Cardiac amyloidosis diagnosed by endomyocardial biopsy. Clinical, histopathological, immunohistochemical and ultrastructural studies;Amyloidoza serca rozpoznana na podstawie biopsji endomiokardialnej: Obraz klinicznyy, histopatologiczny, immunohistochemiczny i ultrastrukturalny

Kardiologia Polska

Volumn 63, Issue 1, 2005, Pages 20-35

  Prochorec Sobieszek, Monika ^a   Bilińska, Zofia T ^b,c   Grzybowski, Jacek ^b,c   Michalak, Ewa ^b,c   Jakubowska, Ewa ^b,c   Sobieszczańska Małek, Małgorzata ^b,c   Deptuch, Tomasz ^b,c   Walczak, Ewa ^a   Wagner, Teresa ^a   Walski, Michał ^b   Rózański, Jacek ^b,c   Kiedrowski, Mirosław ^a   Lubiszewska, Barbara ^b,c   Hoffman, Piotr ^b,c   Ruzyłło, Witold ^b,c  

^a INSTITUTE OF RHEUMATOLOGY   (Poland)

^b POLISH ACADEMY OF SCIENCES   (Poland)

^c Stefana Kardyna a Wyszy skiego w Warszawie   (Poland)

Author keywords

Cardiac amyloidosis; Electron microscopy; Endomyocardial biopsy; Immunohistochemistry

Indexed keywords

AMYLOID; PREALBUMIN;

ADULT; AGED; ARTICLE; CASE REPORT; CELL ULTRASTRUCTURE; CLINICAL FEATURE; CORRELATION ANALYSIS; DIAGNOSTIC VALUE; ELECTRON MICROSCOPY; FEMALE; HEART AMYLOIDOSIS; HEART MUSCLE BIOPSY; HEREDITY; HISTOCHEMISTRY; HISTOPATHOLOGY; HOSPITALIZATION; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; PARAMETER; PERICARDIOTOMY; SURVIVAL TIME;

EID: 23844482082     PISSN: 00229032     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (20)

1. Serpell L.C., Sunde M., Blake C.C.: The molecular basis of amyloidosis. Cell. Mol. Life Sci. 1997, 53, 871-887.
2. Kyle R.A.: Amyloidosis. Circulation. 1995, 91, 1269-1271.
3. McCarthy R.E. Kasper E.K.: A review of the amyloidoses that infiltrate the heart. Clin. Cardiol. 1998, 21, 547-552.
4. Lachmann H.J., Booth D.R., Booth S.E. et al.: Misdiagnosis or hereditary amyloidosis as AL (primary) amyloidosis. N. Engl. J. Med. 2002, 346, 1786-91.
5. Pereira N.L., Dec G.W.: Restrictive and infiltrative cardiomyopathies. w Eds: M.H. Crawford, J.P. Marco, W.J. Paulus: Cardiology 2nd Edition, Edinburgh, 2004, 983-992.
6. D'Amati G., Factor S.M.: Endomyocardial biopsy findings in patients with ventricular arrhythmias of unknown origin. Cardiovasc. Pathol. 1996, 5, 139-144.
7. Von Kemp K., Beckers R., Vandenweghe J. et al.: Echocardiography and magnetic resonance imaging in cardiac amyloidosis. Acta Cardiol. 1989, 44, 29-36.
8. Smith T.J., Kyle R.A., Lie J.T.: Clinical significance of histopathological patterns of cardiac amyloidosis. Mayo Clin. Proc. 1984, 59, 547-555.
9. Dubrey S.W., Cha K., Anderson J. et al.: The clinical features of immunoglobulin light-chain (AL) amyloidosis with heart involvement. Q.J.M. 1998, 91, 141-157.
10. Hattori T., Takei Y., Koyama J.: Clinical and pathological studies of cardiac amyloidosis in transthyretin type familial amyloid polyneuropathy. Amyloid 2003, 10(4), 229-232.
11. Falk R.H., Comenzo R.L., Skinner M.: The systemic amyloidoses. N. Engl. J. Med. 1997, 25, 898-909.
12. Dubrey S.W., Cha K., Skinner M. et al.: Familial and primary (AL) amyloidosis: echocardiographically similar diseases with distinctly different clinical outcomes. Heart 1997, 78, 74-82.
13. Gertz M.A., Kyle R.A., Thibodeau S.N.: Familial amyloidosis: a study of 52 North American-born patients examined during a 30-year period. Mayo Clin. Proc. 1991, 67, 428-40.
14. Skinner M., Sanchorawala V., Seldin D.C. et al.: High dose melphalan and autologous steam-cell transplantation in patient with AL, amyloidosis: an 8-year study. Ann. Intern. Med. 2004, 140, 85-93.
15. Holmgren G., Ericzon B.G., Groth C.G. et al: Clinical improvement and amyloid regression after liver transplantation in hereditary transthyretin amyloidosis. Lancet 1993, 341, 113-6.
16. Scully R.E., Mark E.J., Mc Neely B.V.: Case records of the Massachusetts General Hospital. Case 30-1982. N. Engl. J. Med. 1982, 302, 298-303.
17. Crotty T.B., Li Ch.Y., Edwards W.D. et al.: Amyloidosis and endomyocardial biopsy: correlation of extent and pattern of deposition with amyloid immunophenotype in 100 cases. Cardiovasc. Pathol. 1995, 4, 39-42.
18. Strrkel S., Schneider H.M., Thoenes W.: Manifestation and ultrastructural typing of amyloid deposits in the heart. Virchows Arch [Pathol Anat] 1983, 401, 185-201.
19. Arbustini E., Merlini G., Gavazzi A. et al.: Cardiac immunocyte derived (AL) amyloidosis: An endomyocardial biopsy study in 11 patients. Am. Heart J. 1995, 130, 528-536.
20. Benson M.D.: The hereditary amyloidoses. Best Practice & Research Clinical Rheumathology 2003, 17, 909-927.