2011, Number 2
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Rev Cent Dermatol Pascua 2011; 20 (2)
Progressive symmetric erythokeratodermia
Morales BME, Marín HE, Orellana AÁR, Villagómez LE, Peralta CG
Language: Spanish
References: 18
Page: 59-62
PDF size: 349.18 Kb.
ABSTRACT
Progressive symmetric Erythrokeratodermia (PSEQ) is a genodermatosis characterized by large polycyclic and hyperkeratotic plaques, fixed in location, symmetrically distributed mainly on the limbs.
In this article we present four cases with SEQ, three of them are relatives and the last one sporadic, and we made a review of the literature.
REFERENCES
Wolff K, Goldsmith L, Katz S et al. Fitzpatrick`s Dermatology in General Medicine. 7th Ed. E.U. Mc Graw-Hill 2008:417-418.
Richard G, Ringpfeil F. Ichthyoses, erythrokeratodermas and related disorders. In: Bolognia JL, Jorizzo JL, Rapini R, editors. Dermatology, 2nd ed. E.U. Mosby Elsevier 2008; 56: 800-801.
Bottegal H, García R, Cervini A et al. Eritroqueratodermia simétrica progresiva: síndrome de Gottron. Arch Argent Dermatol 2000; 50: 67-73.
Ishida-Yamamoto A, McGrath J, Lam H et al. The molecular pathology of progressive symmetric erythrokeratoderma: a frame shift mutation in the loricrin gene and perturbations in the cornified cell envelope. Am J Hum Genet 1997; 61: 581-589.
Ishida-Yamamoto A, Tanaka H, Takahashi H et al. Programmed cell death in normal epidermis and loricrin keratoderma. Multiple functions of profilaggrin in keratinization. J Investig Dermatol Symp Proc 1999; 4: 145-149.
Cui Y, Yang S, Gao M et al. Identification of a novel locus for progressive symmetric erythrokeratodermia to a 19.02-cM interval at 21q11.2-21q21.2. J Invest Dermatol 2006; 126: 2136-2139.
Koch P, Viragh P, Scharer E et al. Lessons from loricrin-deficient mice compensatory mechanisms maintaining skin barrier function in the absence of a major cornified envelope protein. J Cell Biol 2000; 151: 389-400.
Steensel M, Oranje A, Schroeff J et al. The missense mutation G12D in connexin 30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of Gottron. Am J Med Genet A 2009; 149: 657-661.
Morelli JG. Disorders of keratinization. In: Kliegman. Nelson Textbook of Pediatrics, 18th ed. E.U. Saunders 2007; 657.
Eichenfield L. Erythrokeratoderma progressive symmetrica disorders of cornification (Ichthyosis). Neonatal Dermatology, 2nd ed. Elsevier Saunders, 2008; 232.
Rodero J, Torrelo A, Mediero I et al. Eritroqueratodermia simétrica progresiva generalizada. Actas Dermosifiliográficas 2001; 92: 207-209.
Raza N. Progressive symmetrical erythrokeratoderma with perioral involvement. J Coll Physicians Surg Pack 2006; 16: 729-731.
Miura Y, Yoshiike T, Sou H, Yaguchi H, Ogawa H. A case report of progressive symmetric erythrokeratodermia and a review of progressive erythrokeratodermia in Japan. Japanese Journal of Dermatology 1991; 101: 635-643.
Zanini M, Bertino D, Correa K, Camargo L, Landaman G, Freitas E. Erythrokeratodermia simétrica progresiva: relato de um caso esporádico e de surgimento tardio. Med Cutan Iber Lat Am 2003; 31: 192-194.
Dal Magro C, Pellenz C, Bakos L. Eritroqueratodermia simétrica progressiva: relato de un caso. An Bras Dermatol 2003; 78: 587-591.
Khoo B, Tay Y, Tan S. Generalized erythematous plaques. Arch of Dermatol 2000; 136: 665-670.
Kiesewetter F, Simon M Jr, Fartasch M, Gevatter M. Progressive partially symmetric erythrokeratodermia with deafness: histological and ultrastructural evidence for a subtype distinct from Schnyder’s syndrome. Dermatology 1993; 186: 222-225.
Ott H, Lehmann S, Poblete-Gutierrez P, Frank J. Progressive symmetrische erythrokeratodermie Darier-Gottron. Der Hautarzt 2004; 55: 994-996.