomyopathy

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Cite This Article

ERSAN, S., DEMİRTUNÇ, R., ÇINAR, Y. (1999). CARDIAC AMYLOIDOSIS AS A COMPLICATION OF MULTIPLE MYELOMA. Marmara Medical Journal, Cilt: 12 - Sayı: 2, 94–97. https://ajindex.com/articles/284210

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