J Cardiovasc Ultrasound.  2012 Dec;20(4):209-212. 10.4250/jcu.2012.20.4.209.

Familial Transthyretin Amyloidosis with Variant Asp38Ala Presenting with Orthostatic Hypotension and Chronic Diarrhea

Affiliations
  • 1Division of Cardiology, Department of Internal Medicine, Kyungpook National University Hospital, Daegu, Korea. ddhyang@knu.ac.kr

Abstract

A 53-year-old man complained of orthostatic, non-rotating dizziness, and chronic watery diarrhea of several years duration. His nerve-conduction velocity test revealed peripheral sensory-motor polyneuropathy and he showed an autonomic function abnormality. Echocardiographic examination showed ventricular and atrial wall thickening with a granular "sparkling" appearance. Left ventricular systolic function was preserved but pseudonormal diastolic dysfunction was present. Coronary angiography showed normal coronary arteries and an endomyocardial biopsy revealed lesions consistent with cardiac amyloidosis. Colonoscopic biopsy also revealed the deposition of amyloid fibrils. Gene analysis found the transthyretin variant Asp38Ala. His son had same mutation, but three daughters did not. In conclusion, we report a case of familial transthyretin amyloidosis with Asp38Ala.

Keyword

Amyloidosis; Transthyretin; Asp38Ala; Orthostatic hypotension; Polyneuropathy

MeSH Terms

Amyloid
Amyloid Neuropathies, Familial
Amyloidosis
Biopsy
Coronary Angiography
Coronary Vessels
Diarrhea
Dizziness
Hypotension, Orthostatic
Nuclear Family
Polyneuropathies
Prealbumin
Amyloid
Amyloid Neuropathies, Familial
Prealbumin

Figure

  • Fig. 1 Two-dimensional transthoracic echocardiography. Biventricular hypertrophy and the thickened inter-atrial septum are shown in a parasternal long-axis view (A), four-chamber view (B and C).

  • Fig. 2 Pulse-waved Doppler echocardiogram (A) and tissue Doppler echocardiogram (B) showing and elevated E/Ea ratio and low mitral annulus velocities, suggestive of diastolic dysfunction with a pseudonormal pattern.

  • Fig. 3 Light microscopy finding of tissue obtained by cardiac biopsy (haematoxylin and eosin stained, original magnification × 40). Amyloid appears as pink-hyaline extracellular deposits (black arrows) between myocytes and in blood vessels.

  • Fig. 4 Electron microscopy of cardiac tissue. Electron microscopy demonstrated fibrils typical of amyloid at the edge of a myocytes (A). The edge of a myocyte (lower left) and above it is a mass of amyloid fibrils (B).

  • Fig. 5 Transthyretin gene analysis in the patient and his offspring (A: patient, B: daughter 1, C: daughter 2, D: daughter 3, E: son). A: The patient was diagnosed as transthyretin amyloidosis (ATTR) variant Asp38Ala. E: The patient's offspring were screening for ATTR, but only his son had the same mutation.


Reference

1. Falk RH, Comenzo RL, Skinner M. The systemic amyloidoses. N Engl J Med. 1997. 337:898–909.
Article
2. Westermark P, Benson MD, Buxbaum JN, Cohen AS, Frangione B, Ikeda S, Masters CL, Merlini G, Saraiva MJ, Sipe JD. Amyloid fibril protein nomenclature -- 2002. Amyloid. 2002. 9:197–200.
3. Westermark P, Benson MD, Buxbaum JN, Cohen AS, Frangione B, Ikeda S, Masters CL, Merlini G, Saraiva MJ, Sipe JD. A primer of amyloid nomenclature. Amyloid. 2007. 14:179–183.
Article
4. Ando Y, Nakamura M, Araki S. Transthyretin-related familial amyloidotic polyneuropathy. Arch Neurol. 2005. 62:1057–1062.
Article
5. Falk RH, Dubrey SW. Amyloid heart disease. Prog Cardiovasc Dis. 2010. 52:347–361.
Article
6. Shah KB, Inoue Y, Mehra MR. Amyloidosis and the heart: a comprehensive review. Arch Intern Med. 2006. 166:1805–1813.
7. Rapezzi C, Perugini E, Salvi F, Grigioni F, Riva L, Cooke RM, Ferlini A, Rimessi P, Bacchi-Reggiani L, Ciliberti P, Pastorelli F, Leone O, Bartolomei I, Pinna AD, Arpesella G, Branzi A. Phenotypic and genotypic heterogeneity in transthyretin-related cardiac amyloidosis: towards tailoring of therapeutic strategies? Amyloid. 2006. 13:143–153.
Article
8. Merlini G, Bellotti V. Molecular mechanisms of amyloidosis. N Engl J Med. 2003. 349:583–596.
Article
9. Smith TJ, Kyle RA, Lie JT. Clinical significance of histopathologic patterns of cardiac amyloidosis. Mayo Clin Proc. 1984. 59:547–555.
Article
10. Falk RH. Diagnosis and management of the cardiac amyloidoses. Circulation. 2005. 112:2047–2060.
Article
11. Rahman JE, Helou EF, Gelzer-Bell R, Thompson RE, Kuo C, Rodriguez ER, Hare JM, Baughman KL, Kasper EK. Noninvasive diagnosis of biopsy-proven cardiac amyloidosis. J Am Coll Cardiol. 2004. 43:410–415.
Article
12. Benson MD, Uemichi T. Transthyretin amyloidosis. Amyloid Int J Exp Clin Invest. 1996. 3:44–56.
Article
13. Ikeda S, Hanyu N, Hongo M, Yoshioka J, Oguchi H, Yanagisawa N, Kobayashi T, Tsukagoshi H, Ito N, Yokota T. Hereditary generalized amyloidosis with polyneuropathy. Clinicopathological study of 65 Japanese patients. Brain. 1987. 110(Pt 2):315–337.
Article
14. Benson MD, Kincaid JC. The molecular biology and clinical features of amyloid neuropathy. Muscle Nerve. 2007. 36:411–423.
Article
15. Conceição I, De Carvalho M. Clinical variability in type I familial amyloid polyneuropathy (Val30Met): comparison between late- and early-onset cases in Portugal. Muscle Nerve. 2007. 35:116–118.
Article
16. Bittencourt PL, Couto CA, Clemente C, Farias AQ, Palácios SA, Mies S, Goldberg AC. Phenotypic expression of familial amyloid polyneuropathy in Brazil. Eur J Neurol. 2005. 12:289–293.
Article
17. Ikeda S, Nakazato M, Ando Y, Sobue G. Familial transthyretin-type amyloid polyneuropathy in Japan: clinical and genetic heterogeneity. Neurology. 2002. 58:1001–1007.
Article
18. Suhr OB, Svendsen IH, Andersson R, Danielsson A, Holmgren G, Ranløv PJ. Hereditary transthyretin amyloidosis from a Scandinavian perspective. J Intern Med. 2003. 254:225–235.
Article
19. Yazak M, Take YI, Katoh M, Ikeda SI. Postmortem findings in two familial amyloidosis patients with transthyretin variant Asp38Ala. Amyloid. 2000. 7:270–277.
Article
20. Tachibana N, Tokuda T, Yoshida K, Taketomi T, Nakazato M, Li YF, Masuda Y, Ikeda S. Usefulness of MALDI/TOF mass spectrometry of immunoprecipitated serum variant transthyretin in the diagnosis of familial amyloid polyneuropathy. Amyloid. 1999. 6:282–288.
Article
21. Kishikawa M, Nakanishi T, Miyazaki A, Shimizu A, Kusaka H, Fukui M, Nishiue T. A new amyloidogenic transthyretin variant, [D38A], detected by electrospray ionization/mass spectrometry. Amyloid. 1999. 6:278–281.
Article
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