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Vol. 99. Núm. 6.
Páginas 481-484 (agosto 2008)
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Vol. 99. Núm. 6.
Páginas 481-484 (agosto 2008)
Case reports
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Exacerbation of Skin Lesions During Fever in a Patient With Chronic Infantile Neurologic Cutaneous Articular Syndrome
Síndrome Cinca: Presentación de un Caso Con Exacerbación Febril de Sus Lesiones Cutáneas
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S. Aboín-Gonzáleza,
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asonsoles@hotmail.com

Correspondence: Servicio de Dermatología, Hospital Ramón y Cajal Universidad de Alcalá de Henares, Carretera de Colmenar Viejo, km 9,400, 28034 Madrid, Spain.
, I. Aldanondo-Fernández de la Moraa, C.R. García-Acebesa, R. Carrillo-Gijónb, A. Harto-Castañoa, P. Jaén-Olasoloa
a Servicio de Dermatología, Hospital Ramón y Cajal, Universidad de Alcalá de Henares, Madrid, Spain
b Servicio de Anatomía Patológica, Hospital Ramón y Cajal, Universidad de Alcalá de Henares, Madrid, Spain
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Abstract

Chronic infantile neurologic cutaneous articular (CINCA) syndrome is a serious chronic systemic inflammatory disease that presents at a young age and that is characterized by skin, joint, and central nervous system disease. Skin symptoms are the first to appear, in the form of a longstanding nonpruritic urticarial rash, with exacerbations coinciding with episodes of fever, arthritis, and enlarged lymph nodes. The findings of biopsy of skin lesions are extremely variable but characterized by perivascular neutrophilic infiltrate. With the discovery of mutations in the CIAS1 gene, which encodes a protein known as cryopyrin, this entity has been classified as one of the cryopyrin-associated autoinflammatory diseases, along with familial cold urticaria and Muckle-Wells syndrome. This discovery has also made available new therapeutic options. We present the case of a boy diagnosed with CINCA syndrome who presented with an outbreak of painful skin lesions and fever. These lesions were thought to be an exacerbation of underlying lesions during an episode of fever.

Key words:
chronic infantile neurologic cutaneous and articular syndrome
neonatal onset multi-inflammatory disease
neutrophilic dermatitis
cryopyrin
Resumen

El síndrome CINCA (Chronic Infantile Neurologic Cutaneous Articular Syndrome) es una grave enfermedad inflamatoria sistémica crónica, de instauración temprana, que se caracteriza por afectación cutánea, articular y del sistema nervioso central (SNC). La clínica cutánea en forma de exantema urticariforme no pruriginoso es la primera en aparecer, siendo más o menos permanente con exacerbaciones que coinciden con brotes de fiebre, artritis y adenopatías. La biopsia de las lesiones cutáneas es muy variable, aunque destaca un infiltrado neutrofílico perivascular. El descubrimiento de mutaciones en el gen CIAS1, que codifica una proteína llamada criopirina, ha permitido añadir esta entidad al espectro de las enfermedades autoinflamatorias asociadas a criopirinas, junto con la urticaria familiar por frío y el síndrome de Muckle-Wells, implicando además nuevas opciones terapéuticas. Presentamos el caso de un varón diagnosticado de síndrome CINCA que presentó un brote de lesiones cutáneas dolorosas y fiebre, interpretándose éstas como una exacerbación de sus lesiones habituales durante un episodio febril.

Palabras clave:
CINCA (Chronic Infantile Neurologic Cutaneous Articular Syndrome)
NOMID (Neonatal Onset Multi-Inflammatory Disease)
dermatitis neutrofílica
criopirina
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References
[1.]
A.M. Prieur, C. Griscelli, F. Lampert, H. Truckenbrodt, M.A. Guggenheim, D.J. Lovell, et al.
A chronic infantile, neurological, cutaneous and articular (CINCA) syndrome. A specific entity analysed in 30 patients.
Scand J Rheumatol Suppl, 66 (1987), pp. 57-68
[2.]
F.I. Mongil, V. Canduela.
Fiebre periódica.
An Esp Pediatr, 57 (2002), pp. 334-344
[3.]
A.M. Prieur.
A recently recognized chronic inflammatory disease of early onset characterized by the triad of rash, central nervous system involvement and arthropathy.
Clin Exp Rheumatol, 19 (2001), pp. 403-406
[4.]
J. Feldmann, A.M. Prieur, P. Quartier, P. Berquin, S. Certain, E. Cortis, et al.
Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes.
Am J Hum Genet, 71 (2002), pp. 198-203
[5.]
I. Aksentijevich, M. Nowak, M. Mallah, J.J. Chae, W.T. Watford, S.R. Hofmann, et al.
De novo CIAS1 mutations cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID).
Arthritis Rheum, 46 (2002), pp. 3340-3348
[6.]
A.M. Prieur, C. Griscelli.
Arthropathy with rash, chronic meningitis, eye lesions and mental retardation.
J Pediatr, 99 (1981), pp. 79-83
[7.]
S.G. Hassink, D.P. Goldsmith.
Neonatal onset multisystem inflammatory disease.
Arthritis Rheum, 26 (1983), pp. 668-673
[8.]
V. Leone, G. Presani, S. Perticarari, A. Tommasini, S. Crovella, A. Lenhardt, et al.
Chronic infantile neurological cutaneous articular syndrome: CD10 over expression in neutrophils is a possible key to the pathogenesis of the disease.
Eur J Pediatr, 162 (2003), pp. 669-673
[9.]
H. De Boeck, T. Scheerlinck, J. Otten.
The CINCA syndrome: a rare cause of chronic arthritis and multisystem inflammatory disorders.
Acta Orthop Belg, 66 (2000), pp. 433-437
[10.]
K.M. Hull, N. Shoham, J.J. Chae, I. Aksentijevich, D.L. Kastner.
The expanding spectrum of systemic autoinflammatory disorders and their rheumatic manifestations.
Curr Opin Rheumatol, 15 (2003), pp. 61-69
[11.]
B. Granel, N. Philip, J. Serratrice, N. Ene, G. Grateau, C. Dodé, et al.
CIAS1 mutation in a patient with overlap between Muckle-Wells and chronic infantile neurological cutaneous and articular syndromes.
Dermatology, 206 (2003), pp. 257-259
[12.]
V. Hentgen, V. Despert, A.C. Lepretre, L. Cuisset, J. Chevrant-Breton, P. Jego, et al.
Intrafamilial variable phenotypic expression of a CIAS1 mutation: from Muckle-Wells to chronic infantile neurological cutaneous and articular syndrome.
J Rheumatol, 32 (2005), pp. 747-751
[13.]
H.M. Hoffman, J.L. Mueller, D.H. Broide, A.A. Wanderer, R.D. Kolodner.
Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome.
Nature Genet, 29 (2001), pp. 301-305
[14.]
C. Kilcline, K. Shinkai, A. Bree, R. Modica, E. Von Scheven, I.J. Frieden.
Neonatal onset multisystem inflammatory disorder: the emerging role of pyrin genes in autoinflammatory diseases.
Arch Dermatol, 141 (2005), pp. 248-253
[15.]
R. Goldbach-Mansky, N.J. Daily, S.W. Canna, A. Gelabert, J. Jones, B.I. Rubin, et al.
Neonatal-onset multisystem inflammatory disease responsive to interleukin-Ibeta Inhibition.
N Engl J Med, 355 (2006), pp. 646-647
[16.]
D.J. Lovell, S.L. Bowyer, A.M. Solinger.
Interleukin-1 blockade by anakinra improves clinical and symptoms in patients with neonatal onset multisystem inflammatory disease.
Arthritis Rheum, 52 (2005), pp. 183-184
[17.]
Jl. Callejas, J. Oliver, J. Martín, N. Ortego.
Anakinra in mutationnegative CINCA syndrome.
Clin Rheumatol, 26 (2007), pp. 576-577
Copyright © 2008. Academia Española de Dermatología y Venereología and Elsevier España, S.L.
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