Journal Information
Vol. 3. Issue 5.
Pages 233-236 (September - October 2007)
Share
Share
Download PDF
More article options
Vol. 3. Issue 5.
Pages 233-236 (September - October 2007)
Caso clínico
Full text access
Síndrome del canal carpiano como primera manifestación clínica de amilodosis AL primaria sistémica aislada
Carpal tunnel syndrome as a predictor of isolated systemic primary AL amyloidosis
Visits
10391
Joan Dalmau Carolà
Corresponding author
jdalmauc@acmcb.es

Correspondencia: Dr. J. Dalmau. Joan Maragall, 26. 17002 Girona. España.
Servei de Reumatologia. Clínica Girona. XHUP. Girona. España
This item has received
Article information

El diagnóstico del síndrome del canal carpiano, frecuente, rara vez va más allá de un estudio clínico y electromiográfico. Presentamos el caso de una mujer de 60 años diagnosticada de amiloidosis AL primaria sistémica muchos años después de que se hubiera manifestado el síndrome del canal carpiano.

Palabras clave:
Síndrome del canal carpiano
Amiloidosis
Amiloidosis AL primaria sistémica

The diagnosis of common carpal tunnel syndrome, usually relies only on clinical grounds and electromyographic study. We present a 60-year-old woman who was diagnosed with systemic primary AL amyloidosis many years after the carpal tunnel syndrome had begun.

Key words:
Carpal tunnel syndrome
Amyloidosis
Systemic primary AL amyloidosis
Full text is only aviable in PDF
Bibliografía
[1.]
D.C. Seldin, M. Skinner.
Arthritis accompanying systemic diseases.
7.a ed, pp. 1697-1704
[2.]
R.W. Sims, M.N. Prout, A.S. Cohen.
The epidemiology of AL and AA amyloidosis.
Bailliere Clin Rheumatol, 8 (1994), pp. 627-636
[3.]
R.S. Abraham, R.J. Clark, S.C. Bryant, J.F. Lymp, T. Larson, R.A. Kyle, et al.
Correlation of serum immunoglobulin free light chain quantification with urinary Bence Jones protein in light chain myeloma.
Clin Chem, 48 (2002), pp. 655-657
[4.]
M.T. Elghetany, A. Saleem.
Methods for staining amyloid in tissues: a review.
Stain Technol, 63 (1988), pp. 201-212
[5.]
E. Arbustini, P. Morbini, L. Verga, G. Merlini.
Light and electron microscopy immunohistochemical characterization of Amyloid deposits.
Amyloid - Int J Exp Clin Invest, 4 (1997), pp. 157-170
[6.]
A. Lim, J. Wally, M.T. Walsh, M. Skinner, C.E. Costello.
Identification and localization of a cysteinyl pottranslational modification in an amyloidogenic kappa 1 light chain protein by electrospray ionization and matrix-assisted laser desoption/desonisation mass spectrometry.
Anal Biochem, 295 (2001), pp. 45-56
[7.]
M. Skinner, J. Anderson, R. Simms, R. Falk, M. Wang, C. Libbey, et al.
Treatment of 100 patients with primary amyloidosis: a randomized trial of melphalan, prednisone, and colchicine versus colchicine only.
Am J Med, 100 (1996), pp. 290-298
[8.]
Resnick, G. Niwayama.
Diagnosis of bone and joint disorders.
2.a ed., Sauders, (1998),
[9.]
I.l. Van Gameren, B.P.C. Hazenberg, P.L. Jager, J.W. Smit, E. Vallenga.
AL amyloidosis treated with induction chemotherapy with VAD followed by hight dose melphalan and autologous stem cell transplantation.
Amyloid: J Protein Folding Disorders, 9 (2002), pp. 165-174
[10.]
M.B. Pepys, J. Herbert, W.L. Hutchinson, G.A. Tennent, H.J. Lachman, J.R. Gallimore, et al.
Targeted pharmalogical depletion of serum amyloid P component for treatment of human amyloidosis.
Nature, 417 (2002), pp. 254-259
Copyright © 2007. Elsevier España S.L Barcelona
Download PDF
Idiomas
Reumatología Clínica (English Edition)
Article options
Tools
es en

¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?