KaydedilenlerDerginizi ekleyin

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

CARDIAC AMYLOIDOSIS AS A COMPLICATION OF MULTIPLE MYELOMA

Sibel ERSAN
Refik DEMİRTUNÇ
Yıldırım ÇINAR
Sayfa
94–97
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

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

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Restrictive cardiomyopathy due to cardiac amyloid deposition is not an uncommon complication of multiple myeloma.
📊
Temel Bulgular & Veri: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.
💡
Sonuç & Katkı:We described the clinical features and diagnostic approaches by review of the literature.Key Words : Cardiac amyloidosis, Multiple myeloma, Restrictive cardiomyopathy
🔬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.Key Words : Cardiac amyloidosis, Multiple myeloma, Restrictive cardiomyopathy

🔖

Bu Makaleye Atıf Yap

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

Kaynakça (10)

  1. O'Connell JB, Renland DO. Myocarditis and specific myocardial diseases. In: Schlant RC, Alexander RW, O'Rourke RA, et al (eds). Hurst's The Heart, 8^’ ed. Hew York, McGraw-Hill, 1994:1591 -1607. Dubrey SIV, Cha R, Anderson J, et at. The clinical features of immunoglobulin light-chain (AL) amyloidosis with heart involvement (abstract). QJM 1998;91:141-157. 6 Marmara Medical Journal Volume 12 No 2 April 1999
  2. Vaitkus PT, Kussmaul WG. Constrictive pericarditis versus restrictive cardiomyopathy: a reappraisal and update of diagnostic criteria. Am Heart J 1991;122:1431-1441.
  3. Hamer JP, Janssen S, Rijswijk van MH, Lie Kl. Amyloid cardiomyopathy in systemic non-hereditary amyloidosis. Clinical, échocardiographie and electrocardiographic findings in 30 patients with AA and 24 patients with AL amyloidosis. Eur Heart J 1992;13:623-627.
  4. Schattner A, Epstein M, Berrebi A, Caspi A. Case report: multiple myeloma presenting as a diastolic heart failure with no evidence of amyloidosis. Am J Med Sci 1995;310:256-257.
  5. Mitchell MA, Horneffer MD. Standiford TJ. Multiple myeloma complicated by restrictive cardiomyopathy and cardiac tamponade. Chest 1993;103:946-947.
  6. Gertz MA, Kyle RA. Primary systemic amyloidosis-a diagnostic primer. Mayo Clin Proc 1989;64:1505- 1519. Reisinger J, Dubrey SW, Lavalley M, Skinner M, Falk RH. Electrophysiologic abnormalities in AL (primary) amyloidosis with cardiac involement. J Am Coll Cardiol 199 7;30:1046-1051.
  7. Brandt K, Cathead E 5, Cohen A S. A clinical analysis of the course and prognosis of forty-two patients with amyloidosis. Am J Med 1968:44:955- 969. Klein AL, Hatle LK, Taliercio CP, et al. Prognostic significance of Doppler measures of diastolic function in cardiac amyloidosis. A Doppler echocardiography study. Circulation 1991:83:808- 816. Falk RH, Plehn JF, Deering T, et al. Sensitivity and specificity of the échocardiographie features of cardiac amyloidosis. Am J Cardiol 1987;59:418- 422. Simons M, Isner JM. Assessment of relative sensitivities of noninvasive tests for cardiac amyloidosis in documented cardiac amyloidosis. Am J Cardiol 1992;69:425-427.
  8. Dubrey SW, Cha K, Skinner M, La Valley M, Falk RH. Familial and primary (AL) cardiac amyloidosis: echocardiographically similar diseases with distinctly different clinical outcomes. Heart 1997;78:74-82.
  9. Hesse A, Altland K, Linke RP, et al. Cardiac amyloidosis: a review and report of a new transthyretin (prealbumin) variant. Br Heart J 1993;70:1 I 1-115.
  10. Tei C, Dujardin KS, Hodge DO, Kyl