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Vol. 36. Issue 4.
Pages 225-227 (April 2000)
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Vol. 36. Issue 4.
Pages 225-227 (April 2000)
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Discinesia ciliar primaria. Una nueva variante fenotípica
Primary ciliary dyskinesia: a new phenotype
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J.A. Carretero Graciaa,*, A. Uliarte Raneab, J.M. Martínez-Peñuela Virsedac
a Servicios de Medicina Interna (Neumología). Hospital General de Soria
b Sección de Cuidados Intensivos. Hospital General de Soria
c Servicio de Anatomía Patológica. Hospital de Navarra
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La discinesia ciliar primaria (DCP) es un trastorno genético caracterizado por una incapacidad del batido ciliar, que cursa clínicamente con sinusitis y otitis de repetición, bronquitis crónica o recurrente e infertilidad en el varón. Aunque se han descrito diversas variantes fenotípicas, no es frecuente que el deterioro de la función pulmonar, secundario a la presencia de bronquiectasias, llegue a ser muy grave. Tampoco es conocido que las infecciones de las vías respiratorias altas pasen desapercibidas.

Presentamos un caso de DCP caracterizado por inmotilidad espermática, grave trastorno ventilatorio obstructivo, que requirió un trasplante bipulmonar secuencial, y ausencia objetiva de sinusitis u otitis recurrentes.

Palabras clave:
Discinesia ciliar primaria
Bronquiectasias
Trasplante pulmonar

Primary ciliary dyskinesia (PCD) is a genetic disorder characterized by the inability of ciliated structures to beat effectively. Clinical course includes recurrent sinus and ear infections, chronic or recurrent bronchitis and infertility in men. Although several phenotypes have been described, lung function deterioration secondary to bronchiectasis becomes severe only rarely. That upper airway tract infections go unnoticed has not been reported.

We report a case of PCD characterized by immotile sperm, severe obstructive respiratory disorder that required a sequential double lung transplant with the absence of recurrent sinus and ear infections.

Key words:
Primary ciliary dyskinesia
Bronchiectasis
Lung transplantation
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Bibliografía
[1.]
B.A. Afzelius.
A human syndrome caused by inmotile cilia.
Science, 193 (1976), pp. 317-319
[2.]
L.B. Holmes, J.B. Blennerhasset, K.F. Austen.
A reappraisal of Kartagener's Syndrome.
Am J Med Sci, 25 (1968), pp. 13-28
[3.]
M. Kartagener.
Zur Pathologie der Bronchiektasien: Bronchiektasien bei situs viscerum inversus.
Beitr Klin Tuberk, 83 (1933), pp. 489-501
[4.]
B. Mossberg, P. Camner.
Impaired mucociliary transport as a pathogenic factor in obstructive pulmonary diseases.
Chest, 77 (1980), pp. 265-266
[5.]
H. Kolberg, B. Mossberg, B.A. Afzelius, K. Phillipson, P. Camner.
Cystic fibrosis compared with inmotile cilia syndrome.
Scand J Respir Dis, 59 (1978), pp. 297-306
[6.]
B.A. Afzelius.
Inmotile cilia syndrome and ciliary abnormalities induced by infection and injury.
Am Rev Respir Dis, 124 (1981), pp. 107-109
[7.]
J.A.P. Turner, C.W.B. Corkey, J.Y.C. Lee, H. Levison, J.M. Sturgess.
Clinical expressions of the inmotile cilia syndrome.
Pediatrics, 67 (1981), pp. 805-810
[8.]
J. Chao, J.A. Turner, J.M. Sturgess.
Genetic heterogeneity of dyneindeficiency in cilia from patients with respiratory disease.
Am Rev Respir Dis, 126 (1982), pp. 302-305
[9.]
M.S. Jonsson, J.R. McCormick, C.G. Gillies, B. Gondos.
Kartagener's syndrome with motile spermatozoa.
N Engl J Med, 307 (1982), pp. 1131-1133
[10.]
A. Moryan, A.T. Guay, S. Kurtz, P.J. Nowak.
Familial ciliary dyskinesis. A cause of infertility without respiratory disease.
Fertil Steril, 44 (1985), pp. 539-542
[11.]
M. Greenstone, A. Dewar, P.J. Cole.
Ciliary dyskinesia with normal ultraestructure.
Thorax, 38 (1983), pp. 875-876
[12.]
M. Greenstone, A. Rutman, D. Pavia, D. Lawrence, P.J. Cole.
Normal axonemal structure and function in Kartagener's syndrome: an inexplicable paradox.
Thorax, 40 (1985), pp. 956-957
[13.]
E. Escudier, D. Escalier, J.P. Thomasson, M.C. Pinchon, J.F. Bernardin.
Unexpectedly normal cilia and spermatozoa in an infertile man with Kartagener's syndrome.
Eur Respir J, 70 (1987), pp. 180-186
[14.]
C.W.B. Corkey, H. Levison, J.A.P. Turner.
The inmotile cilia syndrome. A longitudinal survey.
Am Rev Respir Dis, 124 (1981), pp. 544-548
[15.]
A. Ellerman, H. Biggaard.
Longitudinal study of lung function in a cohort of primary ciliary dyskinesia.
Eur Respir J, 10 (1997), pp. 2376-2379
[16.]
M.J. Barranco, M. Armengot, C. Cardá, M.A. Císcar, B. Peris, M. Ramón, et al.
Síndrome de discinesia ciliar primaria Una patología frecuente..
Arch Bronconeumol, 30 (1994), pp. 19-22
[17.]
R. Jahrsdoerfer, P.S. Feldman, E.W. Rubel, J.L. Guerrant, P.A. Eggleston, R.F. Selden.
Otitis media and the immotile cilia syndrome.
Laryngoscope, 89 (1979), pp. 769-778
[18.]
L.A. Smallman, J. Gregory.
Ultraestructural abnormalities of cilia in the human respiratory tract.
Hum Pathol, 17 (1986), pp. 848-855
[19.]
G. Lungarella, L. Fonzi, G. Ermini.
Abnormalities of bronchial cilia in patients with chronic bronchitis An structural and quantitative analysis..
Lung, 161 (1983), pp. 147-156
[20.]
B.K. Rubin.
Inmotile cilia syndrome (primary ciliary diskinesia) and inflammatory lung disease.
Clin Chest Med, 9 (1988), pp. 657-668
[21.]
R. Jolis, J. Sauret, J. Corominas, R. Cornudella.
Determinación del aclaramiento mucociliar nasal mediante el test de la sacarina en diversas enfermedades respiratorias.
Arch Bronconeumol, 28 (1992), pp. 217-220
Copyright © 2000. Sociedad Española de Neumología y Cirugía Torácica
Archivos de Bronconeumología
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