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

Cardiac amyloidosis as a complication of multiple myeloma

Sayfa
94–97
Yayın Tarihi
2022-10-17
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

We described the clinical features and diagnostic approaches by review of the literature.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Restrictive cardiomyopathy due to cardiac amyloid deposition is not an uncommon complication of multiple myeloma.
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Temel Bulgular & Veri:Most cases of cardiac amyloidosis reported in early series were diagnosed postmortem at autopsy(1,2).
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Sonuç & Katkı:We described the clinical features and diagnostic approaches by review of the literature.
🔬Tür:Literatür & Derleme Çalışması
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

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.

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Bu Makaleye Atıf Yap

ERSAN, S., ÇINAR, Y., DEMİRTUNÇ, R. (2022). Cardiac amyloidosis as a complication of multiple myeloma. Marmara Medical Journal, Cilt: 12 - Sayı: 2, 94–97. https://ajindex.com/articles/578518

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